Autor: "Paterson AD" - OpacWWW

Skocz do pozycji: 1.

Tytuł:: Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans.
Autorzy:: Bailey-Wilson JE; Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, Maryland 21224, USA. />Almasy L
de Andrade M
Bailey J
Bickeböller H
Cordell HJ
Daw EW
Goldin L
Goode EL
Gray-McGuire C
Hening W
Jarvik G
Maher BS
Mendell N
Paterson AD
Rice J
Satten G
Suarez B
Vieland V
Wilcox M
Zhang H
Ziegler A
MacCluer JW; Pokaż więcej
Źródło:: BMC genetics [BMC Genet] 2005 Dec 30; Vol. 6 Suppl 1, pp. S1. Date of Electronic Publication: 2005 Dec 30.
Typ publikacji:: Introductory Journal Article
MeSH Terms:: Genome-Wide Association Study*
Genetic Loci/*genetics
Microsatellite Repeats/*genetics
Polymorphism, Single Nucleotide/*genetics
Databases, Genetic ; Genetic Markers ; Humans

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Skocz do pozycji: 2.

Tytuł:: GWAS for the composite traits of hematuria and albuminuria.
Autorzy:: Gagliano Taliun SA; Department of Medicine and Department of Neurosciences, Université de Montréal, Montréal, QC, Canada.; Montréal Heart Institute, Montréal, QC, Canada.
Dinsmore IR; Department of Genomic Health, Geisinger, Danville, PA, USA.
Mirshahi T; Department of Genomic Health, Geisinger, Danville, PA, USA.
Chang AR; Department of Population Health Sciences, Center for Kidney Health Research, Geisinger, Danville, PA, USA.; Department of Nephrology, Geisinger, Danville, PA, USA.
Paterson AD; Divisions of Epidemiology and Biostatistics, Dalla Lana School of Public Health, Toronto, ON, Canada. andrew.paterson@sickkids.ca.; Genetics and Genome Biology, Research Institute at the Hospital for Sick Children, Toronto, ON, Canada. andrew.paterson@sickkids.ca.; Institute of Medical Sciences, University of Toronto, Toronto, ON, Canada. andrew.paterson@sickkids.ca.
Barua M; Institute of Medical Sciences, University of Toronto, Toronto, ON, Canada. .; Division of Nephrology, University Health Network, Toronto, ON, Canada. .; Department of Medicine, University of Toronto, Toronto, ON, Canada. .; Toronto General Hospital Research Institute, 8NU-855, 200 Elizabeth Street, Toronto, ON, M5G2C4, Canada. .; Pokaż więcej
Źródło:: Scientific reports [Sci Rep] 2023 Oct 23; Vol. 13 (1), pp. 18084. Date of Electronic Publication: 2023 Oct 23.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Hematuria*/genetics
Genome-Wide Association Study*
Female ; Humans ; Albuminuria/genetics ; Phenotype ; Genes, MHC Class I ; Polymorphism, Single Nucleotide

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Skocz do pozycji: 3.

Tytuł:: Integrating variant functional annotation scores have varied abilities to improve power of genome-wide association studies.
Autorzy:: Gao J; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, Canada.
Espin-Garcia O; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, Canada.; Department of Biostatistics, Princess Margaret Cancer Centre, University Health Network, Toronto, Canada.
Paterson AD; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, Canada.; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Canada.
Sun L; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, Canada. .; Department of Statistical Sciences, Faculty of Arts and Science, University of Toronto, Toronto, Canada. .; Pokaż więcej
Źródło:: Scientific reports [Sci Rep] 2022 Jun 24; Vol. 12 (1), pp. 10720. Date of Electronic Publication: 2022 Jun 24.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Genome-Wide Association Study*/methods
Polymorphism, Single Nucleotide*
Gene Frequency ; Open Reading Frames ; Phenotype

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Skocz do pozycji: 4.

