Harry Ostrer - Publications

Affiliations: 
Chemistry New York University, New York, NY, United States 
Area:
Genetics, Bioinformatics Biology, Oncology

167 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
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  0.36
2019 Chamberlin A, Huether R, Machado AZ, Groden M, Liu HM, Upadhyay K, O V, Gomes NL, Lerario AM, Nishi MY, Costa EMF, Mendonca B, Domenice S, Velasco J, Loke J, ... Ostrer H, et al. Mutations in MAP3K1 that cause 46,XY disorders of sex development disrupt distinct structural domains in the protein. Human Molecular Genetics. PMID 30608580 DOI: 10.1093/hmg/ddz002  0.36
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  0.36
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  0.36
2017 diSibio G, Upadhyay K, Meyer P, Oddoux C, Ostrer H. Assessing risk for Mendelian disorders in a Bronx population. Molecular Genetics & Genomic Medicine. 5: 516-523. PMID 28944235 DOI: 10.1002/mgg3.307  0.36
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  0.36
2016 Waldman YY, Biddanda A, Dubrovsky M, Campbell CL, Oddoux C, Friedman E, Atzmon G, Halperin E, Ostrer H, Keinan A. The genetic history of Cochin Jews from India. Human Genetics. PMID 27377974 DOI: 10.1007/s00439-016-1698-y  0.36
2016 Waldman YY, Biddanda A, Davidson NR, Billing-Ross P, Dubrovsky M, Campbell CL, Oddoux C, Friedman E, Atzmon G, Halperin E, Ostrer H, Keinan A. The Genetics of Bene Israel from India Reveals Both Substantial Jewish and Indian Ancestry. Plos One. 11: e0152056. PMID 27010569 DOI: 10.1371/journal.pone.0152056  0.36
2015 Rosenstein BS, Capala J, Efstathiou JA, Hammerbacher J, Kerns SL, Kong FS, Ostrer H, Prior FW, Vikram B, Wong J, Xiao Y. How Will Big Data Improve Clinical and Basic Research in Radiation Therapy? International Journal of Radiation Oncology, Biology, Physics. PMID 26797542 DOI: 10.1016/j.ijrobp.2015.11.009  0.36
2015 Baskovich B, Hiraki S, Oddoux C, Ostrer H, Upadhyay K. Response to Zlotogora and Meiner. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 26656652 DOI: 10.1038/gim.2015.170  0.36
2015 Kerns SL, Kundu S, Oh JH, Singhal SK, Janelsins M, Travis LB, Deasy JO, Janssens AC, Ostrer H, Parliament M, Usmani N, Rosenstein BS. The Prediction of Radiotherapy Toxicity Using Single Nucleotide Polymorphism-Based Models: A Step Toward Prevention. Seminars in Radiation Oncology. 25: 281-91. PMID 26384276 DOI: 10.1016/j.semradonc.2015.05.006  0.36
2015 Baskovich B, Hiraki S, Upadhyay K, Meyer P, Carmi S, Barzilai N, Darvasi A, Ozelius L, Peter I, Cho JH, Atzmon G, Clark L, Yu J, Lencz T, Pe'er I, ... Ostrer H, et al. Expanded genetic screening panel for the Ashkenazi Jewish population. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 26334176 DOI: 10.1038/gim.2015.123  0.36
2015 Ostrer H. The origin of the p.E180 growth hormone receptor gene mutation. Growth Hormone & Igf Research : Official Journal of the Growth Hormone Research Society and the International Igf Research Society. PMID 26277320 DOI: 10.1016/j.ghir.2015.08.003  0.36
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  0.36
2014 Ow TJ, Upadhyay K, Belbin TJ, Prystowsky MB, Ostrer H, Smith RV. Bioinformatics in otolaryngology research. Part two: Other high-throughput platforms in genomics and epigenetics Journal of Laryngology and Otology. 128: 942-947. PMID 25230349 DOI: 10.1017/S0022215114002011  0.36
2014 Ow TJ, Upadhyay K, Belbin TJ, Prystowsky MB, Ostrer H, Smith RV. Bioinformatics in otolaryngology research. Part one: Concepts in DNA sequencing and gene expression analysis Journal of Laryngology and Otology. 128: 848-858. PMID 25225743 DOI: 10.1017/S002221511400200X  0.36
