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Wyszukujesz frazę ""Hakonarson H"" wg kryterium: Autor


Tytuł:
A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations.
Autorzy:
Bønnelykke K; 1] Copenhagen Prospective Studies on Asthma in Childhood, Health Sciences, University of Copenhagen & Danish Pediatric Asthma Center, Copenhagen University Hospital, Gentofte, Denmark. [2] [3].
Sleiman P; 1] Center for Applied Genomics, Children's Hospital of Philadelphia (CHOP), Philadelphia, Pennsylvania, USA. [2].
Nielsen K; 1] Center for Biological Sequence Analysis, Department of Systems Biology, Technical University of Denmark, Lyngby, Denmark. [2].
Kreiner-Møller E; Copenhagen Prospective Studies on Asthma in Childhood, Health Sciences, University of Copenhagen & Danish Pediatric Asthma Center, Copenhagen University Hospital, Gentofte, Denmark.
Mercader JM; Joint Institute for Research in Biomedicine and Barcelona Supercomputing Center (IRB-BSC) Program on Computational Biology, Barcelona Supercomputing Center, Barcelona, Spain.
Belgrave D; 1] Centre for Respiratory Medicine and Allergy, Institute of Inflammation and Repair, University of Manchester and University Hospital of South Manchester, Manchester, UK. [2] Centre for Health Informatics, Institute of Population Health, University of Manchester, Manchester, UK.
den Dekker HT; 1] Generation R Study Group, Erasmus Medical Center, Rotterdam, The Netherlands. [2] Department of Pediatrics, Division of Respiratory Medicine, Erasmus Medical Center, Rotterdam, The Netherlands. [3] Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.
Husby A; 1] Copenhagen Prospective Studies on Asthma in Childhood, Health Sciences, University of Copenhagen & Danish Pediatric Asthma Center, Copenhagen University Hospital, Gentofte, Denmark. [2] Brooke Laboratory, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, University Hospital Southampton, Southampton, UK.
Sevelsted A; Copenhagen Prospective Studies on Asthma in Childhood, Health Sciences, University of Copenhagen & Danish Pediatric Asthma Center, Copenhagen University Hospital, Gentofte, Denmark.
Faura-Tellez G; 1] Faculty of Medicine, University of Southampton, Southampton General Hospital, Southampton, UK. [2] Pediatric Pulmonology and Pediatric Allergology, University of Groningen, University Medical Center Groningen, Beatrix Children's Hospital, Groningen Research Institute for Asthma and COPD, Groningen, The Netherlands.
Mortensen LJ; Copenhagen Prospective Studies on Asthma in Childhood, Health Sciences, University of Copenhagen & Danish Pediatric Asthma Center, Copenhagen University Hospital, Gentofte, Denmark.
Paternoster L; Integrative Epidemiology Unit, School of Social & Community Medicine, University of Bristol, Bristol, UK.
Flaaten R; Copenhagen Prospective Studies on Asthma in Childhood, Health Sciences, University of Copenhagen & Danish Pediatric Asthma Center, Copenhagen University Hospital, Gentofte, Denmark.
Mølgaard A; Copenhagen Prospective Studies on Asthma in Childhood, Health Sciences, University of Copenhagen & Danish Pediatric Asthma Center, Copenhagen University Hospital, Gentofte, Denmark.
Smart DE; Brooke Laboratory, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, University Hospital Southampton, Southampton, UK.
Thomsen PF; Center for GeoGenetics, Natural History Museum of Denmark, University of Copenhagen, Copenhagen, Denmark.
Rasmussen MA; Department of Food Science, University of Copenhagen, Copenhagen, Denmark.
Bonàs-Guarch S; Joint Institute for Research in Biomedicine and Barcelona Supercomputing Center (IRB-BSC) Program on Computational Biology, Barcelona Supercomputing Center, Barcelona, Spain.
Holst C; Institute of Preventive Medicine, Copenhagen University Hospital, Copenhagen, Denmark.
Nohr EA; 1] Institute of Clinical Research, University of Southern Denmark, Aarhus, Denmark. [2] Department of Public Health, Section for Epidemiology, Aarhus University, Aarhus, Denmark.
Yadav R; Center for Biological Sequence Analysis, Department of Systems Biology, Technical University of Denmark, Lyngby, Denmark.
March ME; Center for Applied Genomics, Children's Hospital of Philadelphia (CHOP), Philadelphia, Pennsylvania, USA.
Blicher T; Novo Nordisk Foundation Center for Protein Research, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.
Lackie PM; Faculty of Medicine, University of Southampton, Southampton General Hospital, Southampton, UK.
Jaddoe VW; 1] Generation R Study Group, Erasmus Medical Center, Rotterdam, The Netherlands. [2] Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands. [3] Department of Pediatrics, Erasmus Medical Center, Rotterdam, The Netherlands.
Simpson A; Centre for Respiratory Medicine and Allergy, Institute of Inflammation and Repair, University of Manchester and University Hospital of South Manchester, Manchester, UK.
Holloway JW; Faculty of Medicine, University of Southampton, Southampton General Hospital, Southampton, UK.
Duijts L; 1] Department of Pediatrics, Division of Respiratory Medicine, Erasmus Medical Center, Rotterdam, The Netherlands. [2] Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands. [3] Department of Pediatrics, Division of Neonatology, Erasmus Medical Center, Rotterdam, The Netherlands.
Custovic A; Centre for Respiratory Medicine and Allergy, Institute of Inflammation and Repair, University of Manchester and University Hospital of South Manchester, Manchester, UK.
Davies DE; Brooke Laboratory, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, University Hospital Southampton, Southampton, UK.
Torrents D; 1] Joint Institute for Research in Biomedicine and Barcelona Supercomputing Center (IRB-BSC) Program on Computational Biology, Barcelona Supercomputing Center, Barcelona, Spain. [2] Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona, Spain.
Gupta R; Center for Biological Sequence Analysis, Department of Systems Biology, Technical University of Denmark, Lyngby, Denmark.
Hollegaard MV; Danish Centre for Neonatal Screening, Department of Clinical Biochemistry and Immunology, Statens Serum Institut (SSI), Copenhagen, Denmark.
Hougaard DM; Danish Centre for Neonatal Screening, Department of Clinical Biochemistry and Immunology, Statens Serum Institut (SSI), Copenhagen, Denmark.
Hakonarson H; 1] Center for Applied Genomics, Children's Hospital of Philadelphia (CHOP), Philadelphia, Pennsylvania, USA. [2].
Bisgaard H; 1] Copenhagen Prospective Studies on Asthma in Childhood, Health Sciences, University of Copenhagen & Danish Pediatric Asthma Center, Copenhagen University Hospital, Gentofte, Denmark. [2].
Pokaż więcej
Źródło:
Nature genetics [Nat Genet] 2014 Jan; Vol. 46 (1), pp. 51-5. Date of Electronic Publication: 2013 Nov 17.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Predisposition to Disease*
Asthma/*genetics
Cadherins/*genetics
Membrane Proteins/*genetics
Acid Anhydride Hydrolases ; Asthma/etiology ; Cadherin Related Proteins ; Cadherins/chemistry ; Cadherins/metabolism ; Case-Control Studies ; Child ; Child, Preschool ; Chromosomes, Human, Pair 17 ; DNA Repair Enzymes/genetics ; DNA-Binding Proteins/genetics ; Denmark ; Female ; Genome-Wide Association Study ; Humans ; Interleukin-1 Receptor-Like 1 Protein ; Interleukin-33 ; Interleukins/genetics ; Male ; Membrane Proteins/chemistry ; Membrane Proteins/metabolism ; Models, Molecular ; Neoplasm Proteins/genetics ; Polymorphism, Single Nucleotide ; Protein Conformation ; Receptors, Cell Surface/genetics
Czasopismo naukowe
Tytuł:
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.
