| Year |
Citation |
Score |
| 2019 |
Pearlman A, Rahman MT, Upadhyay K, Loke J, Ostrer H. Ectopic Otoconin 90 expression in triple negative breast cancer cell lines is associated with metastasis functions. Plos One. 14: e0211737. PMID 30763339 DOI: 10.1371/Journal.Pone.0211737 |
0.561 |
|
| 2018 |
Fofanov VY, Upadhyay K, Pearlman A, Loke J, O V, Shao Y, Freedland S, Ostrer H. Rapid Next-Generation Sequencing Method for Prediction of Prostate Cancer Risks. The Journal of Molecular Diagnostics : Jmd. PMID 30553750 DOI: 10.1016/J.Jmoldx.2018.07.007 |
0.579 |
|
| 2018 |
Pearlman A, Upadhyay K, Cole K, Loke J, Sun K, Fineberg S, Freedland SJ, Shao Y, Ostrer H. Robust genomic copy number predictor of pan cancer metastasis. Genes & Cancer. 9: 66-77. PMID 29725504 DOI: 10.18632/Genesandcancer.165 |
0.595 |
|
| 2017 |
Syeda MM, Upadhyay K, Loke J, Pearlman A, Klugman S, Shao Y, Ostrer H. Prediction of breast cancer risk based on flow-variant analysis of circulating peripheral blood B cells. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 28301456 DOI: 10.1038/Gim.2016.222 |
0.533 |
|
| 2015 |
Loke J, Pearlman A, Upadhyay K, Tesfa L, Shao Y, Ostrer H. Functional variant analyses (FVAs) predict pathogenicity in the BRCA1 DNA double-strand break repair pathway. Human Molecular Genetics. 24: 3030-7. PMID 25652403 DOI: 10.1093/Hmg/Ddv048 |
0.547 |
|
| 2014 |
Loke J, Pearlman A, Radi O, Zuffardi O, Giussani U, Pallotta R, Camerino G, Ostrer H. Mutations in MAP3K1 tilt the balance from SOX9/FGF9 to WNT/β-catenin signaling. Human Molecular Genetics. 23: 1073-83. PMID 24135036 DOI: 10.1093/Hmg/Ddt502 |
0.512 |
|
| 2013 |
Zeegers MP, Nekeman D, Khan HS, van Dijk BA, Goldbohm RA, Schalken J, Shajahan S, Pearlman A, Oddoux C, van den Brandt PA, Schouten LJ, Ostrer H. Prostate cancer susceptibility genes on 8p21-23 in a Dutch population. Prostate Cancer and Prostatic Diseases. 16: 248-53. PMID 23628848 DOI: 10.1038/Pcan.2013.9 |
0.58 |
|
| 2013 |
Sarsour K, Greenberg J, Johnston JA, Nelson DR, O'Brien LA, Oddoux C, Ostrer H, Pearlman A, Reed G. The role of the FcGRIIIa polymorphism in modifying the association between treatment and outcome in patients with rheumatoid arthritis treated with rituximab versus TNF-α antagonist therapies. Clinical and Experimental Rheumatology. 31: 189-94. PMID 23294992 |
0.431 |
|
| 2012 |
Pearlman A, Campbell C, Brooks E, Genshaft A, Shajahan S, Ittman M, Bova GS, Melamed J, Holcomb I, Schneider RJ, Ostrer H. Clustering-Based Method for Developing a Genomic Copy Number Alteration Signature for Predicting the Metastatic Potential of Prostate Cancer. Journal of Probability and Statistics. 2012: 873570. PMID 25419216 DOI: 10.1155/2012/873570 |
0.591 |
|
| 2012 |
Campbell CL, Palamara PF, Dubrovsky M, Botigué LR, Fellous M, Atzmon G, Oddoux C, Pearlman A, Hao L, Henn BM, Burns E, Bustamante CD, Comas D, Friedman E, Pe'er I, et al. North African Jewish and non-Jewish populations form distinctive, orthogonal clusters. Proceedings of the National Academy of Sciences of the United States of America. 109: 13865-70. PMID 22869716 DOI: 10.1073/Pnas.1204840109 |
0.509 |
|
| 2012 |
Velez C, Palamara PF, Guevara-Aguirre J, Hao L, Karafet T, Guevara-Aguirre M, Pearlman A, Oddoux C, Hammer M, Burns E, Pe'Er I, Atzmon G, Ostrer H. The impact of Converso Jews on the genomes of modern Latin Americans Human Genetics. 131: 251-263. PMID 21789512 DOI: 10.1007/S00439-011-1072-Z |