2014 Carmi S, Hui KY, Kochav E, Liu X, Xue J, Grady F, Guha S, Upadhyay K, Ben-Avraham D, Mukherjee S, Bowen BM, Thomas T, Vijai J, Cruts M, Froyen G, ... ... Ostrer H, et al. Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins. Nature Communications. 5: 4835. PMID 25203624 DOI: 10.1038/ncomms5835  0.36
2014 Kerns SL, Guevara-Aguirre J, Andrew S, Geng J, Guevara C, Guevara-Aguirre M, Guo M, Oddoux C, Shen Y, Zurita A, Rosenfeld RG, Ostrer H, Hwa V, Dauber A. A novel variant in CDKN1C is associated with intrauterine growth restriction, short stature, and early-adulthood-onset diabetes. The Journal of Clinical Endocrinology and Metabolism. 99: E2117-22. PMID 25057881 DOI: 10.1210/jc.2014-1949  0.36
2014 Rosenstein BS, West CM, Bentzen SM, Alsner J, Andreassen CN, Azria D, Barnett GC, Baumann M, Burnet N, Chang-Claude J, Chuang EY, Coles CE, Dekker A, De Ruyck K, De Ruysscher D, ... ... Ostrer H, et al. Radiogenomics: radiobiology enters the era of big data and team science. International Journal of Radiation Oncology, Biology, Physics. 89: 709-13. PMID 24969789 DOI: 10.1016/j.ijrobp.2014.03.009  0.36
2014 Vacic V, Ozelius LJ, Clark LN, Bar-Shira A, Gana-Weisz M, Gurevich T, Gusev A, Kedmi M, Kenny EE, Liu X, Mejia-Santana H, Mirelman A, Raymond D, Saunders-Pullman R, Desnick RJ, ... ... Ostrer H, et al. Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes. Human Molecular Genetics. 23: 4693-702. PMID 24842889 DOI: 10.1093/hmg/ddu158  0.36
2014 Ostrer H. Disorders of sex development (DSDs): an update. The Journal of Clinical Endocrinology and Metabolism. 99: 1503-9. PMID 24758178 DOI: 10.1210/jc.2013-3690  0.36
2014 Hiraki S, Rinella ES, Schnabel F, Oratz R, Ostrer H. Cancer risk assessment using genetic panel testing: considerations for clinical application. Journal of Genetic Counseling. 23: 604-17. PMID 24599651 DOI: 10.1007/s10897-014-9695-6  0.36
2014 Kerns SL, Ostrer H, Rosenstein BS. Radiogenomics: using genetics to identify cancer patients at risk for development of adverse effects following radiotherapy. Cancer Discovery. 4: 155-65. PMID 24441285 DOI: 10.1158/2159-8290.CD-13-0197  0.36
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  0.36
2014 Kerns SL, de Ruysscher D, Andreassen CN, Azria D, Barnett GC, Chang-Claude J, Davidson S, Deasy JO, Dunning AM, Ostrer H, Rosenstein BS, West CM, Bentzen SM. STROGAR - STrengthening the Reporting Of Genetic Association studies in Radiogenomics. Radiotherapy and Oncology : Journal of the European Society For Therapeutic Radiology and Oncology. 110: 182-8. PMID 23993398 DOI: 10.1016/j.radonc.2013.07.011  0.36
2013 Cespedes MS, Kerns SL, Holzman RS, McLaren PJ, Ostrer H, Aberg JA. Genetic predictors of cervical dysplasia in African American HIV-infected women: ACTG DACS 268. Hiv Clinical Trials. 14: 292-302. PMID 24334182 DOI: 10.1310/hct1406-292  0.36
2013 Isakov O, Rinella ES, Olchovsky D, Shimon I, Ostrer H, Shomron N, Friedman E. Missense mutation in the MEN1 gene discovered through whole exome sequencing co-segregates with familial hyperparathyroidism. Genetics Research. 95: 114-20. PMID 24074368 DOI: 10.1017/S0016672313000141  0.36
2013 Ostrer H. Genes: US patent rulings will fuel invention. Nature. 499: 29. PMID 23823784 DOI: 10.1038/499029a  0.36
2013 Botigué LR, Henn BM, Gravel S, Maples BK, Gignoux CR, Corona E, Atzmon G, Burns E, Ostrer H, Flores C, Bertranpetit J, Comas D, Bustamante CD. Gene flow from North Africa contributes to differential human genetic diversity in southern Europe. Proceedings of the National Academy of Sciences of the United States of America. 110: 11791-6. PMID 23733930 DOI: 10.1073/pnas.1306223110  0.36