Autorzy:
Lambert JC
Ibrahim-Verbaas CA
Harold D
Naj AC
Sims R
Bellenguez C
DeStafano AL
Bis JC
Beecham GW
Grenier-Boley B
Russo G
Thorton-Wells TA
Jones N
Smith AV
Chouraki V
Thomas C
Ikram MA
Zelenika D
Vardarajan BN
Kamatani Y
Lin CF
Gerrish A
Schmidt H
Kunkle B
Dunstan ML
Ruiz A
Bihoreau MT
Choi SH
Reitz C
Pasquier F
Cruchaga C
Craig D
Amin N
Berr C
Lopez OL
De Jager PL
Deramecourt V
Johnston JA
Evans D
Lovestone S
Letenneur L
Morón FJ
Rubinsztein DC
Eiriksdottir G
Sleegers K
Goate AM
Fiévet N
Huentelman MW
Gill M
Brown K
Kamboh MI
Keller L
Barberger-Gateau P
McGuiness B
Larson EB
Green R
Myers AJ
Dufouil C
Todd S
Wallon D
Love S
Rogaeva E
Gallacher J
St George-Hyslop P
Clarimon J
Lleo A
Bayer A
Tsuang DW
Yu L
Tsolaki M
Bossù P
Spalletta G
Proitsi P
Collinge J
Sorbi S
Sanchez-Garcia F
Fox NC
Hardy J
Deniz Naranjo MC
Bosco P
Clarke R
Brayne C
Galimberti D
Mancuso M
Matthews F
Moebus S
Mecocci P
Del Zompo M
Maier W
Hampel H
Pilotto A
Bullido M
Panza F
Caffarra P
Nacmias B
Gilbert JR
Mayhaus M
Lannefelt L
Hakonarson H
Pichler S
Carrasquillo MM
Ingelsson M
Beekly D
Alvarez V
Zou F
Valladares O
Younkin SG
Coto E
Hamilton-Nelson KL
Gu W
Razquin C
Pastor P
Mateo I
Owen MJ
Faber KM
Jonsson PV
Combarros O
O'Donovan MC
Cantwell LB
Soininen H
Blacker D
Mead S
Mosley TH Jr
Bennett DA
Harris TB
Fratiglioni L
Holmes C
de Bruijn RF
Passmore P
Montine TJ
Bettens K
Rotter JI
Brice A
Morgan K
Foroud TM
Kukull WA
Hannequin D
Powell JF
Nalls MA
Ritchie K
Lunetta KL
Kauwe JS
Boerwinkle E
Riemenschneider M
Boada M
Hiltuenen M
Martin ER
Schmidt R
Rujescu D
Wang LS
Dartigues JF
Mayeux R
Tzourio C
Hofman A
Nöthen MM
Graff C
Psaty BM
Jones L
Haines JL
Holmans PA
Lathrop M
Pericak-Vance MA
Launer LJ
Farrer LA
van Duijn CM
Van Broeckhoven C
Moskvina V
Seshadri S
Williams J
Schellenberg GD
Amouyel P
Pokaż więcej
Corporate Authors:
European Alzheimer's Disease Initiative (EADI)
Genetic and Environmental Risk in Alzheimer's Disease
Alzheimer's Disease Genetic Consortium
Cohorts for Heart and Aging Research in Genomic Epidemiology
Źródło:
Nature genetics [Nat Genet] 2013 Dec; Vol. 45 (12), pp. 1452-8. Date of Electronic Publication: 2013 Oct 27.
Typ publikacji:
Journal Article; Meta-Analysis; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Loci*
Genetic Predisposition to Disease*
Alzheimer Disease/*genetics
Genome-Wide Association Study/*statistics & numerical data
Age of Onset ; Aged ; Aged, 80 and over ; Alzheimer Disease/epidemiology ; Case-Control Studies ; Cohort Studies ; Female ; Humans ; Male ; Middle Aged ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Tytuł:
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.
Autorzy:
Beecham AH
Patsopoulos NA
Xifara DK
Davis MF
Kemppinen A
Cotsapas C
Shah TS
Spencer C
Booth D
Goris A
Oturai A
Saarela J
Fontaine B
Hemmer B
Martin C
Zipp F
D'Alfonso S
Martinelli-Boneschi F
Taylor B
Harbo HF
Kockum I
Hillert J
Olsson T
Ban M
Oksenberg JR
Hintzen R
Barcellos LF
Agliardi C
Alfredsson L
Alizadeh M
Anderson C
Andrews R
Søndergaard HB
Baker A
Band G
Baranzini SE
Barizzone N
Barrett J
Bellenguez C
Bergamaschi L
Bernardinelli L
Berthele A
Biberacher V
Binder TM
Blackburn H
Bomfim IL
Brambilla P
Broadley S
Brochet B
Brundin L
Buck D
Butzkueven H
Caillier SJ
Camu W
Carpentier W
Cavalla P
Celius EG
Coman I
Comi G
Corrado L
Cosemans L
Cournu-Rebeix I
Cree BA
Cusi D
Damotte V
Defer G
Delgado SR
Deloukas P
di Sapio A
Dilthey AT
Donnelly P
Dubois B
Duddy M
Edkins S
Elovaara I
Esposito F
Evangelou N
Fiddes B
Field J
Franke A
Freeman C
Frohlich IY
Galimberti D
Gieger C
Gourraud PA
Graetz C
Graham A
Grummel V
Guaschino C
Hadjixenofontos A
Hakonarson H
Halfpenny C
Hall G
Hall P
Hamsten A
Harley J
Harrower T
Hawkins C
Hellenthal G
Hillier C
Hobart J
Hoshi M
Hunt SE
Jagodic M
Jelčić I
Jochim A
Kendall B
Kermode A
Kilpatrick T
Koivisto K
Konidari I
Korn T
Kronsbein H
Langford C
Larsson M
Lathrop M
Lebrun-Frenay C
Lechner-Scott J
Lee MH
Leone MA
Leppä V
Liberatore G
Lie BA
Lill CM
Lindén M
Link J
Luessi F
Lycke J
Macciardi F
Männistö S
Manrique CP
Martin R
Martinelli V
Mason D
Mazibrada G
McCabe C
Mero IL
Mescheriakova J
Moutsianas L
Myhr KM
Nagels G
Nicholas R
Nilsson P
Piehl F
Pirinen M
Price SE
Quach H
Reunanen M
Robberecht W
Robertson NP
Rodegher M
Rog D
Salvetti M
Schnetz-Boutaud NC
Sellebjerg F
Selter RC
Schaefer C
Shaunak S
Shen L
Shields S
Siffrin V
Slee M
Sorensen PS
Sorosina M
Sospedra M
Spurkland A
Strange A
Sundqvist E
Thijs V
Thorpe J
Ticca A
Tienari P
van Duijn C
Visser EM
Vucic S
Westerlind H
Wiley JS
Wilkins A
Wilson JF
Winkelmann J
Zajicek J
Zindler E
Haines JL
Pericak-Vance MA
Ivinson AJ
Stewart G
Hafler D
Hauser SL
Compston A
McVean G
De Jager P
Sawcer SJ
McCauley JL
Pokaż więcej
Corporate Authors:
International Multiple Sclerosis Genetics Consortium (IMSGC); 1] John P. Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, Miami, Florida, USA. [2].
