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Co-authors
(303)
Tina M. Cowan
9
Seymour Packman
8
Mahin Golabi
8
Victoria A. Cox
7
Kara Weisiger
5
Journals
(27)
MOL GENET METAB
13
AMER J MED GENET
9
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J INHERIT METAB DIS
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Authors
Gregory M. Enns
Gregory M. Enns,Stanford University,Genetics & Genealogy,Molecular Biology,Biochemistry
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Gregory M. Enns
Stanford University
Publications:
70
|
Citations:
513
Fields:
Genetics & Genealogy
,
Molecular Biology
,
Biochemistry
View FAQ about top research areas and Fields of study
Collaborated with
303 co-authors
from 1998 to 2012
|
Cited by
2120 authors
Cumulative
Annual
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Publications
(70)
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Mutations in KAT6B, encoding a histone acetyltransferase, cause Genitopatellar syndrome
P. M. Campeau
,
J. C. Kim
,
J. T. Lu
,
J. A. Schwartzentruber
,
O. A. Abdul-Rahman
,
S. Schlaubitz
,
D. M. Murdock
,
M. M. Jiang
,
E. J. Lammer
,
G. M. Enns
,
W. J. Rhead
,
J. Rowland
http://academic.research.microsoft.com/io.ashx?type=5&id=61415457&selfId1=23876607&selfId2=0&maxNumber=12&query=
Published in 2012.
High-quality DNA sequence capture of 524 disease candidate genes
(
Citations: 1
)
P. Shen
,
W. Wang
,
S. Krishnakumar
,
C. Palm
,
A.-K. Chi
,
G. M. Enns
,
R. W. Davis
,
T. P. Speed
,
M. N. Mindrinos
,
C. Scharfe
Journal:
Proceedings of The National Academy of Sciences - PNAS
, vol. 108, pp. 6549-6554, 2011
α-Tocotrienol quinone modulates oxidative stress response and the biochemistry of aging
(
Citations: 1
)
William D. Shrader
,
Akiko Amagata
,
Adam Barnes
,
Gregory M. Enns
,
Andrew Hinman
,
Orion Jankowski
,
Viktoria Kheifets
,
Ryo Komatsuzaki
,
Edgar Lee
,
Paul Mollard
,
Katsuyuki Murase
,
Alfredo A. Sadun
http://academic.research.microsoft.com/io.ashx?type=5&id=49476498&selfId1=23876607&selfId2=0&maxNumber=12&query=
Journal:
Bioorganic & Medicinal Chemistry Letters - BIOORG MEDICINAL CHEM LETTER
, vol. 21, no. 12, pp. 3693-3698, 2011
A Novel Mutation in the HSD17B10 Gene of a 10YearOld Boy with Refractory Epilepsy, Choreoathetosis and Learning Disability
Laurie H. Seaver
,
Xue-Ying He
,
Keith Abe
,
Tina Cowan
,
Gregory M. Enns
,
Lawrence Sweetman
,
Manfred Philipp
,
Sansan Lee
,
Mazhar Malik
,
Song-Yu Yang
Journal:
PLOS One
, vol. 6, no. 11, 2011
Terminal 22q Deletion Syndrome: A Newly Recognized Cause of Speech and Language Disability in the Autism Spectrum
(
Citations: 23
)
Melanie A. Manning
,
Suzanne B. Cassidy
,
Carol Clericuzio
,
Athena M. Cherry
,
Stuart Schwartz
,
Louanne Hudgins
,
Gregory M. Enns
,
H. Eugene Hoyme
Published in 2010.
Sort by:
Citations
(513 times by 455 publications)
Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis
(
Citations: 2
)
D A Rossignol
,
R E Frye
Journal:
Molecular Psychiatry - MOL PSYCHIATR
, vol. 17, no. 3, pp. 290-314, 2012
Liver Production of Sulfamidase Reverses Peripheral and Ameliorates CNS Pathology in Mucopolysaccharidosis IIIA Mice
Albert Ruzo
,
Miquel Garcia
,
Albert Ribera
,
Pilar Villacampa
,
Virginia Haurigot
,
Sara Marcó
,
Eduard Ayuso
,
Xavier M Anguela
,
Carles Roca
,
Judith Agudo
,
David Ramos
,
Jesús Ruberte
http://academic.research.microsoft.com/io.ashx?type=5&id=56566460&selfId1=23876607&selfId2=0&maxNumber=12&query=
Journal:
Molecular Therapy - MOL THER
, vol. 20, no. 2, pp. 254-266, 2012
Use of selective serotonin reuptake inhibitors during pregnancy and disorganised infant–mother attachment
Beth R. Troutman
,
Allison M. Momany
Journal:
Journal of Reproductive and Infant Psychology - J REPROD INFANT PSYCHOL
, vol. ahead-of-p, no. ahead-of-p, pp. 1-17, 2012
Biomarkers for mitochondrial respiratory chain disorders
(
Citations: 2
)
Anu Suomalainen
Journal:
Journal of Inherited Metabolic Disease - J INHERIT METAB DIS
, vol. 34, no. 2, pp. 277-282, 2011
Mild hyperphenylalaninemia: to treat or not to treat
(
Citations: 2
)
Francjan J. van Spronsen
Journal:
Journal of Inherited Metabolic Disease - J INHERIT METAB DIS
, vol. 34, no. 3, pp. 651-656, 2011
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