2013 Kerns SL, Stock RG, Stone NN, Blacksburg SR, Rath L, Vega A, Fachal L, Gómez-Caamaño A, De Ruysscher D, Lammering G, Parliament M, Blackshaw M, Sia M, Cesaretti J, Terk M, ... ... Ostrer H, et al. Genome-wide association study identifies a region on chromosome 11q14.3 associated with late rectal bleeding following radiation therapy for prostate cancer. Radiotherapy and Oncology : Journal of the European Society For Therapeutic Radiology and Oncology. 107: 372-6. PMID 23719583 DOI: 10.1016/j.radonc.2013.05.001  0.36
2013 Sparano JA, Ostrer H, Kenny PA. Translating genomic research into clinical practice: promise and pitfalls. American Society of Clinical Oncology Educational Book / Asco. American Society of Clinical Oncology. Meeting. 15-23. PMID 23714445 DOI: 10.1200/EdBook_AM.2013.33.15  0.36
2013 Rinella ES, Still C, Shao Y, Wood GC, Chu X, Salerno B, Gerhard GS, Ostrer H. Genome-wide association of single-nucleotide polymorphisms with weight loss outcomes after Roux-en-Y gastric bypass surgery. The Journal of Clinical Endocrinology and Metabolism. 98: E1131-6. PMID 23633212 DOI: 10.1210/jc.2012-3421  0.36
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  0.36
2013 Kerns SL, Stone NN, Stock RG, Rath L, Ostrer H, Rosenstein BS. A 2-stage genome-wide association study to identify single nucleotide polymorphisms associated with development of urinary symptoms after radiotherapy for prostate cancer. The Journal of Urology. 190: 102-8. PMID 23376709 DOI: 10.1016/j.juro.2013.01.096  0.36
2013 Rinella ES, Shao Y, Yackowski L, Pramanik S, Oratz R, Schnabel F, Guha S, LeDuc C, Campbell CL, Klugman SD, Terry MB, Senie RT, Andrulis IL, Daly M, John EM, ... ... Ostrer H, et al. Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation. Human Genetics. 132: 523-36. PMID 23354978 DOI: 10.1007/s00439-013-1269-4  0.36
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  0.36
2013 Ostrer H, Skorecki K. The population genetics of the Jewish people. Human Genetics. 132: 119-27. PMID 23052947 DOI: 10.1007/s00439-012-1235-6  0.36
2013 Kerns SL, Stock R, Stone N, Buckstein M, Shao Y, Campbell C, Rath L, De Ruysscher D, Lammering G, Hixson R, Cesaretti J, Terk M, Ostrer H, Rosenstein BS. A 2-stage genome-wide association study to identify single nucleotide polymorphisms associated with development of erectile dysfunction following radiation therapy for prostate cancer. International Journal of Radiation Oncology, Biology, Physics. 85: e21-8. PMID 23021708 DOI: 10.1016/j.ijrobp.2012.08.003  0.36
2013 Parikh M, Hetherington J, Sheth S, Seiler J, Ostrer H, Gerhard G, Wood C, Still C. Frequencies of obesity susceptibility alleles among ethnically and racially diverse bariatric patient populations. Surgery For Obesity and Related Diseases : Official Journal of the American Society For Bariatric Surgery. 9: 436-41. PMID 22695173 DOI: 10.1016/j.soard.2012.04.004  0.36
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  0.36
2012 Brisbin A, Bryc K, Byrnes J, Zakharia F, Omberg L, Degenhardt J, Reynolds A, Ostrer H, Mezey JG, Bustamante CD. PCAdmix: principal components-based assignment of ancestry along each chromosome in individuals with admixed ancestry from two or more populations. Human Biology. 84: 343-64. PMID 23249312 DOI: 10.3378/027.084.0401  0.36
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, ... Ostrer H, 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  0.36
2012 Marbach D, Costello JC, Küffner R, Vega NM, Prill RJ, Camacho DM, Allison KR, Kellis M, Collins JJ, Stolovitzky G. Wisdom of crowds for robust gene network inference. Nature Methods. 9: 796-804. PMID 22796662 DOI: 10.1038/nmeth.2016  0.36