Wellcome Trust Case Control Consortium 2 (WTCCC2)
International IBD Genetics Consortium (IIBDGC)
Źródło:
Nature genetics [Nat Genet] 2013 Nov; Vol. 45 (11), pp. 1353-60. Date of Electronic Publication: 2013 Sep 29.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Multiple Sclerosis/*genetics
Multiple Sclerosis/*immunology
Chromosome Mapping ; Gene Frequency ; Genetic Loci ; Genetic Predisposition to Disease ; Genetic Variation ; Genome-Wide Association Study ; Genotype ; Humans ; Polymorphism, Single Nucleotide ; White People/genetics
Czasopismo naukowe
Tytuł:
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
Autorzy:
Lee SH
Ripke S
Neale BM
Faraone SV
Purcell SM
Perlis RH
Mowry BJ
Thapar A
Goddard ME
Witte JS
Absher D
Agartz I
Akil H
Amin F
Andreassen OA
Anjorin A
Anney R
Anttila V
Arking DE
Asherson P
Azevedo MH
Backlund L
Badner JA
Bailey AJ
Banaschewski T
Barchas JD
Barnes MR
Barrett TB
Bass N
Battaglia A
Bauer M
Bayés M
Bellivier F
Bergen SE
Berrettini W
Betancur C
Bettecken T
Biederman J
Binder EB
Black DW
Blackwood DH
Bloss CS
Boehnke M
Boomsma DI
Breen G
Breuer R
Bruggeman R
Cormican P
Buccola NG
Buitelaar JK
Bunney WE
Buxbaum JD
Byerley WF
Byrne EM
Caesar S
Cahn W
Cantor RM
Casas M
Chakravarti A
Chambert K
Choudhury K
Cichon S
Cloninger CR
Collier DA
Cook EH
Coon H
Cormand B
Corvin A
Coryell WH
Craig DW
Craig IW
Crosbie J
Cuccaro ML
Curtis D
Czamara D
Datta S
Dawson G
Day R
De Geus EJ
Degenhardt F
Djurovic S
Donohoe GJ
Doyle AE
Duan J
Dudbridge F
Duketis E
Ebstein RP
Edenberg HJ
Elia J
Ennis S
Etain B
Fanous A
Farmer AE
Ferrier IN
Flickinger M
Fombonne E
Foroud T
Frank J
Franke B
Fraser C
Freedman R
Freimer NB
Freitag CM
Friedl M
Frisén L
Gallagher L
Gejman PV
Georgieva L
Gershon ES
Geschwind DH
Giegling I
Gill M
Gordon SD
Gordon-Smith K
Green EK
Greenwood TA
Grice DE
Gross M
Grozeva D
Guan W
Gurling H
De Haan L
Haines JL
Hakonarson H
Hallmayer J
Hamilton SP
Hamshere ML
Hansen TF
Hartmann AM
Hautzinger M
Heath AC
Henders AK
Herms S
Hickie IB
Hipolito M
Hoefels S
Holmans PA
Holsboer F
Hoogendijk WJ
Hottenga JJ
Hultman CM
Hus V
Ingason A
Ising M
Jamain S
Jones EG
Jones I
Jones L
Tzeng JY
Kähler AK
Kahn RS
Kandaswamy R
Keller MC
Kennedy JL
Kenny E
Kent L
Kim Y
Kirov GK
Klauck SM
Klei L
Knowles JA
Kohli MA
Koller DL
Konte B
Korszun A
Krabbendam L
Krasucki R
Kuntsi J
Kwan P
Landén M
Långström N
Lathrop M
Lawrence J
Lawson WB
Leboyer M
Ledbetter DH
Lee PH
Lencz T
Lesch KP
Levinson DF
Lewis CM
Li J
Lichtenstein P
Lieberman JA
Lin DY
Linszen DH
Liu C
Lohoff FW
Loo SK
Lord C
Lowe JK
Lucae S
MacIntyre DJ
Madden PA
Maestrini E
Magnusson PK
Mahon PB
Maier W
Malhotra AK
Mane SM
Martin CL
Martin NG
Mattheisen M
Matthews K
Mattingsdal M
McCarroll SA
McGhee KA
McGough JJ
McGrath PJ
McGuffin P
McInnis MG
McIntosh A
McKinney R
McLean AW
McMahon FJ
McMahon WM
McQuillin A
Medeiros H
Medland SE
Meier S
Melle I
Meng F
Meyer J
Middeldorp CM
Middleton L
Milanova V
Miranda A
Monaco AP
Montgomery GW
Moran JL
Moreno-De-Luca D
Morken G
Morris DW
Morrow EM
Moskvina V
Muglia P
Mühleisen TW
Muir WJ
Müller-Myhsok B
Murtha M
Myers RM
Myin-Germeys I
Neale MC
Nelson SF
Nievergelt CM
Nikolov I
Nimgaonkar V
Nolen WA
Nöthen MM
Nurnberger JI
Nwulia EA
Nyholt DR
O'Dushlaine C
Oades RD
Olincy A
Oliveira G
Olsen L
Ophoff RA
Osby U
Owen MJ
Palotie A
Parr JR
Paterson AD
Pato CN
Pato MT
Penninx BW
Pergadia ML
Pericak-Vance MA
Pickard BS
Pimm J
Piven J
Posthuma D
Potash JB
Poustka F
Propping P
Puri V
Quested DJ
Quinn EM
Ramos-Quiroga JA
Rasmussen HB
Raychaudhuri S
Rehnström K
Reif A
Ribasés M
Rice JP
Rietschel M
Roeder K
Roeyers H
Rossin L
Rothenberger A
Rouleau G
Ruderfer D
Rujescu D
Sanders AR
Sanders SJ
Santangelo SL
Sergeant JA
Schachar R
Schalling M
Schatzberg AF
Scheftner WA
Schellenberg GD
Scherer SW
Schork NJ
Schulze TG
Schumacher J
Schwarz M
Scolnick E
Scott LJ
Shi J
Shilling PD
Shyn SI
Silverman JM
Slager SL
Smalley SL
Smit JH
Smith EN
Sonuga-Barke EJ
St Clair D
State M
Steffens M
Steinhausen HC
Strauss JS
Strohmaier J
Stroup TS
Sutcliffe JS
Szatmari P
Szelinger S
Thirumalai S
Thompson RC
Todorov AA
Tozzi F
Treutlein J
Uhr M
van den Oord EJ
Van Grootheest G
Van Os J
Vicente AM
Vieland VJ
Vincent JB
Visscher PM
Walsh CA
Wassink TH
Watson SJ
Weissman MM
Werge T
Wienker TF
Wijsman EM
Willemsen G
Williams N
Willsey AJ
Witt SH
Xu W
Young AH
Yu TW
Zammit S
Zandi PP
Zhang P
Zitman FG
Zöllner S
Devlin B
Kelsoe JR
Sklar P
Daly MJ
O'Donovan MC
Craddock N
Sullivan PF
Smoller JW
Kendler KS
Wray NR
Pokaż więcej
Corporate Authors:
Cross-Disorder Group of the Psychiatric Genomics Consortium; The University of Queensland, Queensland Brain Institute, Brisbane, Queensland, Australia.
International Inflammatory Bowel Disease Genetics Consortium (IIBDGC)
Źródło:
Nature genetics [Nat Genet] 2013 Sep; Vol. 45 (9), pp. 984-94. Date of Electronic Publication: 2013 Aug 11.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Predisposition to Disease*
Genome-Wide Association Study*
Polymorphism, Single Nucleotide*
Mental Disorders/*genetics
Adult ; Attention Deficit Disorder with Hyperactivity/genetics ; Bipolar Disorder/genetics ; Child ; Child Development Disorders, Pervasive/genetics ; Crohn Disease/genetics ; Depressive Disorder, Major/genetics ; Genetic Heterogeneity ; Genome, Human ; Humans ; Inheritance Patterns ; Schizophrenia/genetics
Czasopismo naukowe
Tytuł:
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry.
Autorzy:
Monda KL; The Center for Observational Research, Amgen, Inc. Thousand Oaks, California, USA.
Chen GK
Taylor KC
Palmer C
Edwards TL
Lange LA
Ng MC
Adeyemo AA
Allison MA
Bielak LF
Chen G
Graff M
Irvin MR
Rhie SK
Li G
Liu Y
Liu Y
Lu Y
Nalls MA
Sun YV
Wojczynski MK
Yanek LR
Aldrich MC
Ademola A
Amos CI
Bandera EV
Bock CH
Britton A
Broeckel U
Cai Q
Caporaso NE
Carlson CS
Carpten J
Casey G
Chen WM
Chen F
Chen YD
Chiang CW
Coetzee GA
Demerath E
Deming-Halverson SL
Driver RW
Dubbert P
Feitosa MF
Feng Y
Freedman BI
Gillanders EM
Gottesman O
Guo X
Haritunians T
Harris T
Harris CC
Hennis AJ
Hernandez DG
McNeill LH
Howard TD
Howard BV
Howard VJ
Johnson KC
Kang SJ
Keating BJ
Kolb S
Kuller LH
Kutlar A
Langefeld CD
Lettre G
Lohman K
Lotay V
Lyon H
Manson JE
Maixner W
Meng YA
Monroe KR
Morhason-Bello I
Murphy AB
Mychaleckyj JC
Nadukuru R
Nathanson KL
Nayak U
N'diaye A
Nemesure B
Wu SY
Leske MC
Neslund-Dudas C
Neuhouser M
Nyante S
Ochs-Balcom H
Ogunniyi A
Ogundiran TO
Ojengbede O
Olopade OI
Palmer JR
Ruiz-Narvaez EA
Palmer ND
Press MF
Rampersaud E
Rasmussen-Torvik LJ
Rodriguez-Gil JL
Salako B
Schadt EE
Schwartz AG
Shriner DA
Siscovick D
Smith SB
Wassertheil-Smoller S
Speliotes EK
Spitz MR
Sucheston L
Taylor H
Tayo BO
Tucker MA
Van Den Berg DJ
Edwards DR
Wang Z
Wiencke JK
Winkler TW
Witte JS
Wrensch M
Wu X
Yang JJ
Levin AM
Young TR
Zakai NA
Cushman M
Zanetti KA
Zhao JH
Zhao W
Zheng Y
Zhou J
Ziegler RG
Zmuda JM
Fernandes JK
Gilkeson GS
Kamen DL
Hunt KJ
Spruill IJ
Ambrosone CB
Ambs S
Arnett DK
Atwood L
Becker DM
Berndt SI
Bernstein L
Blot WJ
Borecki IB
Bottinger EP
Bowden DW
Burke G
Chanock SJ
Cooper RS
Ding J
Duggan D
Evans MK
Fox C
Garvey WT
Bradfield JP
Hakonarson H
Grant SF
Hsing A
Chu L
Hu JJ
Huo D
Ingles SA
John EM
Jordan JM
Kabagambe EK
Kardia SL
Kittles RA
Goodman PJ
Klein EA
Kolonel LN
Le Marchand L
Liu S
McKnight B
Millikan RC
Mosley TH
Padhukasahasram B
Williams LK
Patel SR
Peters U
Pettaway CA
Peyser PA
Psaty BM
Redline S
Rotimi CN
Rybicki BA
Sale MM
Schreiner PJ
Signorello LB
Singleton AB
Stanford JL
Strom SS
Thun MJ
Vitolins M
Zheng W
Moore JH
Williams SM
Ketkar S
Zhu X
Zonderman AB
Kooperberg C
Papanicolaou GJ
Henderson BE
Reiner AP
Hirschhorn JN
Loos RJ
North KE
Haiman CA
Pokaż więcej
Corporate Authors:
NABEC Consortium
UKBEC Consortium
BioBank Japan Project
AGEN Consortium
Źródło:
Nature genetics [Nat Genet] 2013 Jun; Vol. 45 (6), pp. 690-6. Date of Electronic Publication: 2013 Apr 14.
