Melissa Gymrek - Publications

Affiliations: 
2011-2016 UCSD School of Medicine, San Diego, CA, United States 

47 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Jam HZ, Zook JM, Javadzadeh S, Park J, Sehgal A, Gymrek M. Genome-wide profiling of genetic variation at tandem repeat from long reads. Biorxiv : the Preprint Server For Biology. PMID 38328152 DOI: 10.1101/2024.01.20.576266  0.441
2023 Margoliash J, Fuchs S, Li Y, Zhang X, Massarat A, Goren A, Gymrek M. Polymorphic short tandem repeats make widespread contributions to blood and serum traits. Cell Genomics. 3: 100458. PMID 38116119 DOI: 10.1016/j.xgen.2023.100458  0.4
2023 Sehgal A, Ziaei-Jam H, Shen A, Gymrek M. Genome-wide detection of somatic mosaicism at short tandem repeats. Biorxiv : the Preprint Server For Biology. PMID 38045311 DOI: 10.1101/2023.11.22.568371  0.484
2023 English A, Dolzhenko E, Jam HZ, Mckenzie S, Olson ND, De Coster W, Park J, Gu B, Wagner J, Eberle MA, Gymrek M, Chaisson MJP, Zook JM, Sedlazeck FJ. Benchmarking of small and large variants across tandem repeats. Biorxiv : the Preprint Server For Biology. PMID 37961319 DOI: 10.1101/2023.10.29.564632  0.486
2023 Ziaei Jam H, Li Y, DeVito R, Mousavi N, Ma N, Lujumba I, Adam Y, Maksimov M, Huang B, Dolzhenko E, Qiu Y, Kakembo FE, Joseph H, Onyido B, Adeyemi J, ... ... Gymrek M, et al. A deep population reference panel of tandem repeat variation. Nature Communications. 14: 6711. PMID 37872149 DOI: 10.1038/s41467-023-42278-3  0.537
2023 Lundström OS, Adriaan Verbiest M, Xia F, Jam HZ, Zlobec I, Anisimova M, Gymrek M. WebSTR: A Population-wide Database of Short Tandem Repeat Variation in Humans. Journal of Molecular Biology. 435: 168260. PMID 37678708 DOI: 10.1016/j.jmb.2023.168260  0.544
2023 Massarat A, Gymrek M, McStay B, Jónsson H. Human pangenome supports analysis of complex genomic regions. Nature. 617: 256-258. PMID 37165235 DOI: 10.1038/d41586-023-01490-3  0.364
2023 Maksimov MO, Wu C, Ashbrook DG, Villani F, Colonna V, Mousavi N, Ma N, Lu L, Pritchard JK, Goren A, Williams RW, Palmer AA, Gymrek M. A novel quantitative trait locus implicates in the propensity for genome-wide short tandem repeat expansions in mice. Genome Research. PMID 37127331 DOI: 10.1101/gr.277576.122  0.46
2023 Jam HZ, Li Y, DeVito R, Mousavi N, Ma N, Lujumba I, Adam Y, Maksimov M, Huang B, Dolzhenko E, Qiu Y, Kakembo FE, Joseph H, Onyido B, Adeyemi J, ... ... Gymrek M, et al. A deep population reference panel of tandem repeat variation. Biorxiv : the Preprint Server For Biology. PMID 36945429 DOI: 10.1101/2023.03.09.531600  0.537
2023 Massarat AR, Lamkin M, Reeve C, Williams AL, D'Antonio M, Gymrek M. Haptools: a toolkit for admixture and haplotype analysis. Bioinformatics (Oxford, England). PMID 36847450 DOI: 10.1093/bioinformatics/btad104  0.365
2022 Verbiest M, Maksimov M, Jin Y, Anisimova M, Gymrek M, Bilgin Sonay T. Mutation and selection processes regulating short tandem repeats give rise to genetic and phenotypic diversity across species. Journal of Evolutionary Biology. PMID 36289560 DOI: 10.1111/jeb.14106  0.508
