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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: 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: 0
DOI: 10.1016/j.ajhg.2015.04.004
added
30-Jun-15
2. 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: 2
DOI: 10.1016/j.ajhg.2015.01.003
added
30-Jun-15
3. 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: 0
DOI: 10.1038/ejhg.2014.105
added
30-Jun-15
4. 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
5. 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: 1
DOI: 10.1186/gb-2014-15-6-r88
added
30-Jun-15
6. Title: Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
Author(s): Delaneau, O.; Marchini, J.; Genomes Project, Consortium
Source: Nature Communications Volume: 5 Published: 2014
Times Cited: 2
DOI: 10.1038/ncomms4934
added
30-Jun-15
7. Title: Large numbers of individuals are required to classify and define risk for rare variants in known cancer risk genes
Author(s): Shirts, B. H.; Jacobson, A.; Jarvik, G. P.; et al.
Source: Genetics in Medicine Volume: 16 Issue: 7 Pages: 529-534 Published: 2014
Times Cited: 2
DOI: 10.1038/gim.2013.187
added
30-Jun-15
8. Title: Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent
Author(s): de Candia, Teresa R.; Lee, S. Hong; Yang, Jian; et al.
Source: American Journal of Human Genetics Volume: 93 Issue: 3 Pages: 463-470 Published: SEP 5 2013
Times Cited: 6
DOI: 10.1016/j.ajhg.2013.07.007
added
06-Mar-14
9. Title: Detecting Identity by Descent and Estimating Genotype Error Rates in Sequence Data
Author(s): Browning, Brian L.; Browning, Sharon R.
Source: American Journal of Human Genetics Volume: 93 Issue: 5 Pages: 840-851 Published: NOV 7 2013
Times Cited: 8
DOI: 10.1016/j.ajhg.2013.09.014
added
06-Mar-14
10. Title: Exome Sequencing Reveals Novel Rare Variants in the Ryanodine Receptor and Calcium Channel Genes in Malignant Hyperthermia Families
Author(s): Kim, Jerry H.; Jarvik, Gail P.; Browning, Brian L.; et al.
Source: Anesthesiology Volume: 119 Issue: 5 Pages: 1054-1065 Published: NOV 2013
Times Cited: 7
DOI: 10.1097/ALN.0b013e3182a8a998
added
06-Mar-14
publication(s)  
First Page Previous Page Page   of  7  Go Next Page Last Page
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