Tytuł:: DNA methylation age calculators reveal association with diabetic neuropathy in type 1 diabetes.
Autorzy:: Roshandel D; Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, ON, Canada.
Chen Z; Department of Diabetes Complications and Metabolism, Beckman Research Institute of City of Hope, Duarte, CA, USA.
Canty AJ; Department of Mathematics and Statistics, McMaster University, Hamilton, ON, Canada.
Bull SB; Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, ON, Canada.; Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada.
Natarajan R; Department of Diabetes Complications and Metabolism, Beckman Research Institute of City of Hope, Duarte, CA, USA.
Paterson AD; Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, ON, Canada. Andrew.paterson@sickkids.ca.; Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada. Andrew.paterson@sickkids.ca.; Pokaż więcej
Corporate Authors:: DCCT/EDIC Research Group
Źródło:: Clinical epigenetics [Clin Epigenetics] 2020 Apr 05; Vol. 12 (1), pp. 52. Date of Electronic Publication: 2020 Apr 05.
Typ publikacji:: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:: DNA Methylation*
Diabetes Mellitus, Type 1/*complications
Diabetic Neuropathies/*genetics
Genome-Wide Association Study/*methods
Adolescent ; Adult ; Albumins/metabolism ; CpG Islands ; Diabetes Mellitus, Type 1/genetics ; Diabetes Mellitus, Type 1/metabolism ; Diabetic Neuropathies/metabolism ; Epigenesis, Genetic ; Female ; Humans ; Male ; Oligonucleotide Array Sequence Analysis ; Young Adult

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Skocz do pozycji: 5.

Tytuł:: Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes.
Autorzy:: Charmet R; Institut National pour la Santé et la Recherche Médicale (INSERM), Unité Mixte de Recherche en Santé (UMR_S) 1166, Team Genomics & Pathophysiology of Cardiovascular Diseases, Sorbonne Universités, UPMC Univ. Paris 06, Paris, France.; ICAN Institute for Cardiometabolism and Nutrition, Paris, France.
Duffy S; Centre for Public Health, Queen's University of Belfast, Belfast, Northern Ireland, UK.
Keshavarzi S; Genetics & Genome Biology Program, Hospital for Sick Children, Toronto, Canada.
Gyorgy B; Institut National pour la Santé et la Recherche Médicale (INSERM), Unité Mixte de Recherche en Santé (UMR_S) 1166, Team Genomics & Pathophysiology of Cardiovascular Diseases, Sorbonne Universités, UPMC Univ. Paris 06, Paris, France.; ICAN Institute for Cardiometabolism and Nutrition, Paris, France.
Marre M; Départment de Diabétologie, Endocrinologie et Nutrition, Assistance Publique Hôpitaux de Paris, Hôpital Bichat, DHU FIRE, Paris, France.; UFR de Médecine, Université Paris Diderot, Sorbonne Paris Cité, Paris, France.
Rossing P; Steno Diabetes Center Copenhagen, Gentofte, Denmark.; University of Copenhagen, Copenhagen, Denmark.
McKnight AJ; Centre for Public Health, Queen's University of Belfast, Belfast, Northern Ireland, UK.
Maxwell AP; Centre for Public Health, Queen's University of Belfast, Belfast, Northern Ireland, UK.
Ahluwalia TVS; Steno Diabetes Center Copenhagen, Gentofte, Denmark.
Paterson AD; Genetics & Genome Biology Program, Hospital for Sick Children, Toronto, Canada.; Dalla Lana School of Public Health, University of Toronto, Toronto, Canada.
Trégouët DA; Institut National pour la Santé et la Recherche Médicale (INSERM), Unité Mixte de Recherche en Santé (UMR_S) 1166, Team Genomics & Pathophysiology of Cardiovascular Diseases, Sorbonne Universités, UPMC Univ. Paris 06, Paris, France. .; ICAN Institute for Cardiometabolism and Nutrition, Paris, France. .
Hadjadj S; UFR de Médecine et Pharmacie, Université de Poitiers, Poitiers, France. .; INSERM, CIC 1402 & U1082, Poitiers, France. .; Service d'Endocrinologie-Diabétologie and Centre d'Investigation Clinique, CHU de Poitiers, BP 577, 86021, Poitiers Cedex, France. .; Pokaż więcej
Źródło:: Cardiovascular diabetology [Cardiovasc Diabetol] 2018 Apr 25; Vol. 17 (1), pp. 61. Date of Electronic Publication: 2018 Apr 25.
Typ publikacji:: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't
MeSH Terms:: Genetic Loci*
Polymorphism, Single Nucleotide*
Coronary Artery Disease/*genetics
Diabetes Mellitus, Type 1/*genetics
Adaptor Proteins, Signal Transducing/genetics ; Apolipoproteins E/genetics ; Case-Control Studies ; Collagen Type IV/genetics ; Comorbidity ; Coronary Artery Disease/diagnosis ; Coronary Artery Disease/ethnology ; Cyclin-Dependent Kinases/genetics ; Diabetes Mellitus, Type 1/diagnosis ; Diabetes Mellitus, Type 1/ethnology ; Europe/epidemiology ; Genetic Markers ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Humans ; Phenotype ; Risk Factors ; TRPP Cation Channels/genetics ; White People/genetics

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Skocz do pozycji: 6.