Typ publikacji:
Journal Article; Meta-Analysis; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Body Mass Index*
Black or African American/*genetics
Obesity/*genetics
Case-Control Studies ; Gene Frequency ; Genetic Loci ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Humans ; Linkage Disequilibrium ; Obesity/ethnology ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Tytuł:
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.
Autorzy:
Horikoshi M; Oxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Oxford, UK.
Yaghootkar H
Mook-Kanamori DO
Sovio U
Taal HR
Hennig BJ
Bradfield JP
St Pourcain B
Evans DM
Charoen P
Kaakinen M
Cousminer DL
Lehtimäki T
Kreiner-Møller E
Warrington NM
Bustamante M
Feenstra B
Berry DJ
Thiering E
Pfab T
Barton SJ
Shields BM
Kerkhof M
van Leeuwen EM
Fulford AJ
Kutalik Z
Zhao JH
den Hoed M
Mahajan A
Lindi V
Goh LK
Hottenga JJ
Wu Y
Raitakari OT
Harder MN
Meirhaeghe A
Ntalla I
Salem RM
Jameson KA
Zhou K
Monies DM
Lagou V
Kirin M
Heikkinen J
Adair LS
Alkuraya FS
Al-Odaib A
Amouyel P
Andersson EA
Bennett AJ
Blakemore AI
Buxton JL
Dallongeville J
Das S
de Geus EJ
Estivill X
Flexeder C
Froguel P
Geller F
Godfrey KM
Gottrand F
Groves CJ
Hansen T
Hirschhorn JN
Hofman A
Hollegaard MV
Hougaard DM
Hyppönen E
Inskip HM
Isaacs A
Jørgensen T
Kanaka-Gantenbein C
Kemp JP
Kiess W
Kilpeläinen TO
Klopp N
Knight BA
Kuzawa CW
McMahon G
Newnham JP
Niinikoski H
Oostra BA
Pedersen L
Postma DS
Ring SM
Rivadeneira F
Robertson NR
Sebert S
Simell O
Slowinski T
Tiesler CM
Tönjes A
Vaag A
Viikari JS
Vink JM
Vissing NH
Wareham NJ
Willemsen G
Witte DR
Zhang H
Zhao J
Wilson JF
Stumvoll M
Prentice AM
Meyer BF
Pearson ER
Boreham CA
Cooper C
Gillman MW
Dedoussis GV
Moreno LA
Pedersen O
Saarinen M
Mohlke KL
Boomsma DI
Saw SM
Lakka TA
Körner A
Loos RJ
Ong KK
Vollenweider P
van Duijn CM
Koppelman GH
Hattersley AT
Holloway JW
Hocher B
Heinrich J
Power C
Melbye M
Guxens M
Pennell CE
Bønnelykke K
Bisgaard H
Eriksson JG
Widén E
Hakonarson H
Uitterlinden AG
Pouta A
Lawlor DA
Smith GD
Frayling TM
McCarthy MI
Grant SF
Jaddoe VW
Jarvelin MR
Timpson NJ
Prokopenko I
Freathy RM
Pokaż więcej
Corporate Authors:
Meta-Analyses of Glucose- and Insulin-related traits Consortium (MAGIC)
Early Growth Genetics (EGG) Consortium
Źródło:
Nature genetics [Nat Genet] 2013 Jan; Vol. 45 (1), pp. 76-82. Date of Electronic Publication: 2012 Dec 02.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
MeSH Terms:
Genetic Linkage*
Quantitative Trait Loci*
Birth Weight/*genetics
Body Height/*genetics
Fetal Development/*genetics
Adult ; Blood Pressure/genetics ; Diabetes Mellitus, Type 2/genetics ; Female ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Humans ; Infant, Newborn ; Male ; Meta-Analysis as Topic ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Tytuł:
Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma.
Autorzy:
Diskin SJ; Division of Oncology, Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Capasso M
Schnepp RW
Cole KA
Attiyeh EF
Hou C
Diamond M
Carpenter EL
Winter C
Lee H
Jagannathan J
Latorre V
Iolascon A
Hakonarson H
Devoto M
Maris JM
Pokaż więcej
Źródło:
Nature genetics [Nat Genet] 2012 Oct; Vol. 44 (10), pp. 1126-30. Date of Electronic Publication: 2012 Sep 02.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Polymorphism, Single Nucleotide*
DNA-Binding Proteins/*genetics
Neuroblastoma/*genetics
Ubiquitin-Protein Ligases/*genetics
Case-Control Studies ; Cell Line, Tumor ; Cell Proliferation ; Chromosomes, Human, Pair 6 ; Cohort Studies ; DNA-Binding Proteins/metabolism ; Gene Expression ; Gene Frequency ; Gene Knockdown Techniques ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Humans ; Infant ; Kaplan-Meier Estimate ; Linkage Disequilibrium ; Neuroblastoma/metabolism ; Neuroblastoma/mortality ; Oligonucleotide Array Sequence Analysis ; RNA Interference ; RNA-Binding Proteins ; Sequence Analysis, DNA ; Transcriptome ; Ubiquitin-Protein Ligases/metabolism
Czasopismo naukowe
Tytuł:
A genome-wide association meta-analysis identifies new childhood obesity loci.
Autorzy:
Bradfield JP; Center for Applied Genomics, Abramson Research Center, The Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Taal HR
Timpson NJ
Scherag A
Lecoeur C
Warrington NM
Hypponen E
Holst C
Valcarcel B
Thiering E
Salem RM
Schumacher FR
Cousminer DL
Sleiman PM
Zhao J
Berkowitz RI
Vimaleswaran KS
Jarick I
Pennell CE
Evans DM
St Pourcain B
Berry DJ
Mook-Kanamori DO
Hofman A
Rivadeneira F
Uitterlinden AG
van Duijn CM
van der Valk RJ
de Jongste JC
Postma DS
Boomsma DI
Gauderman WJ
Hassanein MT
Lindgren CM
Mägi R
Boreham CA
Neville CE
Moreno LA
Elliott P
Pouta A
Hartikainen AL
Li M
Raitakari O
Lehtimäki T
Eriksson JG
Palotie A
Dallongeville J
Das S
Deloukas P
McMahon G
Ring SM
Kemp JP
Buxton JL
Blakemore AI
Bustamante M
Guxens M
Hirschhorn JN
Gillman MW
Kreiner-Møller E
Bisgaard H
Gilliland FD
Heinrich J
Wheeler E
Barroso I
O'Rahilly S
Meirhaeghe A
Sørensen TI
Power C
Palmer LJ
Hinney A
Widen E
Farooqi IS
McCarthy MI
Froguel P
Meyre D
Hebebrand J
Jarvelin MR
Jaddoe VW
Smith GD
Hakonarson H
Grant SF
Pokaż więcej
Corporate Authors:
Early Growth Genetics Consortium
Źródło:
Nature genetics [Nat Genet] 2012 May; Vol. 44 (5), pp. 526-31.
Typ publikacji:
Comparative Study; Journal Article; Meta-Analysis; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Genetic Loci*
Genetic Markers*
Genome-Wide Association Study*
Obesity/*genetics
Polymorphism, Single Nucleotide/*genetics
Adolescent ; Adult ; Body Mass Index ; Case-Control Studies ; Genetic Predisposition to Disease ; Humans ; Young Adult
Czasopismo naukowe
Tytuł:
Common variants at 12q15 and 12q24 are associated with infant head circumference.
Autorzy:
Taal HR; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.; Department of Paediatrics, Erasmus Medical Center, Rotterdam, The Netherlands.; The Generation R Study Group, Erasmus Medical Center, Rotterdam, The Netherlands.
Pourcain BS; MRC Centre for Causal Analyses in Translational Epidemiology, School of Social and Community Medicine, University of Bristol, Bristol, UK.
Thiering E; Institute of Epidemiology I, Helmholtz Zentrum München - German Research Center for Environmental Health, Neuherberg, Germany.
Das S; Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, UK.
Mook-Kanamori DO; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.; Department of Paediatrics, Erasmus Medical Center, Rotterdam, The Netherlands.; The Generation R Study Group, Erasmus Medical Center, Rotterdam, The Netherlands.; Weill Cornell Medical College - Qatar, Doha, Qatar.