2022 Mortazavi M, Ren Y, Saini S, Antaki D, St Pierre CL, Williams A, Sohni A, Wilkinson MF, Gymrek M, Sebat J, Palmer AA. SNPs, short tandem repeats, and structural variants are responsible for differential gene expression across C57BL/6 and C57BL/10 substrains. Cell Genomics. 2. PMID 35720252 DOI: 10.1016/j.xgen.2022.100102  0.392
2022 Sun T, Cruz GI, Mousavi N, Marić I, Brewer A, Wong RJ, Aghaeepour N, Sayed N, Wu JC, Stevenson DK, Leonard SA, Gymrek M, Winn VD. HMOX1 Genetic Polymorphisms Display Ancestral Diversity and May Be Linked to Hypertensive Disorders in Pregnancy. Reproductive Sciences (Thousand Oaks, Calif.). PMID 35697922 DOI: 10.1007/s43032-022-01001-1  0.364
2021 Pinsach-Abuin ML, Del Olmo B, Pérez-Agustin A, Mates J, Allegue C, Iglesias A, Ma Q, Merkurjev D, Konovalov S, Zhang J, Sheikh F, Telenti A, Brugada J, Brugada R, Gymrek M, et al. Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants. Cell Reports. Medicine. 2: 100250. PMID 33948580 DOI: 10.1016/j.xcrm.2021.100250  0.325
2021 Bakhtiari M, Park J, Ding YC, Shleizer-Burko S, Neuhausen SL, Halldórsson BV, Stefánsson K, Gymrek M, Bafna V. Variable number tandem repeats mediate the expression of proximal genes. Nature Communications. 12: 2075. PMID 33824302 DOI: 10.1038/s41467-021-22206-z  0.39
2021 Mitra I, Huang B, Mousavi N, Ma N, Lamkin M, Yanicky R, Shleizer-Burko S, Lohmueller KE, Gymrek M. Patterns of de novo tandem repeat mutations and their role in autism. Nature. 589: 246-250. PMID 33442040 DOI: 10.1038/s41586-020-03078-7  0.416
2020 Mousavi N, Margoliash J, Pusarla N, Saini S, Yanicky R, Gymrek M. TRTools: a toolkit for genome-wide analysis of tandem repeats. Bioinformatics (Oxford, England). PMID 32805020 DOI: 10.1093/Bioinformatics/Btaa736  0.477
2019 Breuss MW, Antaki D, George RD, Kleiber M, James KN, Ball LL, Hong O, Mitra I, Yang X, Wirth SA, Gu J, Garcia CAB, Gujral M, Brandler WM, Musaev D, ... ... Gymrek M, et al. Autism risk in offspring can be assessed through quantification of male sperm mosaicism. Nature Medicine. PMID 31873310 DOI: 10.1038/S41591-019-0711-0  0.402
2019 Fotsing SF, Margoliash J, Wang C, Saini S, Yanicky R, Shleizer-Burko S, Goren A, Gymrek M. The impact of short tandem repeat variation on gene expression. Nature Genetics. 51: 1652-1659. PMID 31676866 DOI: 10.1038/S41588-019-0521-9  0.498
2019 Musa J, Cidre-Aranaz F, Aynaud MM, Orth MF, Knott MML, Mirabeau O, Mazor G, Varon M, Hölting TLB, Grossetête S, Gartlgruber M, Surdez D, Gerke JS, Ohmura S, Marchetto A, ... ... Gymrek M, et al. Cooperation of cancer drivers with regulatory germline variants shapes clinical outcomes. Nature Communications. 10: 4128. PMID 31511524 DOI: 10.1038/S41467-019-12071-2  0.439
2019 Mousavi N, Shleizer-Burko S, Yanicky R, Gymrek M. Profiling the genome-wide landscape of tandem repeat expansions. Nucleic Acids Research. 47: e90. PMID 31194863 DOI: 10.1093/Nar/Gkz501  0.596