Tytuł:: Letter to the editor: expression of concern, reaffirmed.
Autorzy:: Paterson AD; Program in Genetics and Genome Biology, The Hospital for Sick Children, TMDT East Tower, Room 15-707, 101 College Street, Toronto, ON, M5G 1L7, Canada, andrew.paterson@utoronto.ca.; Pokaż więcej
Źródło:: Age (Dordrecht, Netherlands) [Age (Dordr)] 2014 Feb; Vol. 36 (1), pp. 479-82. Date of Electronic Publication: 2013 Aug 24.
Typ publikacji:: Letter; Comment
MeSH Terms:: Genome-Wide Association Study*
Genomics*
Phenotype*
Polymorphism, Single Nucleotide*
Aging/*genetics
Longevity/*genetics
Female ; Humans ; Male ; Pregnancy

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Skocz do pozycji: 7.

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

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Skocz do pozycji: 8.

Tytuł:: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
Autorzy:: Verhoeven VJ; Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands.
Hysi PG
Wojciechowski R
Fan Q
Guggenheim JA
Höhn R
MacGregor S
Hewitt AW
Nag A
Cheng CY
Yonova-Doing E
Zhou X
Ikram MK
Buitendijk GH
McMahon G
Kemp JP
Pourcain BS
Simpson CL
Mäkelä KM
Lehtimäki T
Kähönen M
Paterson AD
Hosseini SM
Wong HS
Xu L
Jonas JB
Pärssinen O
Wedenoja J
Yip SP
Ho DW
Pang CP
Chen LJ
Burdon KP
Craig JE
Klein BE
Klein R
Haller T
Metspalu A
Khor CC
Tai ES
Aung T
Vithana E
Tay WT
Barathi VA
Chen P
Li R
Liao J
Zheng Y
Ong RT
Döring A
Evans DM
Timpson NJ
Verkerk AJ
Meitinger T
Raitakari O
Hawthorne F
Spector TD
Karssen LC
Pirastu M
Murgia F
Ang W
Mishra A
Montgomery GW
Pennell CE
Cumberland PM
Cotlarciuc I
Mitchell P
Wang JJ
Schache M
Janmahasatian S
Igo RP Jr
Lass JH
Chew E
Iyengar SK
Gorgels TG
Rudan I
Hayward C
Wright AF
Polasek O
Vatavuk Z
Wilson JF
Fleck B
Zeller T
Mirshahi A
Müller C
Uitterlinden AG
Rivadeneira F
Vingerling JR
Hofman A
Oostra BA
Amin N
Bergen AA
Teo YY
Rahi JS
Vitart V
Williams C
Baird PN
Wong TY
Oexle K
Pfeiffer N
Mackey DA
Young TL
van Duijn CM
Saw SM
Bailey-Wilson JE
Stambolian D
Klaver CC
Hammond CJ; Pokaż więcej
Corporate Authors:: Consortium for Refractive Error and Myopia (CREAM)
Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group
Wellcome Trust Case Control Consortium 2 (WTCCC2)
Fuchs' Genetics Multi-Center Study Group
Źródło:: Nature genetics [Nat Genet] 2013 Mar; Vol. 45 (3), pp. 314-8. Date of Electronic Publication: 2013 Feb 10.
Typ publikacji:: Journal Article; Meta-Analysis; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
MeSH Terms:: Genome-Wide Association Study*
Myopia/*genetics
Refractive Errors/*genetics
Alcohol Oxidoreductases/genetics ; Asian People/genetics ; Bone Morphogenetic Protein 2/genetics ; Genetic Predisposition to Disease ; Homeodomain Proteins/genetics ; Humans ; KCNQ Potassium Channels/genetics ; Laminin/genetics ; Receptors, AMPA/genetics ; Risk Factors ; Serine Proteases/genetics ; Trans-Activators/genetics ; White People/genetics

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Skocz do pozycji: 9.

