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Jennifer E Below

Showing results (71-80 of 147) with videos related to

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HGG Advances|January 20, 2022
Population-based genetic effects for developmental stutteringHannah G Polikowsky, Douglas M Shaw, Lauren E Petty, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|April 13, 2023
A haptoglobin (HP) structural variant alters the effect of APOE alleles on Alzheimer's diseaseHaimeng Bai, Adam C Naj, Penelope Benchek, et al.
BMC Obesity|October 12, 2018
Complex patterns of direct and indirect association between the transcription Factor-7 like 2 gene, body mass index and type 2 diabetes diagnosis in adulthood in the Hispanic Community Health Study/Study of LatinosLindsay Fernández-Rhodes, Annie Green Howard, Mariaelisa Graff, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 2007
Insulin gene mutations as a cause of permanent neonatal diabetesJulie Støy, Emma L Edghill, Sarah E Flanagan, et al.
American Journal of Human Genetics|January 1, 2013
Whole-genome analysis reveals that mutations in inositol polyphosphate phosphatase-like 1 cause opsismodysplasiaJennifer E Below, Dawn L Earl, Kathryn M Shively, et al.
American Journal of Human Genetics|December 28, 2020
Host genetic effects in pneumoniaHung-Hsin Chen, Douglas M Shaw, Lauren E Petty, et al.
American Journal of Human Genetics|October 10, 2025
COMPADRE: Combined pedigree-aware distant relatedness estimation for improved pedigree reconstructionGrahame F Evans, James T Baker, Lauren E Petty, et al.
American Journal of Human Genetics|December 25, 2012
Mutations in ECEL1 cause distal arthrogryposis type 5DMargaret J McMillin, Jennifer E Below, Kathryn M Shively, et al.
Human Molecular Genetics|November 1, 2016
Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation levelHeming Wang, Brian E Cade, Han Chen, et al.
The Journal of Clinical Endocrinology and Metabolism|June 28, 2025
Multi-omics of human obesity and related multi-system diseasesMohammad Yaser Anwar, Heather M Highland, Quanhu Sheng, et al.
Pageof 15

Showing results (71-80 of 147) with videos related to

Sort By:
Pageof 15
HGG Advances|January 20, 2022
Population-based genetic effects for developmental stutteringHannah G Polikowsky, Douglas M Shaw, Lauren E Petty, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|April 13, 2023
A haptoglobin (HP) structural variant alters the effect of APOE alleles on Alzheimer's diseaseHaimeng Bai, Adam C Naj, Penelope Benchek, et al.
BMC Obesity|October 12, 2018
Complex patterns of direct and indirect association between the transcription Factor-7 like 2 gene, body mass index and type 2 diabetes diagnosis in adulthood in the Hispanic Community Health Study/Study of LatinosLindsay Fernández-Rhodes, Annie Green Howard, Mariaelisa Graff, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 2007
Insulin gene mutations as a cause of permanent neonatal diabetesJulie Støy, Emma L Edghill, Sarah E Flanagan, et al.
American Journal of Human Genetics|January 1, 2013
Whole-genome analysis reveals that mutations in inositol polyphosphate phosphatase-like 1 cause opsismodysplasiaJennifer E Below, Dawn L Earl, Kathryn M Shively, et al.
American Journal of Human Genetics|December 28, 2020
Host genetic effects in pneumoniaHung-Hsin Chen, Douglas M Shaw, Lauren E Petty, et al.
American Journal of Human Genetics|October 10, 2025
COMPADRE: Combined pedigree-aware distant relatedness estimation for improved pedigree reconstructionGrahame F Evans, James T Baker, Lauren E Petty, et al.
American Journal of Human Genetics|December 25, 2012
Mutations in ECEL1 cause distal arthrogryposis type 5DMargaret J McMillin, Jennifer E Below, Kathryn M Shively, et al.
Human Molecular Genetics|November 1, 2016
Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation levelHeming Wang, Brian E Cade, Han Chen, et al.
The Journal of Clinical Endocrinology and Metabolism|June 28, 2025
Multi-omics of human obesity and related multi-system diseasesMohammad Yaser Anwar, Heather M Highland, Quanhu Sheng, et al.
Pageof 15