2018 Saini S, Mitra I, Mousavi N, Fotsing SF, Gymrek M. A reference haplotype panel for genome-wide imputation of short tandem repeats. Nature Communications. 9: 4397. PMID 30353011 DOI: 10.1038/S41467-018-06694-0  0.465
2018 Bakhtiari M, Shleizer-Burko S, Gymrek M, Bansal V, Bafna V. Targeted genotyping of variable number tandem repeats with adVNTR. Genome Research. PMID 30352806 DOI: 10.1101/Gr.235119.118  0.549
2018 Kaplanis J, Gordon A, Shor T, Weissbrod O, Geiger D, Wahl M, Gershovits M, Markus B, Sheikh M, Gymrek M, Bhatia G, MacArthur DG, Price AL, Erlich Y. Quantitative analysis of population-scale family trees with millions of relatives. Science (New York, N.Y.). PMID 29496957 DOI: 10.1126/Science.Aam9309  0.663
2017 Gymrek M, Willems T, Reich D, Erlich Y. Interpreting short tandem repeat variations in humans using mutational constraint. Nature Genetics. 49: 1495-1501. PMID 28892063 DOI: 10.1038/Ng.3952  0.791
2017 Rusu V, Hoch E, Mercader JM, Tenen DE, Gymrek M, Hartigan CR, DeRan M, von Grotthuss M, Fontanillas P, Spooner A, Guzman G, Deik AA, Pierce KA, Dennis C, Clish CB, et al. Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms. Cell. 170: 199-212.e20. PMID 28666119 DOI: 10.1016/J.Cell.2017.06.011  0.513
2017 Willems T, Zielinski D, Yuan J, Gordon A, Gymrek M, Erlich Y. Genome-wide profiling of heritable and de novo STR variations. Nature Methods. PMID 28436466 DOI: 10.1038/Nmeth.4267  0.772
2017 Gymrek M. A genomic view of short tandem repeats. Current Opinion in Genetics & Development. 44: 9-16. PMID 28213161 DOI: 10.1016/J.Gde.2017.01.012  0.627
2016 Mallick S, Li H, Lipson M, Mathieson I, Gymrek M, Racimo F, Zhao M, Chennagiri N, Nordenfelt S, Tandon A, Skoglund P, Lazaridis I, Sankararaman S, Fu Q, Rohland N, et al. The Simons Genome Diversity Project: 300 genomes from 142 diverse populations. Nature. PMID 27654912 DOI: 10.1038/Nature18964  0.8
2016 Willems T, Gymrek M, Poznik GD, Tyler-Smith C, Erlich Y. Population-Scale Sequencing Data Enable Precise Estimates of Y-STR Mutation Rates. American Journal of Human Genetics. 98: 919-933. PMID 27126583 DOI: 10.1016/J.Ajhg.2016.04.001  0.794
2016 Poznik GD, Xue Y, Mendez FL, Willems TF, Massaia A, Wilson Sayres MA, Ayub Q, McCarthy SA, Narechania A, Kashin S, Chen Y, Banerjee R, Rodriguez-Flores JL, Cerezo M, Shao H, ... Gymrek M, et al. Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences. Nature Genetics. PMID 27111036 DOI: 10.1038/Ng.3559  0.799
2016 Quilez J, Guilmatre A, Garg P, Highnam G, Gymrek M, Erlich Y, Joshi RS, Mittelman D, Sharp AJ. Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humans. Nucleic Acids Research. PMID 27060133 DOI: 10.1093/Nar/Gkw219  0.7
2016 Willems T, Gymrek M, Poznik GD, Tyler-Smith C, Erlich Y. Population-Scale Sequencing Data Enable Precise Estimates of Y-STR Mutation Rates American Journal of Human Genetics. DOI: 10.1016/j.ajhg.2016.04.001  0.747
2015 Gymrek M, Willems T, Guilmatre A, Zeng H, Markus B, Georgiev S, Daly MJ, Price AL, Pritchard JK, Sharp AJ, Erlich Y. Abundant contribution of short tandem repeats to gene expression variation in humans. Nature Genetics. PMID 26642241 DOI: 10.1038/Ng.3461  0.796
