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Co-authors
(1189)
Christopher A. Walsh
20
Renzo Guerrini
19
David H. Ledbetter
18
A. James Barkovich
14
Susan L. Christian
14
Journals
(57)
AMER J MED GENET
33
AM J MED GENET PART A
16
ANN NEUROL
15
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NAT GENET
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Authors
William B. Dobyns
William B. Dobyns,University of Washington,Genetics & Genealogy,Neuroscience,Molecular Biology
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William B. Dobyns
University of Washington
Publications:
224
|
Citations:
7392
Fields:
Genetics & Genealogy
,
Neuroscience
,
Molecular Biology
View FAQ about top research areas and Fields of study
Collaborated with
1189 co-authors
from 1979 to 2011
|
Cited by
17497 authors
Cumulative
Annual
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Publications
(224)
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Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function
Alex R Paciorkowski
,
Liu Lin Thio
,
Jill A Rosenfeld
,
Marzena Gajecka
,
Christina A Gurnett
,
Shashikant Kulkarni
,
Wendy K Chung
,
Eric D Marsh
,
Mattia Gentile
,
James D Reggin
,
James W Wheless
,
Sandhya Balasubramanian
William B Dobyns
http://academic.research.microsoft.com/io.ashx?type=5&id=56548405&selfId1=3016754&selfId2=0&maxNumber=12&query=
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 19, no. 12, pp. 1238-1245, 2011
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
Fanny Kortüm
,
Soma Das
,
Max Flindt
,
Deborah J Morris-Rosendahl
,
Irina Stefanova
,
Amy Goldstein
,
Denise Horn
,
Eva Klopocki
,
Gerhard Kluger
,
Peter Martin
,
Anita Rauch
,
Agathe Roumer
William B Dobyns
http://academic.research.microsoft.com/io.ashx?type=5&id=59318650&selfId1=3016754&selfId2=0&maxNumber=12&query=
Journal:
Journal of Medical Genetics - J MED GENET
, vol. 48, no. 6, pp. 396-406, 2011
Bioinformatics and Data-Intensive Scientific Discovery in the Beginning of the 21st Century
Roger Barga
,
Bill Howe
,
David Beck
,
Stuart Bowers
,
William Dobyns
,
Winston Haynes
,
Roger Higdon
,
Chris Howard
,
Christian Roth
,
Elizabeth Stewart
,
Dean Welch
,
Eugene Kolker
Published in 2011.
COL4A1 Mutations Cause Ocular Dysgenesis, Neuronal Localization Defects, and Myopathy in Mice and Walker-Warburg Syndrome in Humans
Cassandre Labelle-Dumais
,
David J. Dilworth
,
Emily P. Harrington
,
Michelle de Leau
,
David Lyons
,
Zhyldyz Kabaeva
,
M. Chiara Manzini
,
William B. Dobyns
,
Christopher A. Walsh
,
Daniel E. Michele
,
Douglas B. Gould
Journal:
PLOS Genetics - PLOS GENET
, vol. 7, no. 5, 2011
SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
(
Citations: 16
)
Vincent Cantagrel
,
Dirk J. Lefeber
,
Bobby G. Ng
,
Ziqiang Guan
,
Jennifer L. Silhavy
,
Stephanie L. Bielas
,
Ludwig Lehle
,
Hans Hombauer
,
Maciej Adamowicz
,
Ewa Swiezewska
,
Arjan P. De Brouwer
,
Peter Blümel
William B. Dobyns
http://academic.research.microsoft.com/io.ashx?type=5&id=36139611&selfId1=3016754&selfId2=0&maxNumber=12&query=
Journal:
Cell
, vol. 142, no. 2, pp. 203-217, 2010
Sort by:
Citations
(7392 times by 4351 publications)
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
Claire S. Leblond
,
Jutta Heinrich
,
Richard Delorme
,
Christian Proepper
,
Catalina Betancur
,
Guillaume Huguet
,
Marina Konyukh
,
Pauline Chaste
,
Elodie Ey
,
Maria Rastam
,
Henrik Anckarsäter
,
Gudrun Nygren
http://academic.research.microsoft.com/io.ashx?type=5&id=57409742&selfId1=3016754&selfId2=0&maxNumber=12&query=
Journal:
PLOS Genetics - PLOS GENET
, vol. 8, no. 2, 2012
Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies
Alistair T Pagnamenta
,
Stefano Lise
,
Victoria Harrison
,
Helen Stewart
,
Sandeep Jayawant
,
Gerardine Quaghebeur
,
Alexander T Deng
,
Valerie Elizabeth Murphy
,
Elham Sadighi Akha
,
Andy Rimmer
,
Iain Mathieson
,
Samantha JL Knight
http://academic.research.microsoft.com/io.ashx?type=5&id=56556970&selfId1=3016754&selfId2=0&maxNumber=12&query=
Journal:
Journal of Human Genetics - J HUM GENET
, vol. 57, no. 1, pp. 70-72, 2012
Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43–q44
Sandesh C Sreenath Nagamani
,
Ayelet Erez
,
Carolyn Bay
,
Anjana Pettigrew
,
Seema R Lalani
,
Kristin Herman
,
Brett H Graham
,
Malgorzata JM Nowaczyk
,
Monica Proud
,
William J Craigen
,
Bobbi Hopkins
,
Beth Kozel
http://academic.research.microsoft.com/io.ashx?type=5&id=56548460&selfId1=3016754&selfId2=0&maxNumber=12&query=
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 20, no. 2, pp. 176-179, 2012
Neurodevelopmental and neuropsychiatric behaviour defects arise from 14-3-3ζ deficiency
P-S Cheah
,
H S Ramshaw
,
P Q Thomas
,
K Toyo-oka
,
X Xu
,
S Martin
,
P Coyle
,
M A Guthridge
,
F Stomski
,
M van den Buuse
,
A Wynshaw-Boris
,
A F Lopez
http://academic.research.microsoft.com/io.ashx?type=5&id=56564764&selfId1=3016754&selfId2=0&maxNumber=12&query=
Journal:
Molecular Psychiatry - MOL PSYCHIATR
, vol. 17, no. 4, pp. 451-466, 2012
RP58/ZNF238 directly modulates proneurogenic gene levels and is required for neuronal differentiation and brain expansion
C Xiang
,
V Baubet
,
S Pal
,
L Holderbaum
,
V Tatard
,
P Jiang
,
R V Davuluri
,
N Dahmane
Journal:
Cell Death and Differentiation - CELL DEATH DIFFERENTIATION
, vol. 19, no. 4, pp. 692-702, 2012
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