Warrington NM; School of Women's and Infants' Health, The University of Western Australia, Perth, Australia.; Samuel Lunenfeld Research Institute, University of Toronto, Toronto, Canada.
Kaakinen M; Institute of Health Sciences, University of Oulu, Finland.; Biocenter Oulu, University of Oulu, Finland.
Kreiner-Møller E; Copenhagen Prospective Studies on Asthma in Childhood, University of Copenhagen, Copenhagen, Denmark.
Bradfield JP; Center for Applied Genomics, Abramson Research Center, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
Freathy RM; Genetics of Complex Traits, Peninsula College of Medicine and Dentistry, University of Exeter, Exeter, UK.
Geller F; Department of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark.
Guxens M; Center for Research in Environmental Epidemiology (CREAL), Barcelona, Catalonia, Spain.; Hospital del Mar Research Institute (IMIM), Barcelona, Catalonia, Spain.; CIBER Epidemiologia y Salud Pública (CIBERESP), Barcelona, Catalonia, Spain.
Cousminer DL; Institute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland.
Kerkhof M; Department of Epidemiology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Timpson NJ; MRC Centre for Causal Analyses in Translational Epidemiology, School of Social and Community Medicine, University of Bristol, Bristol, UK.
Ikram MA; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.; Department of Radiology, Erasmus Medical Center, Rotterdam, The Netherlands.
Beilin LJ; School of Medicine and Pharmacology, The University of Western Australia, Perth, Australia.
Bønnelykke K; Copenhagen Prospective Studies on Asthma in Childhood, University of Copenhagen, Copenhagen, Denmark.
Buxton JL; Department of Genomics of Common Disease, School of Public Health, Imperial College London.
Charoen P; Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, UK.; Department of Tropical Hygiene, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Chawes BLK; Copenhagen Prospective Studies on Asthma in Childhood, University of Copenhagen, Copenhagen, Denmark.
Eriksson J; National Institute for Health and Welfare, Helsinki, Finland.; Department of General Practice and Primary Health Care, University of Helsinki, Helsinki, Finland.; Folkhalsan Research Centre, Biomedicum Helsinki, University of Helsinki, Helsinki, Finland.
Evans DM; MRC Centre for Causal Analyses in Translational Epidemiology, School of Social and Community Medicine, University of Bristol, Bristol, UK.
Hofman A; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.; The Generation R Study Group, Erasmus Medical Center, Rotterdam, The Netherlands.
Kemp JP; MRC Centre for Causal Analyses in Translational Epidemiology, School of Social and Community Medicine, University of Bristol, Bristol, UK.
Kim CE; Center for Applied Genomics, Abramson Research Center, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
Klopp N; Research Unit for Molecular Epidemiology, Helmholtz Zentrum München - German Research Center for Environmental Health, Neuherberg, Germany.; Hannover Unified Biobank, Hannover Medical School, Hannover, Germany.
Lahti J; Institute of Behavioural Sciences, University of Helsinki, Helsinki, Finland.
Lye SJ; Samuel Lunenfeld Research Institute, University of Toronto, Toronto, Canada.
McMahon G; MRC Centre for Causal Analyses in Translational Epidemiology, School of Social and Community Medicine, University of Bristol, Bristol, UK.
Mentch FD; Center for Applied Genomics, Abramson Research Center, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
Müller M; Institute of Medical Informatics, Biometry and Epidemiology, Chair of Epidemiology, Ludwig-Maximilians-Universität, Munich, Germany.; Institute of Genetic Epidemiology, Helmholtz Zentrum München - German Research Center for Environmental Health, Neuherberg, Germany.; Department of Medicine I, University Hospital Grosshadern, Ludwig-Maximilians-Universität, Munich, Germany.
O'Reilly PF; Department of Epidemiology and Biostatistics, Imperial College London, W2 1PG London, UK.
Prokopenko I; Oxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Churchill Hospital, Oxford, UK.; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
Rivadeneira F; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.; Department of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands.
Steegers EAP; Department of Obstetrics & Gynecology, Erasmus Medical Center, Rotterdam, The Netherlands.
Sunyer J; Center for Research in Environmental Epidemiology (CREAL), Barcelona, Catalonia, Spain.; Hospital del Mar Research Institute (IMIM), Barcelona, Catalonia, Spain.; CIBER Epidemiologia y Salud Pública (CIBERESP), Barcelona, Catalonia, Spain.; Pompeu Fabra University (UPF), Barcelona, Catalonia, Spain.
Tiesler C; Institute of Epidemiology I, Helmholtz Zentrum München - German Research Center for Environmental Health, Neuherberg, Germany.; Dr Von Hauner Children's Hospital, Ludwig-Maximilians University Munich, Munich, Germany.
Yaghootkar H; Genetics of Complex Traits, Peninsula College of Medicine and Dentistry, University of Exeter, Exeter, UK.
Breteler MMB; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.
Debette S; Department of Neurology, Boston University School of Medicine, Boston, MA, USA.
Fornage M; Institute of Molecular Medicine, Human Genetics Center and Division of Epidemiology, School of Public Health, University of Texas, Houston Health Sciences Center, Houston, TX, USA.
Gudnason V; Icelandic Heart Association, Kopavogus, Iceland.; University of Iceland, Reykjavik, Iceland.
Launer LJ; Laboratory of Epidemiology, Demography and Biometry, National Institute on Aging, National Institute of Health, Bethesda, MD, USA.
van der Lugt A; Department of Radiology, Erasmus Medical Center, Rotterdam, The Netherlands.
Mosley TH; Department of Medicine (Geriatrics), University of Mississippi Medical Center, Jackson, MS, USA.
Seshadri S; Department of Neurology, Boston University School of Medicine, Boston, MA, USA.
Smith AV; Icelandic Heart Association, Kopavogus, Iceland.; University of Iceland, Reykjavik, Iceland.
Vernooij MW; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.; Department of Radiology, Erasmus Medical Center, Rotterdam, The Netherlands.
Blakemore AI; Department of Genomics of Common Disease, School of Public Health, Imperial College London.
Chiavacci RM; Center for Applied Genomics, Abramson Research Center, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
Feenstra B; Department of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark.
Fernandez-Benet J; European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SD, United Kingdom.
Grant SFA; Center for Applied Genomics, Abramson Research Center, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.; Department of Pediatrics, University of Pennsylvania, Philadelphia PA 19104, USA.
Hartikainen AL; Institute of Clinical Medicine/Obstetrics and Gynecology, University of Oulu, Oulu, Finland.
van der Heijden AJ; Department of Paediatrics, Erasmus Medical Center, Rotterdam, The Netherlands.
Iñiguez C; CIBER Epidemiologia y Salud Pública (CIBERESP), Barcelona, Catalonia, Spain.; Division of Environment and Health, Center for Public Health Research-CSISP, Valencia, Spain.
Lathrop M; Centre National de Génotypage, Evry, France.; Foundation Jean Dausset, CEPH, Paris, France.
McArdle WL; School of Social and Community Medicine, University of Bristol, Bristol, UK.
Mølgaard A; Copenhagen Prospective Studies on Asthma in Childhood, University of Copenhagen, Copenhagen, Denmark.
Newnham JP; School of Women's and Infants' Health, The University of Western Australia, Perth, Australia.
Palmer LJ; Samuel Lunenfeld Research Institute, University of Toronto, Toronto, Canada.; Genetic Epidemiology and Biostatistics Platform, Ontario Institute for Cancer Research, Toronto, Ontario, Canada.
Palotie A; Institute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland.; Department of Medical Genetics, University of Helsinki, Helsinki, Finland.; Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA.; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Pouta A; National Institute for Health and Welfare, Oulu, Finland, Biocenter Oulu, University of Oulu, Finland.
Ring SM; School of Social and Community Medicine, University of Bristol, Bristol, UK.
Sovio U; Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, UK.; London School of Hygiene and Tropical Medicine, London, United Kingdom.
Standl M; Institute of Epidemiology I, Helmholtz Zentrum München - German Research Center for Environmental Health, Neuherberg, Germany.
Uitterlinden AG; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.; Department of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands.
Wichmann HE; Institute of Epidemiology I, Helmholtz Zentrum München - German Research Center for Environmental Health, Neuherberg, Germany.; Institute of Medical Informatics, Biometry and Epidemiology, Chair of Epidemiology, Ludwig-Maximilians-Universität, Munich, Germany.; Department of Medicine I, University Hospital Grosshadern, Ludwig-Maximilians-Universität, Munich, Germany.
Vissing NH; Copenhagen Prospective Studies on Asthma in Childhood, University of Copenhagen, Copenhagen, Denmark.
DeCarli C; Department of Neurology and Center for Neuroscience, University of California at Davis, Sacramento, CA, USA.
van Duijn CM; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.
McCarthy MI; Oxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Churchill Hospital, Oxford, UK.; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.; Oxford NIHR Biomedical Research Centre, Churchill Hospital, Oxford, UK.
Koppelman GH; Department of Pediatric Pulmonology and Pediatric Allergology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Estivill X; CIBER Epidemiologia y Salud Pública (CIBERESP), Barcelona, Catalonia, Spain.; Pompeu Fabra University (UPF), Barcelona, Catalonia, Spain.; Genes and Disease Program, Center for Genomic Regulation (CRG-UPF), Barcelona, Catalonia, Spain.
Hattersley AT; Peninsula NIHR Clinical Research Facility, Peninsula College of Medicine and Dentistry, University of Exeter, Exeter, UK.
Melbye M; Department of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark.
Bisgaard H; Copenhagen Prospective Studies on Asthma in Childhood, University of Copenhagen, Copenhagen, Denmark.
Pennell CE; School of Women's and Infants' Health, The University of Western Australia, Perth, Australia.
Widen E; Institute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland.
Hakonarson H; Center for Applied Genomics, Abramson Research Center, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.; Department of Pediatrics, University of Pennsylvania, Philadelphia PA 19104, USA.
Smith GD; MRC Centre for Causal Analyses in Translational Epidemiology, School of Social and Community Medicine, University of Bristol, Bristol, UK.
Heinrich J; Institute of Epidemiology I, Helmholtz Zentrum München - German Research Center for Environmental Health, Neuherberg, Germany.
Jarvelin MR; Institute of Health Sciences, University of Oulu, Finland.; National Institute for Health and Welfare, Oulu, Finland, Biocenter Oulu, University of Oulu, Finland.; Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, MRC Health Protection Agency (HPA) Centre for Environment and Health, Imperial College London.
Jaddoe VWV; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.; Department of Paediatrics, Erasmus Medical Center, Rotterdam, The Netherlands.; The Generation R Study Group, Erasmus Medical Center, Rotterdam, The Netherlands.
Pokaż więcej
Corporate Authors:
Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium
Early Genetics & Lifecourse Epidemiology (EAGLE) consortium
Early Growth Genetics (EGG) Consortium
Źródło:
Nature genetics [Nat Genet] 2012 Apr 15; Vol. 44 (5), pp. 532-538. Date of Electronic Publication: 2012 Apr 15.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 12/*genetics
Head/*growth & development
Head/*pathology
Polymorphism, Single Nucleotide/*genetics
Pregnancy Complications/*etiology
Pregnancy Complications/*pathology
White People/*genetics
Female ; Genetic Loci ; Genetic Markers ; Genome-Wide Association Study ; Humans ; Infant ; Male ; Meta-Analysis as Topic ; Pregnancy
Czasopismo naukowe
Tytuł:
Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis.
Autorzy:
Paternoster L; Medical Research Council Centre for Causal Analyses in Translational Epidemiology, University of Bristol, Bristol, UK.
Standl M
Chen CM
Ramasamy A
Bønnelykke K
Duijts L
Ferreira MA
Alves AC
Thyssen JP
Albrecht E
Baurecht H
Feenstra B
Sleiman PM
Hysi P
Warrington NM
Curjuric I
Myhre R
Curtin JA
Groen-Blokhuis MM
Kerkhof M
Sääf A
Franke A
Ellinghaus D
Fölster-Holst R
Dermitzakis E
Montgomery SB
Prokisch H
Heim K
Hartikainen AL
Pouta A
Pekkanen J
Blakemore AI
Buxton JL
Kaakinen M
Duffy DL
Madden PA
Heath AC
Montgomery GW
Thompson PJ
Matheson MC
Le Souëf P
St Pourcain B
Smith GD
Henderson J
Kemp JP
Timpson NJ
Deloukas P
Ring SM
Wichmann HE
Müller-Nurasyid M
Novak N
Klopp N
Rodríguez E
McArdle W
Linneberg A
Menné T
Nohr EA
Hofman A
Uitterlinden AG
van Duijn CM
Rivadeneira F
de Jongste JC
van der Valk RJ
Wjst M
Jogi R
Geller F
Boyd HA
Murray JC
Kim C
Mentch F
March M
Mangino M
Spector TD
Bataille V
Pennell CE
Holt PG
Sly P
Tiesler CM
Thiering E
Illig T
Imboden M
Nystad W
Simpson A
Hottenga JJ
Postma D
Koppelman GH
Smit HA
Söderhäll C
Chawes B
Kreiner-Møller E
Bisgaard H
Melén E
Boomsma DI
Custovic A
Jacobsson B
Probst-Hensch NM
Palmer LJ
Glass D
Hakonarson H
Melbye M
Jarvis DL
Jaddoe VW
Gieger C
Strachan DP
Martin NG
Jarvelin MR
Heinrich J
Evans DM
Weidinger S
Pokaż więcej
Corporate Authors:
Australian Asthma Genetics Consortium (AAGC)
Genetics of Overweight Young Adults (GOYA) Consortium
EArly Genetics & Lifecourse Epidemiology (EAGLE) Consortium
Źródło:
Nature genetics [Nat Genet] 2011 Dec 25; Vol. 44 (2), pp. 187-92. Date of Electronic Publication: 2011 Dec 25.
Typ publikacji:
Journal Article; Meta-Analysis
MeSH Terms:
Genetic Loci*
Genome-Wide Association Study*
Dermatitis, Atopic/*genetics
Cell Differentiation/genetics ; Chromosomes, Human, Pair 11/genetics ; Chromosomes, Human, Pair 20/genetics ; Chromosomes, Human, Pair 5 ; Cytokines/genetics ; DNA-Binding Proteins/genetics ; Dermatitis, Atopic/immunology ; Epidermis/immunology ; Female ; Filaggrin Proteins ; Genetic Predisposition to Disease ; Humans ; Intermediate Filament Proteins/genetics ; Kinesins/genetics ; Male ; Polymorphism, Single Nucleotide ; Risk ; Transcription Factors/genetics
Czasopismo naukowe
Tytuł:
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
Autorzy:
Höglinger GU; Department of Neurology, Philipps-Universität, Marburg, Germany.
Melhem NM
Dickson DW
Sleiman PM
Wang LS
Klei L
Rademakers R
de Silva R
Litvan I
Riley DE
van Swieten JC
Heutink P
Wszolek ZK
Uitti RJ
Vandrovcova J
Hurtig HI
Gross RG
Maetzler W
Goldwurm S
Tolosa E
Borroni B
Pastor P
Cantwell LB
Han MR
Dillman A
van der Brug MP
Gibbs JR
Cookson MR
Hernandez DG
Singleton AB
Farrer MJ
Yu CE
Golbe LI
Revesz T
Hardy J
Lees AJ
Devlin B
Hakonarson H
Müller U
Schellenberg GD
Pokaż więcej
Corporate Authors:
PSP Genetics Study Group
Źródło:
Nature genetics [Nat Genet] 2011 Jun 19; Vol. 43 (7), pp. 699-705. Date of Electronic Publication: 2011 Jun 19.
Typ publikacji:
Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
MeSH Terms:
Genetic Loci*
Genetic Predisposition to Disease*
Genetic Variation*
Genome-Wide Association Study*
Supranuclear Palsy, Progressive/*genetics
Tauopathies/*genetics
tau Proteins/*genetics
Case-Control Studies ; Chromosomes, Human/genetics ; Cohort Studies ; Humans ; Polymorphism, Single Nucleotide/genetics ; Prognosis ; Risk Factors ; Supranuclear Palsy, Progressive/pathology ; Tauopathies/pathology
Czasopismo naukowe
Tytuł:
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
Autorzy:
Naj AC; The John P. Hussman Institute for Human Genomics, University of Miami, Miami, Florida, USA.