2014 Gymrek M. PyBamView: a browser-based application for viewing short read alignments. Bioinformatics (Oxford, England). 30: 3405-7. PMID 25147359 DOI: 10.1093/Bioinformatics/Btu565  0.307
2014 Willems T, Gymrek M, Highnam G, Mittelman D, Erlich Y. The landscape of human STR variation. Genome Research. 24: 1894-904. PMID 25135957 DOI: 10.1101/Gr.177774.114  0.816
2014 Zielinski D, Markus B, Sheikh M, Gymrek M, Chu C, Zaks M, Srinivasan B, Hoffman JD, Aizenbud D, Erlich Y. OTX2 duplication is implicated in hemifacial microsomia. Plos One. 9: e96788. PMID 24816892 DOI: 10.1371/Journal.Pone.0096788  0.789
2014 Breker M, Gymrek M, Moldavski O, Schuldiner M. LoQAtE--Localization and Quantitation ATlas of the yeast proteomE. A new tool for multiparametric dissection of single-protein behavior in response to biological perturbations in yeast. Nucleic Acids Research. 42: D726-30. PMID 24150937 DOI: 10.1093/Nar/Gkt933  0.308
2013 Gymrek M, Erlich Y. Profiling short tandem repeats from short reads. Methods in Molecular Biology (Clifton, N.J.). 1038: 113-35. PMID 23872972 DOI: 10.1007/978-1-62703-514-9_7  0.704
2013 Gymrek M, McGuire AL, Golan D, Halperin E, Erlich Y. Identifying personal genomes by surname inference. Science (New York, N.Y.). 339: 321-4. PMID 23329047 DOI: 10.1126/Science.1229566  0.744
2012 Zielinski D, Gymrek M, Erlich Y. Back to the family: a renewed approach to rare variant studies. Genome Medicine. 4: 97. PMID 23253160 DOI: 10.1186/Gm398  0.758
2012 Gymrek M, Golan D, Rosset S, Erlich Y. lobSTR: A short tandem repeat profiler for personal genomes. Genome Research. 22: 1154-62. PMID 22522390 DOI: 10.1101/Gr.135780.111  0.763
2012 Gymrek M, Golan D, Rosset S, Erlich Y. lobSTR: a novel pipeline for short tandem repeats profiling in personal genomes F1000research. 3. DOI: 10.7490/F1000Research.1090187.1  0.723
2011 Ram O, Goren A, Amit I, Shoresh N, Yosef N, Ernst J, Kellis M, Gymrek M, Issner R, Coyne M, Durham T, Zhang X, Donaghey J, Epstein CB, Regev A, et al. Combinatorial patterning of chromatin regulators uncovered by genome-wide location analysis in human cells. Cell. 147: 1628-39. PMID 22196736 DOI: 10.1016/J.Cell.2011.09.057  0.343
2011 Gymrek M, Erlich Y. Using DNA sequencers as stethoscopes. Genome Medicine. 3: 73. PMID 22103962 DOI: 10.1186/Gm289  0.701
2010 Naegle KM, Gymrek M, Joughin BA, Wagner JP, Welsch RE, Yaffe MB, Lauffenburger DA, White FM. PTMScout, a Web resource for analysis of high throughput post-translational proteomics studies. Molecular & Cellular Proteomics : McP. 9: 2558-70. PMID 20631208 DOI: 10.1074/Mcp.M110.001206  0.313
2010 Goren A, Ozsolak F, Shoresh N, Ku M, Adli M, Hart C, Gymrek M, Zuk O, Regev A, Milos PM, Bernstein BE. Chromatin profiling by directly sequencing small quantities of immunoprecipitated DNA. Nature Methods. 7: 47-9. PMID 19946276 DOI: 10.1038/Nmeth.1404  0.399
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