0.559 |
|
| 2011 |
Rose AE, Poliseno L, Wang J, Clark M, Pearlman A, Wang G, Vega Y Saenz de Miera EC, Medicherla R, Christos PJ, Shapiro R, Pavlick A, Darvishian F, Zavadil J, Polsky D, Hernando E, et al. Integrative genomics identifies molecular alterations that challenge the linear model of melanoma progression. Cancer Research. 71: 2561-71. PMID 21343389 DOI: 10.1158/0008-5472.Can-10-2958 |
0.555 |
|
| 2011 |
Zeegers MP, Khan HS, Schouten LJ, van Dijk BA, Goldbohm RA, Schalken J, Shajahan S, Pearlman A, Oddoux C, van den Brandt PA, Ostrer H. Genetic marker polymorphisms on chromosome 8q24 and prostate cancer in the Dutch population: DG8S737 may not be the causative variant. European Journal of Human Genetics : Ejhg. 19: 118-20. PMID 20700145 DOI: 10.1038/Ejhg.2010.133 |
0.578 |
|
| 2010 |
Pearlman A, Loke J, Le Caignec C, White S, Chin L, Friedman A, Warr N, Willan J, Brauer D, Farmer C, Brooks E, Oddoux C, Riley B, Shajahan S, Camerino G, et al. Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination. American Journal of Human Genetics. 87: 898-904. PMID 21129722 DOI: 10.1016/J.Ajhg.2010.11.003 |
0.532 |
|
| 2010 |
Kerns SL, Ostrer H, Stock R, Li W, Moore J, Pearlman A, Campbell C, Shao Y, Stone N, Kusnetz L, Rosenstein BS. Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. International Journal of Radiation Oncology, Biology, Physics. 78: 1292-300. PMID 20932654 DOI: 10.1016/J.Ijrobp.2010.07.036 |
0.559 |
|
| 2010 |
Atzmon G, Hao L, Pe'er I, Velez C, Pearlman A, Palamara PF, Morrow B, Friedman E, Oddoux C, Burns E, Ostrer H. Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry. American Journal of Human Genetics. 86: 850-9. PMID 20560205 DOI: 10.1016/J.Ajhg.2010.04.015 |
0.529 |
|
| 2010 |
Refai O, Friedman A, Terry L, Jewett T, Pearlman A, Perle MA, Ostrer H. De novo 12;17 translocation upstream of SOX9 resulting in 46,XX testicular disorder of sex development. American Journal of Medical Genetics. Part A. 152: 422-6. PMID 20082466 DOI: 10.1002/Ajmg.A.33201 |
0.529 |
|
| 2010 |
Rose AE, Poliseno L, Pearlman A, Wang J, Ostrer H, Darvishian F, Shapiro RL, Pavlick AC, Hernando E, Osman I. The use of integrative genomics to define molecular signatures of melanoma histologic subtypes. Journal of Clinical Oncology. 28: 8553-8553. DOI: 10.1200/Jco.2010.28.15_Suppl.8553 |
0.535 |
|
| 2009 |
Rose AE, Wang J, Pearlman A, Doudican N, Hernando E, Orlow SJ, Polsky D, Ostrer H, Osman I. The unique molecular signatures of nodular and superficial spreading melanoma. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 27: 9047. PMID 27962135 DOI: 10.1200/Jco.2009.27.15_Suppl.9047 |
0.503 |
|
| 2009 |
Purushothaman R, Gunturu SD, Anhalt H, Ten S, Friedman A, Pearlman A, Ostrer H. Array comparative genomic hybridization analysis of heritable Xp deletion. American Journal of Medical Genetics. Part A. 149: 529-31. PMID 19213022 DOI: 10.1002/Ajmg.A.32658 |
0.539 |
|
| 2008 |
Fischer I, Cunliffe C, Bollo RJ, Weiner HL, Devinsky O, Ruiz-Tachiquin ME, Venuto T, Pearlman A, Chiriboga L, Schneider RJ, Ostrer H, Miller DC. Glioma-like proliferation within tissues excised as tubers in patients with tuberous sclerosis complex. Acta Neuropathologica. 116: 67-77. PMID 18581125 DOI: 10.1007/S00401-008-0391-1 |
0.53 |
|
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