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Neurotoxicology
|
July 30, 2011
Lack of association between autism and four heavy metal regulatory genes
Sarah E Owens, Marshall L Summar, Kelli K Ryckman, et al.
Human Molecular Genetics
|
August 22, 2013
Advances in the genomics of common eye diseases
Jessica N Cooke Bailey, Lucia Sobrin, Margaret A Pericak-Vance, et al.
Psychiatric Genetics
|
June 5, 2010
PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility
Gary W Beecham, Adam C Naj, John R Gilbert, et al.
Molecular Vision
|
December 30, 2008
Lack of association of polymorphisms in homocysteine metabolism genes with pseudoexfoliation syndrome and glaucoma
Bao Jian Fan, Teresa Chen, Cynthia Grosskreutz, et al.
Annals of Human Genetics
|
September 5, 2012
Identification and confirmation of an exonic splicing enhancer variation in exon 5 of the Alzheimer disease associated PICALM gene
Nathalie C Schnetz-Boutaud, Joshua Hoffman, Jared E Coe, et al.
Journal of Clinical Medicine
|
March 10, 2016
The Application of Genetic Risk Scores in Age-Related Macular Degeneration: A Review
Jessica N Cooke Bailey, Joshua D Hoffman, Rebecca J Sardell, et al.
BMC Medical Genetics
|
May 7, 2004
Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes
Holli B Hutcheson, Lana M Olson, Yuki Bradford, et al.
Epilepsia
|
October 24, 2006
Identification of a novel locus for febrile seizures and epilepsy on chromosome 21q22
Peter Hedera, Shaochun Ma, Marcia A Blair, et al.
Investigative Ophthalmology & Visual Science
|
March 4, 2009
Localization of age-related macular degeneration-associated ARMS2 in cytosol, not mitochondria
Gaofeng Wang, Kylee L Spencer, Brenda L Court, et al.
Circulation
|
April 2, 2008
Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation
Dawood Darbar, Prince J Kannankeril, Brian S Donahue, et al.
Page
of 54
Search research articles
Search
Showing results (61-70 of 537) with videos related to
Sort By:
Page
of 54
Neurotoxicology
|
July 30, 2011
Lack of association between autism and four heavy metal regulatory genes
Sarah E Owens, Marshall L Summar, Kelli K Ryckman, et al.
Human Molecular Genetics
|
August 22, 2013
Advances in the genomics of common eye diseases
Jessica N Cooke Bailey, Lucia Sobrin, Margaret A Pericak-Vance, et al.
Psychiatric Genetics
|
June 5, 2010
PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility
Gary W Beecham, Adam C Naj, John R Gilbert, et al.
Molecular Vision
|
December 30, 2008
Lack of association of polymorphisms in homocysteine metabolism genes with pseudoexfoliation syndrome and glaucoma
Bao Jian Fan, Teresa Chen, Cynthia Grosskreutz, et al.
Annals of Human Genetics
|
September 5, 2012
Identification and confirmation of an exonic splicing enhancer variation in exon 5 of the Alzheimer disease associated PICALM gene
Nathalie C Schnetz-Boutaud, Joshua Hoffman, Jared E Coe, et al.
Journal of Clinical Medicine
|
March 10, 2016
The Application of Genetic Risk Scores in Age-Related Macular Degeneration: A Review
Jessica N Cooke Bailey, Joshua D Hoffman, Rebecca J Sardell, et al.
BMC Medical Genetics
|
May 7, 2004
Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes
Holli B Hutcheson, Lana M Olson, Yuki Bradford, et al.
Epilepsia
|
October 24, 2006
Identification of a novel locus for febrile seizures and epilepsy on chromosome 21q22
Peter Hedera, Shaochun Ma, Marcia A Blair, et al.
Investigative Ophthalmology & Visual Science
|
March 4, 2009
Localization of age-related macular degeneration-associated ARMS2 in cytosol, not mitochondria
Gaofeng Wang, Kylee L Spencer, Brenda L Court, et al.
Circulation
|
April 2, 2008
Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation
Dawood Darbar, Prince J Kannankeril, Brian S Donahue, et al.
Page
of 54