Jun G
Beecham GW
Wang LS
Vardarajan BN
Buros J
Gallins PJ
Buxbaum JD
Jarvik GP
Crane PK
Larson EB
Bird TD
Boeve BF
Graff-Radford NR
De Jager PL
Evans D
Schneider JA
Carrasquillo MM
Ertekin-Taner N
Younkin SG
Cruchaga C
Kauwe JS
Nowotny P
Kramer P
Hardy J
Huentelman MJ
Myers AJ
Barmada MM
Demirci FY
Baldwin CT
Green RC
Rogaeva E
St George-Hyslop P
Arnold SE
Barber R
Beach T
Bigio EH
Bowen JD
Boxer A
Burke JR
Cairns NJ
Carlson CS
Carney RM
Carroll SL
Chui HC
Clark DG
Corneveaux J
Cotman CW
Cummings JL
DeCarli C
DeKosky ST
Diaz-Arrastia R
Dick M
Dickson DW
Ellis WG
Faber KM
Fallon KB
Farlow MR
Ferris S
Frosch MP
Galasko DR
Ganguli M
Gearing M
Geschwind DH
Ghetti B
Gilbert JR
Gilman S
Giordani B
Glass JD
Growdon JH
Hamilton RL
Harrell LE
Head E
Honig LS
Hulette CM
Hyman BT
Jicha GA
Jin LW
Johnson N
Karlawish J
Karydas A
Kaye JA
Kim R
Koo EH
Kowall NW
Lah JJ
Levey AI
Lieberman AP
Lopez OL
Mack WJ
Marson DC
Martiniuk F
Mash DC
Masliah E
McCormick WC
McCurry SM
McDavid AN
McKee AC
Mesulam M
Miller BL
Miller CA
Miller JW
Parisi JE
Perl DP
Peskind E
Petersen RC
Poon WW
Quinn JF
Rajbhandary RA
Raskind M
Reisberg B
Ringman JM
Roberson ED
Rosenberg RN
Sano M
Schneider LS
Seeley W
Shelanski ML
Slifer MA
Smith CD
Sonnen JA
Spina S
Stern RA
Tanzi RE
Trojanowski JQ
Troncoso JC
Van Deerlin VM
Vinters HV
Vonsattel JP
Weintraub S
Welsh-Bohmer KA
Williamson J
Woltjer RL
Cantwell LB
Dombroski BA
Beekly D
Lunetta KL
Martin ER
Kamboh MI
Saykin AJ
Reiman EM
Bennett DA
Morris JC
Montine TJ
Goate AM
Blacker D
Tsuang DW
Hakonarson H
Kukull WA
Foroud TM
Haines JL
Mayeux R
Pericak-Vance MA
Farrer LA
Schellenberg GD
Pokaż więcej
Źródło:
Nature genetics [Nat Genet] 2011 May; Vol. 43 (5), pp. 436-41. Date of Electronic Publication: 2011 Apr 03.
Typ publikacji:
Journal Article; Meta-Analysis; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Adaptor Proteins, Signal Transducing/*genetics
Alzheimer Disease/*genetics
Antigens, CD/*genetics
Antigens, Differentiation, Myelomonocytic/*genetics
Cytoskeletal Proteins/*genetics
Membrane Proteins/*genetics
Receptor, EphA1/*genetics
Age of Onset ; Aged ; Aged, 80 and over ; Cohort Studies ; Databases, Genetic ; Female ; Genetic Predisposition to Disease ; Genetic Variation ; Genome-Wide Association Study ; Humans ; Male ; Multigene Family ; Polymorphism, Single Nucleotide ; Sialic Acid Binding Ig-like Lectin 3
Czasopismo naukowe
Tytuł:
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.
Autorzy:
Anderson CA; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, UK.
Boucher G
Lees CW
Franke A
D'Amato M
Taylor KD
Lee JC
Goyette P
Imielinski M
Latiano A
Lagacé C
Scott R
Amininejad L
Bumpstead S
Baidoo L
Baldassano RN
Barclay M
Bayless TM
Brand S
Büning C
Colombel JF
Denson LA
De Vos M
Dubinsky M
Edwards C
Ellinghaus D
Fehrmann RS
Floyd JA
Florin T
Franchimont D
Franke L
Georges M
Glas J
Glazer NL
Guthery SL
Haritunians T
Hayward NK
Hugot JP
Jobin G
Laukens D
Lawrance I
Lémann M
Levine A
Libioulle C
Louis E
McGovern DP
Milla M
Montgomery GW
Morley KI
Mowat C
Ng A
Newman W
Ophoff RA
Papi L
Palmieri O
Peyrin-Biroulet L
Panés J
Phillips A
Prescott NJ
Proctor DD
Roberts R
Russell R
Rutgeerts P
Sanderson J
Sans M
Schumm P
Seibold F
Sharma Y
Simms LA
Seielstad M
Steinhart AH
Targan SR
van den Berg LH
Vatn M
Verspaget H
Walters T
Wijmenga C
Wilson DC
Westra HJ
Xavier RJ
Zhao ZZ
Ponsioen CY
Andersen V
Torkvist L
Gazouli M
Anagnou NP
Karlsen TH
Kupcinskas L
Sventoraityte J
Mansfield JC
Kugathasan S
Silverberg MS
Halfvarson J
Rotter JI
Mathew CG
Griffiths AM
Gearry R
Ahmad T
Brant SR
Chamaillard M
Satsangi J
Cho JH
Schreiber S
Daly MJ
Barrett JC
Parkes M
Annese V
Hakonarson H
Radford-Smith G
Duerr RH
Vermeire S
Weersma RK
Rioux JD
Pokaż więcej
Źródło:
Nature genetics [Nat Genet] 2011 Mar; Vol. 43 (3), pp. 246-52. Date of Electronic Publication: 2011 Feb 06.
Typ publikacji:
Journal Article; Meta-Analysis; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Colitis, Ulcerative/*genetics
Crohn Disease/genetics ; Genome-Wide Association Study ; Humans ; Risk
Czasopismo naukowe
Tytuł:
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.
Autorzy:
Franke A; Institute of Clinical Molecular Biology, Christian-Albrechts-University Kiel, Kiel, Germany.
McGovern DP
Barrett JC
Wang K
Radford-Smith GL
Ahmad T
Lees CW
Balschun T
Lee J
Roberts R
Anderson CA
Bis JC
Bumpstead S
Ellinghaus D
Festen EM
Georges M
Green T
Haritunians T
Jostins L
Latiano A
Mathew CG
Montgomery GW
Prescott NJ
Raychaudhuri S
Rotter JI
Schumm P
Sharma Y
Simms LA
Taylor KD
Whiteman D
Wijmenga C
Baldassano RN
Barclay M
Bayless TM
Brand S
Büning C
Cohen A
Colombel JF
Cottone M
Stronati L
Denson T
De Vos M
D'Inca R
Dubinsky M
Edwards C
Florin T
Franchimont D
Gearry R
Glas J
Van Gossum A
Guthery SL
Halfvarson J
Verspaget HW
Hugot JP
Karban A
Laukens D
Lawrance I
Lemann M
Levine A
Libioulle C
Louis E
Mowat C
Newman W
Panés J
Phillips A
Proctor DD
Regueiro M
Russell R
Rutgeerts P
Sanderson J
Sans M
Seibold F
Steinhart AH
Stokkers PC
Torkvist L
Kullak-Ublick G
Wilson D
Walters T
Targan SR
Brant SR
Rioux JD
D'Amato M
Weersma RK
Kugathasan S
Griffiths AM
Mansfield JC
Vermeire S
Duerr RH
Silverberg MS
Satsangi J
Schreiber S
Cho JH
Annese V
Hakonarson H
Daly MJ
Parkes M
Pokaż więcej
Źródło:
Nature genetics [Nat Genet] 2010 Dec; Vol. 42 (12), pp. 1118-25.
Typ publikacji:
Journal Article; Meta-Analysis; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Predisposition to Disease*
Genome-Wide Association Study*
Crohn Disease/*genetics
Genetic Loci/*genetics
Genome, Human/*genetics
Computational Biology ; Crohn Disease/etiology ; Genetic Linkage ; Genetic Variation ; Humans ; Reproducibility of Results
Czasopismo naukowe
Tytuł:
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population.
