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Neurobiology of Aging
|
November 12, 2023
Genetic analyses in multiplex families confirms chromosome 5q35 as a risk locus for Alzheimer's Disease in individuals of African Ancestry
Karen Nuytemans, Farid Rajabli, Melissa Jean-Francois, et al.
Ophthalmology
|
October 25, 2016
Heritability of Choroidal Thickness in the Amish
Rebecca J Sardell, Muneeswar G Nittala, Larry D Adams, et al.
Journal of Alzheimer'S Disease & Parkinsonism
|
November 28, 2017
Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function
H N Cukier, B K Kunkle, K L Hamilton, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
October 12, 2012
The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1
Holly N Cukier, Joycelyn M Lee, Deqiong Ma, et al.
American Journal of Epidemiology
|
June 5, 2010
Variation within DNA repair pathway genes and risk of multiple sclerosis
Farren B S Briggs, Benjamin A Goldstein, Jacob L McCauley, et al.
Human Molecular Genetics
|
April 18, 2015
Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis
Robert A Kozol, Holly N Cukier, Bing Zou, et al.
JAMA Network Open
|
January 20, 2022
Assessment of Clinical Palliative Care Trigger Status vs Actual Needs Among Critically Ill Patients and Their Family Members
Christopher E Cox, Deepshikha Charan Ashana, Krista L Haines, et al.
Genomics
|
April 1, 1996
No genetic effect of alpha1-antichymotrypsin in Alzheimer disease
J L Haines, M L Pritchard, A M Saunders, et al.
Annals of Human Genetics
|
March 6, 2008
Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease
L Wang, E R Hauser, S H Shah, et al.
Human Molecular Genetics
|
March 10, 2010
CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis
Paola G Bronson, Stacy Caillier, Patricia P Ramsay, et al.
Page
of 91
Search research articles
Search
Showing results (611-620 of 908) with videos related to
Sort By:
Page
of 91
Neurobiology of Aging
|
November 12, 2023
Genetic analyses in multiplex families confirms chromosome 5q35 as a risk locus for Alzheimer's Disease in individuals of African Ancestry
Karen Nuytemans, Farid Rajabli, Melissa Jean-Francois, et al.
Ophthalmology
|
October 25, 2016
Heritability of Choroidal Thickness in the Amish
Rebecca J Sardell, Muneeswar G Nittala, Larry D Adams, et al.
Journal of Alzheimer'S Disease & Parkinsonism
|
November 28, 2017
Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function
H N Cukier, B K Kunkle, K L Hamilton, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
October 12, 2012
The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1
Holly N Cukier, Joycelyn M Lee, Deqiong Ma, et al.
American Journal of Epidemiology
|
June 5, 2010
Variation within DNA repair pathway genes and risk of multiple sclerosis
Farren B S Briggs, Benjamin A Goldstein, Jacob L McCauley, et al.
Human Molecular Genetics
|
April 18, 2015
Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis
Robert A Kozol, Holly N Cukier, Bing Zou, et al.
JAMA Network Open
|
January 20, 2022
Assessment of Clinical Palliative Care Trigger Status vs Actual Needs Among Critically Ill Patients and Their Family Members
Christopher E Cox, Deepshikha Charan Ashana, Krista L Haines, et al.
Genomics
|
April 1, 1996
No genetic effect of alpha1-antichymotrypsin in Alzheimer disease
J L Haines, M L Pritchard, A M Saunders, et al.
Annals of Human Genetics
|
March 6, 2008
Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease
L Wang, E R Hauser, S H Shah, et al.
Human Molecular Genetics
|
March 10, 2010
CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis
Paola G Bronson, Stacy Caillier, Patricia P Ramsay, et al.
Page
of 91