2012 Kenny EE, Pe'er I, Karban A, Ozelius L, Mitchell AA, Ng SM, Erazo M, Ostrer H, Abraham C, Abreu MT, Atzmon G, Barzilai N, Brant SR, Bressman S, Burns ER, et al. A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. Plos Genetics. 8: e1002559. PMID 22412388 DOI: 10.1371/journal.pgen.1002559  0.36
2012 Loke J, Ostrer H. Rapidly screening variants of uncertain significance in the MAP3K1 gene for phenotypic effects. Clinical Genetics. 81: 272-7. PMID 22171599 DOI: 10.1111/j.1399-0004.2011.01834.x  0.36
2012 Guevara-Aguirre J, Guevara-Aguirre M, Hwa V, Prócel P, Saavedra J, Ostrer H, Fang P, Rosenfeld RG, Kerns S, Rosenbloom AL. Intrauterine and postnatal growth failure with normal GH/IGF1 axis and insulin-resistant diabetes in a consanguineous kinship. European Journal of Endocrinology / European Federation of Endocrine Societies. 166: 521-9. PMID 22170795 DOI: 10.1530/EJE-11-0769  0.36
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  0.36
2011 Ostrer H. Changing the game with whole exome sequencing. Clinical Genetics. 80: 101-3. PMID 21749364 DOI: 10.1111/j.1399-0004.2011.01712.x  0.36
2011 Warr N, Bogani D, Siggers P, Brixey R, Tateossian H, Dopplapudi A, Wells S, Cheeseman M, Xia Y, Ostrer H, Greenfield A. Minor abnormalities of testis development in mice lacking the gene encoding the MAPK signalling component, MAP3K1. Plos One. 6: e19572. PMID 21559298 DOI: 10.1371/journal.pone.0019572  0.36
2011 Moorjani P, Patterson N, Hirschhorn JN, Keinan A, Hao L, Atzmon G, Burns E, Ostrer H, Price AL, Reich D. The history of African gene flow into Southern Europeans, Levantines, and Jews. Plos Genetics. 7: e1001373. PMID 21533020 DOI: 10.1371/journal.pgen.1001373  0.36
2011 Mendez FL, Karafet TM, Krahn T, Ostrer H, Soodyall H, Hammer MF. Increased resolution of Y chromosome haplogroup T defines relationships among populations of the Near East, Europe, and Africa. Human Biology. 83: 39-53. PMID 21453003 DOI: 10.3378/027.083.0103  0.36
2011 Kaklamani V, Yi N, Zhang K, Sadim M, Offit K, Oddoux C, Ostrer H, Mantzoros C, Pasche B. Polymorphisms of ADIPOQ and ADIPOR1 and prostate cancer risk. Metabolism: Clinical and Experimental. 60: 1234-43. PMID 21397927 DOI: 10.1016/j.metabol.2011.01.005  0.36
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, ... Ostrer H, 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  0.36
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  0.36
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, ... ... Ostrer H, 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  0.36
2010 Greenfield A, Madar A, Ostrer H, Bonneau R. DREAM4: Combining genetic and dynamic information to identify biological networks and dynamical models. Plos One. 5: e13397. PMID 21049040 DOI: 10.1371/journal.pone.0013397  0.36
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  0.36
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  0.36
2010 Bryc K, Velez C, Karafet T, Moreno-Estrada A, Reynolds A, Auton A, Hammer M, Bustamante CD, Ostrer H. Colloquium paper: genome-wide patterns of population structure and admixture among Hispanic/Latino populations. Proceedings of the National Academy of Sciences of the United States of America. 107: 8954-61. PMID 20445096 DOI: 10.1073/pnas.0914618107  0.36
2010 Ligr M, Li Y, Zou X, Daniels G, Melamed J, Peng Y, Wang W, Wang J, Ostrer H, Pagano M, Wang Z, Garabedian MJ, Lee P. Tumor suppressor function of androgen receptor coactivator ARA70alpha in prostate cancer. The American Journal of Pathology. 176: 1891-900. PMID 20167864 DOI: 10.2353/ajpath.2010.090293  0.36
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  0.36
