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European Journal of Human Genetics : EJHG
|
February 28, 2013
Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHL
Nelly Abdelfatah, David A McComiskey, Lance Doucette, et al.
Journal of the American College of Cardiology
|
February 1, 2005
The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5)
Kathy A Hodgkinson, Patrick S Parfrey, Anne S Bassett, et al.
American Journal of Medical Genetics. Part A
|
March 26, 2018
Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome
Lisa D Palmer, Nancy J Butcher, Erik Boot, et al.
BMC Pregnancy and Childbirth
|
December 21, 2017
Blood pressure self-monitoring in pregnancy (BuMP) feasibility study; a qualitative analysis of women's experiences of self-monitoring
Lisa Hinton, Katherine L Tucker, Sheila M Greenfield, et al.
Biological Psychology
|
December 15, 2007
DISC1 is associated with prefrontal cortical gray matter and positive symptoms in schizophrenia
Philip R Szeszko, Colin A Hodgkinson, Delbert G Robinson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
April 19, 2017
New Repeat Polymorphism in the <i>AKT1</i> Gene Predicts Striatal Dopamine D2/D3 Receptor Availability and Stimulant-Induced Dopamine Release in the Healthy Human Brain
Elena Shumay, Corinde E Wiers, Ehsan Shokri-Kojori, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
March 8, 2014
FKBP5 moderates alcohol withdrawal severity: human genetic association and functional validation in knockout mice
Ming-Chyi Huang, Melanie L Schwandt, Julia A Chester, et al.
Molecular Psychiatry
|
November 11, 2021
Strong and weak cross-inheritance of substance use disorders in a nationally representative sample
Haitao Zhang, Bridget F Grant, Colin A Hodgkinson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 28, 2010
Genome-wide association identifies candidate genes that influence the human electroencephalogram
Colin A Hodgkinson, Mary-Anne Enoch, Vibhuti Srivastava, et al.
Archives of General Psychiatry
|
February 9, 2011
Emotion processing, major depression, and functional genetic variation of neuropeptide Y
Brian J Mickey, Zhifeng Zhou, Mary M Heitzeg, et al.
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of 22
Search research articles
Search
Showing results (181-190 of 213) with videos related to
Sort By:
Page
of 22
European Journal of Human Genetics : EJHG
|
February 28, 2013
Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHL
Nelly Abdelfatah, David A McComiskey, Lance Doucette, et al.
Journal of the American College of Cardiology
|
February 1, 2005
The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5)
Kathy A Hodgkinson, Patrick S Parfrey, Anne S Bassett, et al.
American Journal of Medical Genetics. Part A
|
March 26, 2018
Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome
Lisa D Palmer, Nancy J Butcher, Erik Boot, et al.
BMC Pregnancy and Childbirth
|
December 21, 2017
Blood pressure self-monitoring in pregnancy (BuMP) feasibility study; a qualitative analysis of women's experiences of self-monitoring
Lisa Hinton, Katherine L Tucker, Sheila M Greenfield, et al.
Biological Psychology
|
December 15, 2007
DISC1 is associated with prefrontal cortical gray matter and positive symptoms in schizophrenia
Philip R Szeszko, Colin A Hodgkinson, Delbert G Robinson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
April 19, 2017
New Repeat Polymorphism in the <i>AKT1</i> Gene Predicts Striatal Dopamine D2/D3 Receptor Availability and Stimulant-Induced Dopamine Release in the Healthy Human Brain
Elena Shumay, Corinde E Wiers, Ehsan Shokri-Kojori, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
March 8, 2014
FKBP5 moderates alcohol withdrawal severity: human genetic association and functional validation in knockout mice
Ming-Chyi Huang, Melanie L Schwandt, Julia A Chester, et al.
Molecular Psychiatry
|
November 11, 2021
Strong and weak cross-inheritance of substance use disorders in a nationally representative sample
Haitao Zhang, Bridget F Grant, Colin A Hodgkinson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 28, 2010
Genome-wide association identifies candidate genes that influence the human electroencephalogram
Colin A Hodgkinson, Mary-Anne Enoch, Vibhuti Srivastava, et al.
Archives of General Psychiatry
|
February 9, 2011
Emotion processing, major depression, and functional genetic variation of neuropeptide Y
Brian J Mickey, Zhifeng Zhou, Mary M Heitzeg, et al.
Page
of 22