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Co-authors
(1125)
Barry Merriman
31
Paul S. Mischel
28
Timothy F. Cloughesy
26
Zugen Chen
25
Susan L. Smalley
24
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Academic
Authors
Stanley F. Nelson
Stanley F. Nelson,University of California Los Angeles,Genetics & Genealogy,Molecular Biology,Neuroscience
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Stanley F. Nelson
University of California Los Angeles
Publications:
196
|
Citations:
5095
Fields:
Genetics & Genealogy
,
Molecular Biology
,
Neuroscience
View FAQ about top research areas and Fields of study
Collaborated with
1125 co-authors
from 1989 to 2012
|
Cited by
18018 authors
Cumulative
Annual
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Publications
(196)
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CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium
Ji Eun Lee
,
Jennifer L Silhavy
,
Maha S Zaki
,
Jana Schroth
,
Stephanie L Bielas
,
Sarah E Marsh
,
Jesus Olvera
,
Francesco Brancati
,
Miriam Iannicelli
,
Koji Ikegami
,
Andrew M Schlossman
,
Barry Merriman
Stanley F Nelson
http://academic.research.microsoft.com/io.ashx?type=5&id=56593584&selfId1=2896292&selfId2=0&maxNumber=12&query=
Journal:
Nature Genetics - NAT GENET
, vol. 44, no. 2, pp. 193-199, 2012
Melanoma whole-exome sequencing identifies V600EB-RAF amplification-mediated acquired B-RAF inhibitor resistance
Hubing Shi
,
Gatien Moriceau
,
Xiangju Kong
,
Mi-Kyung Lee
,
Hane Lee
,
Richard C. Koya
,
Charles Ng
,
Thinle Chodon
,
Richard A. Scolyer
,
Kimberly B. Dahlman
,
Jeffrey A. Sosman
,
Richard F. Kefford
Stanley F. Nelson
http://academic.research.microsoft.com/io.ashx?type=5&id=56583709&selfId1=2896292&selfId2=0&maxNumber=12&query=
Journal:
Nature Communications
, vol. 3, 2012
Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders
Richard J L Anney
,
Elaine M Kenny
,
Colm O'Dushlaine
,
Brian L Yaspan
,
Elena Parkhomenka
,
Joseph D Buxbaum
,
James Sutcliffe
,
Michael Gill
,
Louise Gallagher
,
Bridget A Fernandez
,
Christian R Marshall
,
Dalila Pinto
Stanley F Nelson
http://academic.research.microsoft.com/io.ashx?type=5&id=56548575&selfId1=2896292&selfId2=0&maxNumber=12&query=
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 19, no. 10, pp. 1082-1089, 2011
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder
Josephine Elia
,
Joseph T Glessner
,
Kai Wang
,
Nagahide Takahashi
,
Corina J Shtir
,
Dexter Hadley
,
Patrick M A Sleiman
,
Haitao Zhang
,
Cecilia E Kim
,
Reid Robison
,
Gholson J Lyon
,
James H Flory
Stanley F Nelson
http://academic.research.microsoft.com/io.ashx?type=5&id=56593523&selfId1=2896292&selfId2=0&maxNumber=12&query=
Journal:
Nature Genetics - NAT GENET
, vol. 44, no. 1, pp. 78-84, 2011
Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1
David R Goudie
,
Mariella D'Alessandro
,
Barry Merriman
,
Hane Lee
,
Ildikó Szeverényi
,
Stuart Avery
,
Brian D O'Connor
,
Stanley F Nelson
,
Stephanie E Coats
,
Arlene Stewart
,
Lesley Christie
,
Gabriella Pichert
http://academic.research.microsoft.com/io.ashx?type=5&id=56593700&selfId1=2896292&selfId2=0&maxNumber=12&query=
Journal:
Nature Genetics - NAT GENET
, vol. 43, no. 4, pp. 365-369, 2011
Sort by:
Citations
(5095 times by 4125 publications)
Rare structural variation of synapse and neurotransmission genes in autism
(
Citations: 2
)
X Gai
,
H M Xie
,
J C Perin
,
N Takahashi
,
K Murphy
,
A S Wenocur
,
M D'arcy
,
R J O'Hara
,
E Goldmuntz
,
D E Grice
,
T H Shaikh
,
H Hakonarson
http://academic.research.microsoft.com/io.ashx?type=5&id=56564746&selfId1=2896292&selfId2=0&maxNumber=12&query=
Journal:
Molecular Psychiatry - MOL PSYCHIATR
, vol. 17, no. 4, pp. 402-411, 2012
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=2896292&selfId2=0&maxNumber=12&query=
Journal:
PLOS Genetics - PLOS GENET
, vol. 8, no. 2, 2012
Overexpression of miR370 and downregulation of its novel target TGFβ-RII contribute to the progression of gastric carcinoma
(
Citations: 1
)
S-S Lo
,
P-S Hung
,
J-H Chen
,
H-F Tu
,
W-L Fang
,
C-Y Chen
,
W-T Chen
,
N-R Gong
,
C-W Wu
Journal:
Oncogene
, vol. 31, no. 2, pp. 226-237, 2012
SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism
(
Citations: 1
)
C M Durand
,
J Perroy
,
F Loll
,
D Perrais
,
L Fagni
,
T Bourgeron
,
M Montcouquiol
,
N Sans
Journal:
Molecular Psychiatry - MOL PSYCHIATR
, vol. 17, no. 1, pp. 71-84, 2012
De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
G Kirov
,
A J Pocklington
,
P Holmans
,
D Ivanov
,
M Ikeda
,
D Ruderfer
,
J Moran
,
K Chambert
,
D Toncheva
,
L Georgieva
,
D Grozeva
,
M Fjodorova
http://academic.research.microsoft.com/io.ashx?type=5&id=56564762&selfId1=2896292&selfId2=0&maxNumber=12&query=
Journal:
Molecular Psychiatry - MOL PSYCHIATR
, vol. 17, no. 2, pp. 142-153, 2012
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