2009 Valenzuela CD, Moore HG, Huang WC, Reich EW, Yee H, Ostrer H, Pachter HL. Three synchronous primary carcinomas in a patient with HNPCC associated with a novel germline mutation in MLH1: Case report. World Journal of Surgical Oncology. 7: 94. PMID 19995443 DOI: 10.1186/1477-7819-7-94  0.36
2009 Madar A, Greenfield A, Ostrer H, Vanden-Eijnden E, Bonneau R. The Inferelator 2.0: a scalable framework for reconstruction of dynamic regulatory network models. Conference Proceedings : ... Annual International Conference of the Ieee Engineering in Medicine and Biology Society. Ieee Engineering in Medicine and Biology Society. Annual Conference. 2009: 5448-51. PMID 19964678 DOI: 10.1109/IEMBS.2009.5334018  0.36
2009 Bogani D, Siggers P, Brixey R, Warr N, Beddow S, Edwards J, Williams D, Wilhelm D, Koopman P, Flavell RA, Chi H, Ostrer H, Wells S, Cheeseman M, Greenfield A. Loss of mitogen-activated protein kinase kinase kinase 4 (MAP3K4) reveals a requirement for MAPK signalling in mouse sex determination. Plos Biology. 7: e1000196. PMID 19753101 DOI: 10.1371/journal.pbio.1000196  0.36
2009 Firoz EF, Warycha M, Zakrzewski J, Pollens D, Wang G, Shapiro R, Berman R, Pavlick A, Manga P, Ostrer H, Celebi JT, Kamino H, Darvishian F, Rolnitzky L, Goldberg JD, et al. Association of MDM2 SNP309, age of onset, and gender in cutaneous melanoma. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 15: 2573-80. PMID 19318491 DOI: 10.1158/1078-0432.CCR-08-2678  0.36
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  0.36
2009 Hathaway F, Burns E, Ostrer H. Consumers' desire towards current and prospective reproductive genetic testing. Journal of Genetic Counseling. 18: 137-46. PMID 19160030 DOI: 10.1007/s10897-008-9199-3  0.36
2008 Burri RJ, Stock RG, Cesaretti JA, Atencio DP, Peters S, Peters CA, Fan G, Stone NN, Ostrer H, Rosenstein BS. Association of single nucleotide polymorphisms in SOD2, XRCC1 and XRCC3 with susceptibility for the development of adverse effects resulting from radiotherapy for prostate cancer. Radiation Research. 170: 49-59. PMID 18582155 DOI: 10.1667/RR1219.1  0.36
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  0.36
2008 Kaklamani VG, Sadim M, Hsi A, Offit K, Oddoux C, Ostrer H, Ahsan H, Pasche B, Mantzoros C. Variants of the adiponectin and adiponectin receptor 1 genes and breast cancer risk. Cancer Research. 68: 3178-84. PMID 18451143 DOI: 10.1158/0008-5472.CAN-08-0533  0.36
2008 Gordon E, Panaghie G, Deng L, Bee KJ, Roepke TK, Krogh-Madsen T, Christini DJ, Ostrer H, Basson CT, Chung W, Abbott GW. A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalance. Cardiovascular Research. 77: 98-106. PMID 18006462 DOI: 10.1093/cvr/cvm030  0.36
2008 Peters CA, Stock RG, Cesaretti JA, Atencio DP, Peters S, Burri RJ, Stone NN, Ostrer H, Rosenstein BS. TGFB1 single nucleotide polymorphisms are associated with adverse quality of life in prostate cancer patients treated with radiotherapy. International Journal of Radiation Oncology, Biology, Physics. 70: 752-9. PMID 17689884 DOI: 10.1016/j.ijrobp.2007.05.023  0.36
2008 Ostrer H. Genetic Testing for the Practitioner Essentials of Medical Genomics: Second Edition. 127-141. DOI: 10.1002/9780470336168.ch6  0.36
2007 Ostrer H, Huang HY, Masch RJ, Shapiro E. A cellular study of human testis development. Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation. 1: 286-92. PMID 18391539 DOI: 10.1159/000108930  0.36
2007 Grau JB, Pirelli L, Yu PJ, Galloway AC, Ostrer H. The genetics of mitral valve prolapse Clinical Genetics. 72: 288-295. PMID 17850623 DOI: 10.1111/j.1399-0004.2007.00865.x  0.36
2007 Greenberg JD, Ostrer H. Predicting response to TNF antagonists in rheumatoid arthritis: the promise of pharmacogenetics research using clinical registries. Bulletin of the Nyu Hospital For Joint Diseases. 65: 139-42. PMID 17581108  0.36
