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David B Goldstein

Showing results (161-170 of 338) with videos related to

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Nature Genetics|December 8, 2009
Geographical genomics of human leukocyte gene expression variation in southern MoroccoYoussef Idaghdour, Wendy Czika, Kevin V Shianna, et al.
Genome Biology|March 9, 2007
Alternative ion channel splicing in mesial temporal lobe epilepsy and Alzheimer's diseaseErin L Heinzen, Woohyun Yoon, Michael E Weale, et al.
Nature Communications|August 11, 2017
Annotating pathogenic non-coding variants in genic regionsSahar Gelfman, Quanli Wang, K Melodi McSweeney, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2021
High-impact rare genetic variants in severe schizophreniaAnthony W Zoghbi, Ryan S Dhindsa, Terry E Goldberg, et al.
Pharmacogenetics and Genomics|December 14, 2007
Promoter polymorphisms and allelic imbalance in ABCB1 expressionCorinne Loeuillet, Michael Weale, Samuel Deutsch, et al.
The Journal of Allergy and Clinical Immunology|May 19, 2015
Clinical application of whole-genome sequencing in patients with primary immunodeficiencyTalal Mousallem, Thomas J Urban, K Melodi McSweeney, et al.
American Journal of Medical Genetics. Part A|June 10, 2003
Haplotype analysis of the growth hormone releasing hormone receptor locus in three apparently unrelated kindreds from the indian subcontinent with the identical mutation in the GHRH receptorMichael P Wajnrajch, Joseph M Gertner, Alisa S Sokoloff, et al.
JAMA Network Open|October 28, 2022
Risk Variants in the Exomes of Children With Critical IllnessJoshua E Motelow, Natalie C Lippa, Joseph Hostyk, et al.
Medrxiv : the Preprint Server for Health Sciences|October 24, 2023
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies <i>ANTXR2</i> as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.
JAMA Cardiology|December 16, 2020
Assessing the Role of Rare Genetic Variation in Patients With Heart FailureGundula Povysil, Olympe Chazara, Keren J Carss, et al.
Pageof 34

Showing results (161-170 of 338) with videos related to

Sort By:
Pageof 34
Nature Genetics|December 8, 2009
Geographical genomics of human leukocyte gene expression variation in southern MoroccoYoussef Idaghdour, Wendy Czika, Kevin V Shianna, et al.
Genome Biology|March 9, 2007
Alternative ion channel splicing in mesial temporal lobe epilepsy and Alzheimer's diseaseErin L Heinzen, Woohyun Yoon, Michael E Weale, et al.
Nature Communications|August 11, 2017
Annotating pathogenic non-coding variants in genic regionsSahar Gelfman, Quanli Wang, K Melodi McSweeney, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2021
High-impact rare genetic variants in severe schizophreniaAnthony W Zoghbi, Ryan S Dhindsa, Terry E Goldberg, et al.
Pharmacogenetics and Genomics|December 14, 2007
Promoter polymorphisms and allelic imbalance in ABCB1 expressionCorinne Loeuillet, Michael Weale, Samuel Deutsch, et al.
The Journal of Allergy and Clinical Immunology|May 19, 2015
Clinical application of whole-genome sequencing in patients with primary immunodeficiencyTalal Mousallem, Thomas J Urban, K Melodi McSweeney, et al.
American Journal of Medical Genetics. Part A|June 10, 2003
Haplotype analysis of the growth hormone releasing hormone receptor locus in three apparently unrelated kindreds from the indian subcontinent with the identical mutation in the GHRH receptorMichael P Wajnrajch, Joseph M Gertner, Alisa S Sokoloff, et al.
JAMA Network Open|October 28, 2022
Risk Variants in the Exomes of Children With Critical IllnessJoshua E Motelow, Natalie C Lippa, Joseph Hostyk, et al.
Medrxiv : the Preprint Server for Health Sciences|October 24, 2023
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies <i>ANTXR2</i> as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.
JAMA Cardiology|December 16, 2020
Assessing the Role of Rare Genetic Variation in Patients With Heart FailureGundula Povysil, Olympe Chazara, Keren J Carss, et al.
Pageof 34