Tytuł:: Common genetic determinants of intraocular pressure and primary open-angle glaucoma.
Autorzy:: van Koolwijk LM; Glaucoma Service, The Rotterdam Eye Hospital, Rotterdam, The Netherlands.
Ramdas WD
Ikram MK
Jansonius NM
Pasutto F
Hysi PG
Macgregor S
Janssen SF
Hewitt AW
Viswanathan AC
ten Brink JB
Hosseini SM
Amin N
Despriet DD
Willemse-Assink JJ
Kramer R
Rivadeneira F
Struchalin M
Aulchenko YS
Weisschuh N
Zenkel M
Mardin CY
Gramer E
Welge-Lüssen U
Montgomery GW
Carbonaro F
Young TL
Bellenguez C
McGuffin P
Foster PJ
Topouzis F
Mitchell P
Wang JJ
Wong TY
Czudowska MA
Hofman A
Uitterlinden AG
Wolfs RC
de Jong PT
Oostra BA
Paterson AD
Mackey DA
Bergen AA
Reis A
Hammond CJ
Vingerling JR
Lemij HG
Klaver CC
van Duijn CM; Pokaż więcej
Corporate Authors:: DCCT/EDIC Research Group
Wellcome Trust Case Control Consortium 2
Źródło:: PLoS genetics [PLoS Genet] 2012; Vol. 8 (5), pp. e1002611. Date of Electronic Publication: 2012 May 03.
Typ publikacji:: Journal Article; Meta-Analysis; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:: Genome-Wide Association Study*
Glaucoma, Open-Angle/*genetics
Intraocular Pressure/*genetics
Nerve Tissue Proteins/*genetics
Aged ; Aged, 80 and over ; Case-Control Studies ; Ciliary Body/metabolism ; Ciliary Body/pathology ; Female ; Humans ; Male ; Middle Aged ; Optic Nerve/metabolism ; Optic Nerve/pathology ; Polymorphism, Single Nucleotide ; Trabecular Meshwork/metabolism ; Trabecular Meshwork/pathology

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Skocz do pozycji: 10.

Tytuł:: Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.
Autorzy:: Nolte IM; Unit of Genetic Epidemiology and Bioinformatics, Department of Epidemiology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Wallace C
Newhouse SJ
Waggott D
Fu J
Soranzo N
Gwilliam R
Deloukas P
Savelieva I
Zheng D
Dalageorgou C
Farrall M
Samani NJ
Connell J
Brown M
Dominiczak A
Lathrop M
Zeggini E
Wain LV
Newton-Cheh C
Eijgelsheim M
Rice K
de Bakker PI
Pfeufer A
Sanna S
Arking DE
Asselbergs FW
Spector TD
Carter ND
Jeffery S
Tobin M
Caulfield M
Snieder H
Paterson AD
Munroe PB
Jamshidi Y; Pokaż więcej
Corporate Authors:: Wellcome Trust Case Control Consortium
DCCT/EDIC Research Group
QTGEN consortium
QTSCD consortium
Źródło:: PloS one [PLoS One] 2009 Jul 09; Vol. 4 (7), pp. e6138. Date of Electronic Publication: 2009 Jul 09.
Typ publikacji:: Journal Article; Meta-Analysis; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:: Genetic Variation*
Genome-Wide Association Study*
Calcium-Binding Proteins/*genetics
Heart/*physiology
Chromosomes, Human, Pair 6 ; Cohort Studies ; Humans

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Skocz do pozycji: 11.

Tytuł:: Evaluating outlier loci and their effect on the identification of pedigree errors.
Autorzy:: Wang KS; Program in Genetics and Genomic Biology, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada. />Liu M
Paterson AD; Pokaż więcej
Źródło:: BMC genetics [BMC Genet] 2005 Dec 30; Vol. 6 Suppl 1, pp. S155. Date of Electronic Publication: 2005 Dec 30.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Pedigree*
Genetic Loci/*genetics
Alcoholism/genetics ; Cooperative Behavior ; Databases, Genetic ; Female ; Gene Frequency/genetics ; Genotype ; Humans ; Male ; Research Design

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Skocz do pozycji: 12.

Tytuł:: A genome scan for parent-of-origin linkage effects in alcoholism.
Autorzy:: Liu XQ; Program in Genetics and Genomic Biology, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada. />Greenwood CM
Wang KS
Paterson AD; Pokaż więcej
Źródło:: BMC genetics [BMC Genet] 2005 Dec 30; Vol. 6 Suppl 1, pp. S160. Date of Electronic Publication: 2005 Dec 30.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Genetic Linkage*
Genome-Wide Association Study*
Parents*
Alcoholism/*genetics
Chromosomes, Human, Pair 12/genetics ; Female ; Humans ; Male ; Sex Characteristics

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