Bogdan Pasaniuc - Google Scholar Citations

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	All	Since 2014
Citations	5073	4615
h-index	35	34
i10-index	61	53

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Co-authors

Alexander (Sasha) GusevDana-Farber Cancer InstituteVerified email at dfci.harvard.edu
Noah A ZaitlenAssociate Professor at UCLAVerified email at ucla.edu
Huwenbo ShiHarvard T.H. Chan School of Public Health; Broad Institute of MIT and HarvardVerified email at hsph.harvard.edu
Gleb KichaevAppleVerified email at apple.com
Nicholas MancusoPost-doctoral Fellow at David Geffen School of Medicine, UCLAVerified email at mednet.ucla.edu
Eleazar EskinUniversity of California, Los AngelesVerified email at cs.ucla.edu
Eran HalperinUniversity of California, Los AngelesVerified email at cs.ucla.edu
Gaurav BhatiaVerified email at mit.edu
Farhad HormozdiariPostdoctoral, Harvard University & Broad InstituteVerified email at hsph.harvard.edu
Sriram SankararamanUCLAVerified email at cs.ucla.edu
Nick PattersonStaff scientist, Broad InstituteVerified email at broadinstitute.org
Ion MandoiuUniversity of ConnecticutVerified email at engr.uconn.edu
Sara LindströmResearch Scientist, Harvard School of Public HealthVerified email at hsph.harvard.edu
Christopher R GignouxColorado Center for Personalized Medicine and Department of BiostatisticsVerified email at ucdenver.edu

Bogdan Pasaniuc

University of California at Los Angeles

Verified email at ucla.edu - Homepage

Computational genomics statistical genetics electronic health records disease studies


Title	Cited by	Year
Integrative approaches for large-scale transcriptome-wide association studies A Gusev, A Ko, H Shi, G Bhatia, W Chong, BWJ Penninx, R Jansen, ... Nature Genetics 48, 245–252, 2016	426	2016
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases A Gusev, SH Lee, G Trynka, H Finucane, BJ Vilhjálmsson, H Xu, C Zang, ... The American Journal of Human Genetics 95 (5), 535-552, 2014	386	2014
Modeling linkage disequilibrium increases accuracy of polygenic risk scores BJ Vilhjálmsson, J Yang, HK Finucane, A Gusev, S Lindström, S Ripke, ... The American Journal of Human Genetics 97 (4), 576-592, 2015	319	2015
Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits N Zaitlen, P Kraft, N Patterson, B Pasaniuc, G Bhatia, S Pollack, AL Price PLoS genetics 9 (5), e1003520, 2013	270	2013
Integrating functional data to prioritize causal variants in statistical fine-mapping studies G Kichaev, WY Yang, S Lindstrom, F Hormozdiari, E Eskin, AL Price, ... PLoS genetics 10 (10), e1004722, 2014	245	2014
Dissecting the genetics of complex traits using summary association statistics B Pasaniuc, AL Price Nature Reviews Genetics, 072934, 2016	194	2016
Identifying causal variants at loci with multiple signals of association F Hormozdiari, E Kostem, EY Kang, B Pasaniuc, E Eskin Genetics 198 (2), 497-508, 2014	179	2014
Fast and accurate inference of local ancestry in Latino populations Y Baran, B Pasaniuc, S Sankararaman, DG Torgerson, C Gignoux, C Eng, ... Bioinformatics 28 (10), 1359-1367, 2012	170	2012
Extremely low-coverage sequencing and imputation increases power for genome-wide association studies B Pasaniuc, N Rohland, PJ McLaren, K Garimella, N Zaitlen, H Li, ... Nature genetics 44 (6), 631, 2012	168	2012
Colocalization of GWAS and eQTL signals detects target genes F Hormozdiari, M Van De Bunt, AV Segre, X Li, JWJ Joo, M Bilow, JH Sul, ... The American Journal of Human Genetics 99 (6), 1245-1260, 2016	160	2016
Contrasting the genetic architecture of 30 complex traits from summary association data H Shi, G Kichaev, B Pasaniuc American Journal of Human Genetics, 035907, 2016	153	2016
New approaches to disease mapping in admixed populations MF Seldin, B Pasaniuc, AL Price Nature Reviews Genetics 12 (8), 523, 2011	134	2011
Inference of locus-specific ancestry in closely related populations B Paşaniuc, S Sankararaman, G Kimmel, E Halperin Bioinformatics 25 (12), i213-i221, 2009	122	2009
Fast and accurate imputation of summary statistics enhances evidence of functional enrichment B Pasaniuc, N Zaitlen, H Shi, G Bhatia, A Gusev, J Pickrell, J Hirschhorn, ... Bioinformatics 30 (20), 2906-2914, 2014	115	2014
Quantifying missing heritability at known GWAS loci A Gusev, G Bhatia, N Zaitlen, BJ Vilhjalmsson, D Diogo, EA Stahl, ... PLoS genetics 9 (12), e1003993, 2013	110	2013
Leveraging genetic variability across populations for the identification of causal variants N Zaitlen, B Paşaniuc, T Gur, E Ziv, E Halperin The American Journal of Human Genetics 86 (1), 23-33, 2010	109	2010
Integrating gene expression with summary association statistics to identify genes associated with 30 complex traits N Mancuso, H Shi, P Goddard, G Kichaev, A Gusev, B Pasaniuc The American Journal of Human Genetics 100 (3), 473-487, 2017	99	2017
Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium B Pasaniuc, N Zaitlen, G Lettre, GK Chen, A Tandon, WHL Kao, ... PLoS genetics 7 (4), e1001371, 2011	99	2011
Inhibition of activated pericentromeric SINE/Alu repeat transcription in senescent human adult stem cells reinstates self-renewal VV Lunyak Cell Cycle 10 (17), 3016-3030, 2011	94	2011
The contribution of rare variation to prostate cancer heritability N Mancuso, N Rohland, KA Rand, A Tandon, A Allen, D Quinque, ... Nature genetics 48 (1), 30, 2016	91	2016

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