Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Przeglądasz jako GOŚĆ

Wyszukujesz frazę ""Ledbetter DH"" wg kryterium: Autor


Tytuł :
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia
Autorzy :
Anney, RJL
Ripke, S
Anttila, V
Grove, J
Holmans, P
Huang, H
Klei, L
Lee, PH
Medland, SE
Neale, B
Robinson, E
Weiss, LA
Zwaigenbaum, L
Yu, TW
Wittemeyer, K
Willsey, AJ
Wijsman, EM
Werge, T
Wassink, TH
Waltes, R
Walsh, CA
Wallace, S
Vorstman, JAS
Vieland, VJ
Vicente, AM
vanEngeland, H
Tsang, K
Thompson, AP
Szatmari, P
Svantesson, O
Steinberg, S
Stefansson, K
Stefansson, H
State, MW
Soorya, L
Silagadze, T
Scherer, SW
Schellenberg, GD
Sandin, S
Sanders, SJ
Saemundsen, E
Rouleau, GA
Roge, B
Roeder, K
Roberts, W
Reichert, J
Reichenberg, A
Rehnstrom, K
Regan, R
Poustka, F
Poultney, CS
Piven, J
Pinto, D
Pericak-Vance, MA
Pejovic-Milovancevic, M
Pedersen, MG
Pedersen, CB
Paterson, AD
Parr, JR
Pagnamenta, AT
Oliveira, G
Nurnberger, JI
Nordentoft, M
Murtha, MT
Mouga, S
Mortensen, PB
Mors, O
Morrow, EM
Moreno-De-Luca, D
Monaco, AP
Minshew, N
Merikangas, A
McMahon, WM
McGrew, SG
Mattheisen, M
Martsenkovsky, I
Martin, DM
Mane, SM
Magnusson, P
Magalhaes, T
Maestrini, E
Lowe, JK
Lord, C
Levitt, P
LeseMartin, C
Ledbetter, DH
Leboyer, M
LeCouteur, AS
Ladd-Acosta, C
Kolevzon, A
Klauck, SM
Jacob, S
Iliadou, B
Hultman, CM
Hougaard, DM
Hertz-Picciotto, I
Hendren, R
Hansen, CS
Haines, JL
Guter, SJ
Grice, DE
Green, JM
Green, A
Goldberg, AP
Gillberg, C
Gilbert, J
Gallagher, L
Freitag, CM
Fombonne, E
Folstein, SE
Fernandez, B
Fallin, MD
Ercan-Sencicek, AG
Ennis, S
Duque, F
Duketis, E
Delorme, R
DeRubeis, S
DeJonge, MV
Dawson, G
Cuccaro, ML
Correia, CT
Conroy, J
Conceicao, IC
Chiocchetti, AG
Celestino-Soper, PBS
Casey, J
Cantor, RM
Cafe, C
Bybjerg-Grauholm, J
Brennan, S
Bourgeron, T
Bolton, PF
Boelte, S
Bolshakova, N
Betancur, C
Bernier, R
Beaudet, AL
Battaglia, A
Bal, VH
Baird, G
Bailey, AJ
Baekvad-Hansen, M
Bader, JS
Bacchelli, E
Anagnostou, E
Amaral, D
Almeida, J
Borglum, AD
Buxbaum, JD
Chakravarti, A
Cook, EH
Coon, H
Geschwind, DH
Gill, M
Hakonarson, H
Hallmayer, J
Palotie, A
Santangelo, S
Sutcliffe, JS
Arking, DE
Devlin, B
Daly, MJ
Pokaż więcej
Temat :
mental disorders
Źródło :
Molecular Autism. 8
Tytuł :
A genome-wide association study of autism using the Simons simplex collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?
Autorzy :
Chaste, P
Klei, L
Sanders, SJ
Hus, V
Murtha, MT
Lowe, JK
Willsey, AJ
Moreno-De-Luca, D
Yu, TW
Fombonne, E
Geschwind, D
Grice, DE
Ledbetter, DH
Mane, SM
Martin, DM
Morrow, EM
Walsh, CA
Sutcliffe, JS
Lese Martin, C
Beaudet, AL
Lord, C
State, MW
Cook, EH
Devlin, B
Pokaż więcej
Temat :
Psychiatry
Biological Sciences
Psychology and Cognitive Sciences
Medical and Health Sciences
Źródło :
Biological Psychiatry, vol 77, iss 9
Opis pliku :
application/pdf
Tytuł :
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
Autorzy :
O'Dushlaine, C
Rossin, L
Lee, Ph
Duncan, L
Parikshak, Nn
Newhouse, S
Ripke, S
Neale, Bm
Purcell, Sm
Posthuma, D
Nurnberger, Ji
Lee, Sh
Faraone, Sv
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
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
Mattheisen, M
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
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
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
Längström, N
Lathrop, M
Lawrence, J
Lawson, Wb
Leboyer, M
Ledbetter, Dh
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
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
Meyer, J
Middeldorp, Cm
Middleton, L
Milanova, V
Miranda, A
Monaco, A
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
Nwulia, Ea
Nyholt, Dr
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
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
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, Jc
Van Grootheest, G
Van Os, J
Vicente, A
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
Kendler, Ks
Weiss, La
Wray, Nr
Zhao, Z
Geschwind, Dh
Sullivan, Pf
Smoller, Jw
Holmans, Pa
Breen, G.
Pokaż więcej
Temat :
Brain
Databases, Genetic
Genetic Predisposition to Disease
Genome-Wide Association Study
Histones
Humans
Mental Disorders
Signal Transduction
Neuroscience (all)
Opis pliku :
STAMPA
Tytuł :
Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts
Autorzy :
State, Matthew
Sanders, Stephan
Moreno-De-Luca, D
Sanders, SJ
Willsey, AJ
Mulle, JG
Lowe, JK
Geschwind, DH
State, MW
Martin, CL
Ledbetter, DH
Pokaż więcej
Temat :
genetic structures
behavioral disciplines and activities
mental disorders
Źródło :
State, Matthew; Sanders, Stephan; Moreno-De-Luca, D; Sanders, SJ; Willsey, AJ; Mulle, JG; et al.(2013). Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/7036973c
Opis pliku :
application/pdf
Tytuł :
Towards an evidence-based process for the clinical interpretation of copy number variation.
Autorzy :
Riggs, ER
Church, DM
Hanson, K
Horner, VL
Kaminsky, EB
Kuhn, RM
Wain, KE
Williams, ES
Aradhya, S
Kearney, HM
Ledbetter, DH
South, ST
Thorland, EC
Martin, CL
Pokaż więcej
Temat :
EVIDENCE-based medicine
MEDICAL decision making
GENETIC testing
MICROARRAY technology
GENOMES
PHENOTYPES
MEDICAL genetics
Źródło :
Clinical Genetics; May2012, Vol. 81 Issue 5, p403-412, 10p, 2 Diagrams
Czasopismo naukowe

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies