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Benjamin M Neale

Showing results (211-220 of 293) with videos related to

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Nature Communications|July 6, 2018
Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestriesSeyedeh M Zekavat, Sanni Ruotsalainen, Robert E Handsaker, et al.
Nature Neuroscience|December 21, 2019
Publisher Correction: Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock proteinSali M K Farhan, Daniel P Howrigan, Liam E Abbott, et al.
Nature Communications|August 25, 2018
Deep-coverage whole genome sequences and blood lipids among 16,324 individualsPradeep Natarajan, Gina M Peloso, Seyedeh Maryam Zekavat, et al.
The American Journal of Psychiatry|April 20, 2013
High loading of polygenic risk for ADHD in children with comorbid aggressionMarian L Hamshere, Kate Langley, Joanna Martin, et al.
Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
American Journal of Human Genetics|March 26, 2021
Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populationsAlicia R Martin, Elizabeth G Atkinson, Sinéad B Chapman, et al.
Circulation. Cardiovascular Genetics|January 30, 2015
Exome sequencing in suspected monogenic dyslipidemiasNathan O Stitziel, Gina M Peloso, Marianne Abifadel, et al.
American Journal of Human Genetics|September 2, 2022
Genetic structure correlates with ethnolinguistic diversity in eastern and southern AfricaElizabeth G Atkinson, Shareefa Dalvie, Yakov Pichkar, et al.
Nature Genetics|November 6, 2007
Two independent alleles at 6q23 associated with risk of rheumatoid arthritisRobert M Plenge, Chris Cotsapas, Leela Davies, et al.
Nature|January 15, 2024
Author Correction: A genomic mutational constraint map using variation in 76,156 human genomesSiwei Chen, Laurent C Francioli, Julia K Goodrich, et al.
Pageof 30

Showing results (211-220 of 293) with videos related to

Sort By:
Pageof 30
Nature Communications|July 6, 2018
Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestriesSeyedeh M Zekavat, Sanni Ruotsalainen, Robert E Handsaker, et al.
Nature Neuroscience|December 21, 2019
Publisher Correction: Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock proteinSali M K Farhan, Daniel P Howrigan, Liam E Abbott, et al.
Nature Communications|August 25, 2018
Deep-coverage whole genome sequences and blood lipids among 16,324 individualsPradeep Natarajan, Gina M Peloso, Seyedeh Maryam Zekavat, et al.
The American Journal of Psychiatry|April 20, 2013
High loading of polygenic risk for ADHD in children with comorbid aggressionMarian L Hamshere, Kate Langley, Joanna Martin, et al.
Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
American Journal of Human Genetics|March 26, 2021
Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populationsAlicia R Martin, Elizabeth G Atkinson, Sinéad B Chapman, et al.
Circulation. Cardiovascular Genetics|January 30, 2015
Exome sequencing in suspected monogenic dyslipidemiasNathan O Stitziel, Gina M Peloso, Marianne Abifadel, et al.
American Journal of Human Genetics|September 2, 2022
Genetic structure correlates with ethnolinguistic diversity in eastern and southern AfricaElizabeth G Atkinson, Shareefa Dalvie, Yakov Pichkar, et al.
Nature Genetics|November 6, 2007
Two independent alleles at 6q23 associated with risk of rheumatoid arthritisRobert M Plenge, Chris Cotsapas, Leela Davies, et al.
Nature|January 15, 2024
Author Correction: A genomic mutational constraint map using variation in 76,156 human genomesSiwei Chen, Laurent C Francioli, Julia K Goodrich, et al.
Pageof 30