Yaniv Erlich
Yaniv Erlich
MyHeritage CSO and Associate Professor of Computer Science, Columbia University
Verified email at cs.columbia.edu - Homepage
Title
Cited by
Cited by
Year
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68-74, 2015
68192015
Identifying personal genomes by surname inference
M Gymrek, AL McGuire, D Golan, E Halperin, Y Erlich
Science 339 (6117), 321-324, 2013
10042013
The Simons genome diversity project: 300 genomes from 142 diverse populations
S Mallick, H Li, M Lipson, I Mathieson, M Gymrek, F Racimo, M Zhao, ...
Nature 538 (7624), 201-206, 2016
6702016
Routes for breaching and protecting genetic privacy
Y Erlich, A Narayanan
Nature Reviews Genetics 15 (6), 409-421, 2014
3652014
DNA Fountain enables a robust and efficient storage architecture
Y Erlich, D Zielinski
Science 355 (6328), 950-954, 2017
2942017
Hierarchical rules for Argonaute loading in Drosophila
B Czech, R Zhou, Y Erlich, J Brennecke, R Binari, C Villalta, A Gordon, ...
Molecular cell 36 (3), 445-456, 2009
2882009
lobSTR: a short tandem repeat profiler for personal genomes
M Gymrek, D Golan, S Rosset, Y Erlich
Genome research 22 (6), 1154-1162, 2012
2582012
A role for microRNAs in maintenance of mouse mammary epithelial progenitor cells
I Ibarra, Y Erlich, SK Muthuswamy, R Sachidanandam, GJ Hannon
Genes & development 21 (24), 3238-3243, 2007
2392007
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences
GD Poznik, Y Xue, FL Mendez, TF Willems, A Massaia, MAW Sayres, ...
Nature genetics 48 (6), 593-599, 2016
2212016
Alta-Cyclic: a self-optimizing base caller for next-generation sequencing
Y Erlich, PP Mitra, WR McCombie, GJ Hannon
Nature methods 5 (8), 679-682, 2008
2122008
Abundant contribution of short tandem repeats to gene expression variation in humans
M Gymrek, T Willems, A Guilmatre, H Zeng, B Markus, S Georgiev, ...
Nature genetics 48 (1), 22-29, 2016
1932016
Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis
Y Erlich, S Edvardson, E Hodges, S Zenvirt, P Thekkat, A Shaag, T Dor, ...
Genome research 21 (5), 658-664, 2011
1752011
The landscape of human STR variation
T Willems, M Gymrek, G Highnam, D Mittelman, Y Erlich, ...
Genome research 24 (11), 1894-1904, 2014
1712014
DNA Sudoku—harnessing high-throughput sequencing for multiplexed specimen analysis
Y Erlich, K Chang, A Gordon, R Ronen, O Navon, M Rooks, GJ Hannon
Genome research 19 (7), 1243-1253, 2009
1552009
Identity inference of genomic data using long-range familial searches
Y Erlich, T Shor, I Pe’er, S Carmi
Science 362 (6415), 690-694, 2018
1432018
Cell contact-dependent acquisition of cellular and viral nonautonomously encoded small RNAs
O Rechavi, Y Erlich, H Amram, L Flomenblit, FV Karginov, I Goldstein, ...
Genes & development 23 (16), 1971-1979, 2009
1342009
Quantitative analysis of population-scale family trees with millions of relatives
J Kaplanis, A Gordon, T Shor, O Weissbrod, D Geiger, M Wahl, ...
Science 360 (6385), 171-175, 2018
1132018
Case–control association mapping by proxy using family history of disease
JZ Liu, Y Erlich, JK Pickrell
Nature genetics 49 (3), 325, 2017
942017
Joubert syndrome 2 (JBTS2) in Ashkenazi Jews is associated with a TMEM216 mutation
S Edvardson, A Shaag, S Zenvirt, Y Erlich, GJ Hannon, AL Shanske, ...
The American Journal of Human Genetics 86 (1), 93-97, 2010
912010
Genome-wide profiling of heritable and de novo STR variations
T Willems, D Zielinski, A Gordon, M Gymrek, Y Erlich
Nature Methods 14 (6), 590-592, 2017
852017
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