Autorzy:
Antoniou AC; Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
Wang X
Fredericksen ZS
McGuffog L
Tarrell R
Sinilnikova OM
Healey S
Morrison J
Kartsonaki C
Lesnick T
Ghoussaini M
Barrowdale D
Peock S
Cook M
Oliver C
Frost D
Eccles D
Evans DG
Eeles R
Izatt L
Chu C
Douglas F
Paterson J
Stoppa-Lyonnet D
Houdayer C
Mazoyer S
Giraud S
Lasset C
Remenieras A
Caron O
Hardouin A
Berthet P
Hogervorst FB
Rookus MA
Jager A
van den Ouweland A
Hoogerbrugge N
van der Luijt RB
Meijers-Heijboer H
Gómez García EB
Devilee P
Vreeswijk MP
Lubinski J
Jakubowska A
Gronwald J
Huzarski T
Byrski T
Górski B
Cybulski C
Spurdle AB
Holland H
Goldgar DE
John EM
Hopper JL
Southey M
Buys SS
Daly MB
Terry MB
Schmutzler RK
Wappenschmidt B
Engel C
Meindl A
Preisler-Adams S
Arnold N
Niederacher D
Sutter C
Domchek SM
Nathanson KL
Rebbeck T
Blum JL
Piedmonte M
Rodriguez GC
Wakeley K
Boggess JF
Basil J
Blank SV
Friedman E
Kaufman B
Laitman Y
Milgrom R
Andrulis IL
Glendon G
Ozcelik H
Kirchhoff T
Vijai J
Gaudet MM
Altshuler D
Guiducci C
Loman N
Harbst K
Rantala J
Ehrencrona H
Gerdes AM
Thomassen M
Sunde L
Peterlongo P
Manoukian S
Bonanni B
Viel A
Radice P
Caldes T
de la Hoya M
Singer CF
Fink-Retter A
Greene MH
Mai PL
Loud JT
Guidugli L
Lindor NM
Hansen TV
Nielsen FC
Blanco I
Lazaro C
Garber J
Ramus SJ
Gayther SA
Phelan C
Narod S
Szabo CI
Benitez J
Osorio A
Nevanlinna H
Heikkinen T
Caligo MA
Beattie MS
Hamann U
Godwin AK
Montagna M
Casella C
Neuhausen SL
Karlan BY
Tung N
Toland AE
Weitzel J
Olopade O
Simard J
Soucy P
Rubinstein WS
Arason A
Rennert G
Martin NG
Montgomery GW
Chang-Claude J
Flesch-Janys D
Brauch H
Severi G
Baglietto L
Cox A
Cross SS
Miron P
Gerty SM
Tapper W
Yannoukakos D
Fountzilas G
Fasching PA
Beckmann MW
Dos Santos Silva I
Peto J
Lambrechts D
Paridaens R
Rüdiger T
Försti A
Winqvist R
Pylkäs K
Diasio RB
Lee AM
Eckel-Passow J
Vachon C
Blows F
Driver K
Dunning A
Pharoah PP
Offit K
Pankratz VS
Hakonarson H
Chenevix-Trench G
Easton DF
Couch FJ
Pokaż więcej
Corporate Authors:
EMBRACE
GEMO Study Collaborators
HEBON
kConFab
SWE-BRCA
MOD SQUAD
GENICA
Źródło:
Nature genetics [Nat Genet] 2010 Oct; Vol. 42 (10), pp. 885-92. Date of Electronic Publication: 2010 Sep 19.
Typ publikacji:
Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Predisposition to Disease*
BRCA1 Protein/*genetics
Breast Neoplasms/*genetics
Chromosomes, Human, Pair 19/*genetics
Mutation/*genetics
Receptor, ErbB-2/*genetics
Receptors, Estrogen/*genetics
Receptors, Progesterone/*genetics
Adult ; Breast Neoplasms/pathology ; Case-Control Studies ; Female ; Genotype ; Humans ; Polymorphism, Single Nucleotide/genetics
Czasopismo naukowe
Tytuł:
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight.
Autorzy:
Freathy RM; Genetics of Complex Traits, Peninsula College of Medicine and Dentistry, University of Exeter, Exeter, UK.
Mook-Kanamori DO
Sovio U
Prokopenko I
Timpson NJ
Berry DJ
Warrington NM
Widen E
Hottenga JJ
Kaakinen M
Lange LA
Bradfield JP
Kerkhof M
Marsh JA
Mägi R
Chen CM
Lyon HN
Kirin M
Adair LS
Aulchenko YS
Bennett AJ
Borja JB
Bouatia-Naji N
Charoen P
Coin LJ
Cousminer DL
de Geus EJ
Deloukas P
Elliott P
Evans DM
Froguel P
Glaser B
Groves CJ
Hartikainen AL
Hassanali N
Hirschhorn JN
Hofman A
Holly JM
Hyppönen E
Kanoni S
Knight BA
Laitinen J
Lindgren CM
McArdle WL
O'Reilly PF
Pennell CE
Postma DS
Pouta A
Ramasamy A
Rayner NW
Ring SM
Rivadeneira F
Shields BM
Strachan DP
Surakka I
Taanila A
Tiesler C
Uitterlinden AG
van Duijn CM
Wijga AH
Willemsen G
Zhang H
Zhao J
Wilson JF
Steegers EA
Hattersley AT
Eriksson JG
Peltonen L
Mohlke KL
Grant SF
Hakonarson H
Koppelman GH
Dedoussis GV
Heinrich J
Gillman MW
Palmer LJ
Frayling TM
Boomsma DI
Davey Smith G
Power C
Jaddoe VW
Jarvelin MR
McCarthy MI
Pokaż więcej
Corporate Authors:
Genetic Investigation of ANthropometric Traits (GIANT) Consortium
Meta-Analyses of Glucose and Insulin-related traits Consortium
Wellcome Trust Case Control Consortium
Early Growth Genetics (EGG) Consortium
Źródło:
Nature genetics [Nat Genet] 2010 May; Vol. 42 (5), pp. 430-5. Date of Electronic Publication: 2010 Apr 06.
Typ publikacji:
Journal Article; Meta-Analysis; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Adenylyl Cyclases/*genetics
Cyclins/*genetics
Isoenzymes/*genetics
Alleles ; Birth Weight ; Cohort Studies ; Diabetes Mellitus, Type 2/genetics ; Ethnicity ; Female ; Genetic Predisposition to Disease ; Genotype ; Glucose/metabolism ; Humans ; Male ; Models, Genetic ; Pregnancy
Czasopismo naukowe
Tytuł:
Common variants at 5q22 associate with pediatric eosinophilic esophagitis.
Autorzy:
Rothenberg ME; Division of Allergy and Immunology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, Ohio, USA.
Spergel JM
Sherrill JD
Annaiah K
Martin LJ
Cianferoni A
Gober L
Kim C
Glessner J
Frackelton E
Thomas K
Blanchard C
Liacouras C
Verma R
Aceves S
Collins MH
Brown-Whitehorn T
Putnam PE
Franciosi JP
Chiavacci RM
Grant SF
Abonia JP
Sleiman PM
Hakonarson H
Pokaż więcej
Źródło:
Nature genetics [Nat Genet] 2010 Apr; Vol. 42 (4), pp. 289-91. Date of Electronic Publication: 2010 Mar 07.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 5*
Cytokines/*genetics
Eosinophils/*pathology
Esophagitis/*genetics
Child ; Esophagitis/pathology ; Eye Proteins/genetics ; Genome-Wide Association Study ; Humans ; Polymorphism, Single Nucleotide ; Thymic Stromal Lymphopoietin
Czasopismo naukowe
Tytuł:
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.
Autorzy:
Van Deerlin VM; [1] Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA. [2] These authors contributed equally to this work.
Sleiman PM
Martinez-Lage M
Chen-Plotkin A
Wang LS
Graff-Radford NR
Dickson DW
Rademakers R
Boeve BF
Grossman M
Arnold SE
Mann DM
Pickering-Brown SM
Seelaar H
Heutink P
van Swieten JC
Murrell JR
Ghetti B
Spina S
Grafman J
Hodges J
Spillantini MG
Gilman S
Lieberman AP
Kaye JA
Woltjer RL
Bigio EH
Mesulam M
Al-Sarraj S
Troakes C
Rosenberg RN
White CL 3rd
Ferrer I
Lladó A
Neumann M
Kretzschmar HA
Hulette CM
Welsh-Bohmer KA
Miller BL
Alzualde A
Lopez de Munain A
McKee AC
Gearing M
Levey AI
Lah JJ
Hardy J
Rohrer JD
Lashley T
Mackenzie IR
Feldman HH
Hamilton RL
Dekosky ST
van der Zee J
Kumar-Singh S
Van Broeckhoven C
Mayeux R
Vonsattel JP
Troncoso JC
Kril JJ
Kwok JB
Halliday GM
Bird TD
Ince PG
Shaw PJ
Cairns NJ
Morris JC
McLean CA
DeCarli C
Ellis WG
Freeman SH
Frosch MP
Growdon JH
Perl DP
Sano M
Bennett DA
Schneider JA
Beach TG
Reiman EM
Woodruff BK
Cummings J
Vinters HV
Miller CA
Chui HC
Alafuzoff I
Hartikainen P
Seilhean D
Galasko D
Masliah E
Cotman CW
Tuñón MT
Martínez MC
Munoz DG
Carroll SL
Marson D
Riederer PF
Bogdanovic N
Schellenberg GD
Hakonarson H
Trojanowski JQ
Lee VM
Pokaż więcej
Źródło:
Nature genetics [Nat Genet] 2010 Mar; Vol. 42 (3), pp. 234-9. Date of Electronic Publication: 2010 Feb 14.
Typ publikacji:
Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 7*
Polymorphism, Single Nucleotide*
DNA-Binding Proteins/*metabolism
Frontotemporal Lobar Degeneration/*genetics
Inclusion Bodies/*metabolism
Case-Control Studies ; Frontotemporal Lobar Degeneration/metabolism ; Gene Frequency ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Genotype ; Humans ; Inclusion Bodies/genetics ; Intercellular Signaling Peptides and Proteins/genetics ; Linkage Disequilibrium ; Membrane Proteins/genetics ; Progranulins
Czasopismo naukowe

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