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Browning, Brian L
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ResearcherID: A-1178-2010
URL: http://www.researcherid.com/rid/A-1178-2010
ORCID: http://orcid.org/0000-0001-6454-6633
My Institutions (more details)
Primary Institution:
Sub-org/Dept: Department of Medicine, Division of Medical Genetics
Role:
 
 

This list contains papers that I have authored.

publication(s)  
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1. Title: Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos
Author(s): Conomos, Matthew P.; Laurie, Cecelia A.; Stilp, Adrienne M.; et al.
Source: American Journal of Human Genetics Volume: 98 Issue: 1 Pages: 165-184 Published: JAN 7 2016
Times Cited: 2
DOI: 10.1016/j.ajhg.2015.12.001
added
16-Jun-16
2. Title: Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans
Author(s): Schick, Ursula M.; Jain, Deepti; Hodonsky, Chani J.; et al.
Source: American Journal of Human Genetics Volume: 98 Issue: 2 Pages: 229-242 Published: FEB 4 2016
Times Cited: 1
DOI: 10.1016/j.ajhg.2015.12.003
added
16-Jun-16
3. Title: Genotype Imputation with Millions of Reference Samples
Author(s): Browning, Brian L.; Browning, Sharon R.
Source: American Journal of Human Genetics Volume: 98 Issue: 1 Pages: 116-126 Published: JAN 7 2016
Times Cited: 1
DOI: 10.1016/j.ajhg.2015.11.020
added
16-Jun-16
4. Title: A global reference for human genetic variation
Author(s): Altshuler, David M.; Durbin, Richard M.; Abecasis, Goncalo R.; et al.
Source: Nature Volume: 526 Issue: 7571 Pages: 68-+ Published: OCT 1 2015
Times Cited: 81
DOI: 10.1038/nature15393
added
16-Jun-16
5. Title: Accurate Non-parametric Estimation of Recent Effective Population Size from Segments of Identity by Descent
Author(s): Browning, Sharon R.; Browning, Brian L.
Source: American Journal of Human Genetics Volume: 97 Issue: 3 Pages: 404-418 Published: SEP 3 2015
Times Cited: 2
DOI: 10.1016/j.ajhg.2015.07.012
added
16-Nov-15
6. Title: Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3
Author(s): Chong, J. X.; Burrage, L. C.; Beck, A. E.; et al.
Source: American Journal of Human Genetics Volume: 96 Issue: 5 Pages: 841-849 Published: 2015
Times Cited: 2
DOI: 10.1016/j.ajhg.2015.04.004
added
30-Jun-15
7. Title: De Novo Mutations in NALCN Cause a Syndrome Characterized by Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay
Author(s): Chong, J. X.; McMillin, M. J.; Shively, K. M.; et al.
Source: American Journal of Human Genetics Volume: 96 Issue: 3 Pages: 462-473 Published: 2015
Times Cited: 12
DOI: 10.1016/j.ajhg.2015.01.003
added
30-Jun-15
8. Title: Genome-wide haplotypic testing in a Finnish cohort identifies a novel association with low-density lipoprotein cholesterol
Author(s): Zhang, Q. S.; Browning, B. L.; Browning, S. R.
Source: European Journal of Human Genetics Volume: 23 Issue: 5 Pages: 672-677 Published: 2015
Times Cited: 1
DOI: 10.1038/ejhg.2014.105
added
30-Jun-15
9. Title: Efficient clustering of identity-by-descent between multiple individuals
Author(s): Qian, Y.; Browning, B. L.; Browning, S. R.
Source: Bioinformatics Volume: 30 Issue: 7 Pages: 915-922 Published: 2014
Times Cited: 0
DOI: 10.1093/bioinformatics/btt734
added
30-Jun-15
10. Title: Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences
Author(s): Colonna, V.; Ayub, Q.; Chen, Y.; et al.
Source: Genome Biology Volume: 15 Issue: 6 Published: 2014
Times Cited: 16
DOI: 10.1186/gb-2014-15-6-r88
added
30-Jun-15
publication(s)  
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