2006 Ostrer H, Wilson DI, Hanley NA. Developmental biology: Frontiers for clinical genetics. Human enbryo and early fetus research Clinical Genetics. 70: 98-107. PMID 16879189 DOI: 10.1111/j.1399-0004.2006.00640.x  0.36
2005 Zeegers MP, Ostrer H. Genes in the polyamine biosynthesis pathway may be involved in prostate cancer susceptibility. Future Oncology (London, England). 1: 683-8. PMID 16556045 DOI: 10.2217/14796694.1.5.683  0.36
2005 Shapiro E, Huang H, Masch RJ, McFadden DE, Wu XR, Ostrer H. Immunolocalization of androgen receptor and estrogen receptors alpha and beta in human fetal testis and epididymis. The Journal of Urology. 174: 1695-8; discussion 1. PMID 16148684 DOI: 10.1097/01.ju.0000179540.28209.de  0.36
2005 Kaklamani VG, Baddi L, Liu J, Rosman D, Phukan S, Bradley C, Hegarty C, McDaniel B, Rademaker A, Oddoux C, Ostrer H, Michel LS, Huang H, Chen Y, Ahsan H, et al. Combined genetic assessment of transforming growth factor-beta signaling pathway variants may predict breast cancer risk. Cancer Research. 65: 3454-61. PMID 15833881 DOI: 10.1158/0008-5472.CAN-04-2961  0.36
2005 Reich E, Ostrer H. Genetic Counseling for Patients with Breast Cancer and Their Families Breast Cancer. 319-330. DOI: 10.1016/B978-0-443-06634-4.50023-6  0.36
2004 Daruwala RS, Rudra A, Ostrer H, Lucito R, Wigler M, Mishra B. A versatile statistical analysis algorithm to detect genome copy number variation. Proceedings of the National Academy of Sciences of the United States of America. 101: 16292-7. PMID 15534219 DOI: 10.1073/pnas.0407247101  0.36
2004 Zeegers MP, Kiemeney LA, Nieder AM, Ostrer H. How strong is the association between CAG and GGN repeat length polymorphisms in the androgen receptor gene and prostate cancer risk? Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 13: 1765-71. PMID 15533905  0.36
2004 Kaklamani V, Baddi L, Rosman D, Liu J, Ellis N, Oddoux C, Ostrer H, Chen Y, Ahsan H, Offit K, Pasche B. No major association between TGFBR1*6A and prostate cancer. Bmc Genetics. 5: 28. PMID 15385056 DOI: 10.1186/1471-2156-5-28  0.36
2004 Salman M, Jhanwar SC, Ostrer H. Will the new cytogenetics replace the old cytogenetics? Clinical Genetics. 66: 265-275. PMID 15355426 DOI: 10.1111/j.1399-0004.2004.00316.x  0.36
2004 Jiang S, Gitlin J, Deng FM, Liang FX, Lee A, Atala A, Bauer SB, Ehrlich GD, Feather SA, Goldberg JD, Goodship JA, Goodship TH, Hermanns M, Hu FZ, Jones KE, ... ... Ostrer H, et al. Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity. Kidney International. 66: 10-9. PMID 15200408 DOI: 10.1111/j.1523-1755.2004.00703.x  0.36
2004 Olson SH, Carlson MDA, Ostrer H, Harlap S, Stone A, Winters M, Ambrosone CB. Genetic variants in SOD2, MPO, and NQO1, and risk of ovarian cancer Gynecologic Oncology. 93: 615-620. PMID 15196853 DOI: 10.1016/j.ygyno.2004.03.027  0.36
2004 Fitzgerald T, Duva S, Ostrer H, Pass K, Oddoux C, Ruben R, Caggana M. The frequency of GJB2 and GJB6 mutations in the New York State newborn population: Feasibility of genetic screening for hearing defects Clinical Genetics. 65: 338-342. PMID 15025729 DOI: 10.1111/j.1399-0004.2004.00233.x  0.36
2004 Zeegers MP, van Poppel F, Vlietinck R, Spruijt L, Ostrer H. Founder mutations among the Dutch. European Journal of Human Genetics : Ejhg. 12: 591-600. PMID 15010701 DOI: 10.1038/sj.ejhg.5201151  0.36
2004 Ostrer H. Alterations of sex differentiation in males: from candidate genes to diagnosis and treatments. Current Pharmaceutical Design. 10: 501-11. PMID 14965335 DOI: 10.2174/1381612043453207  0.36
2004 Behar DM, Garrigan D, Kaplan ME, Mobasher Z, Rosengarten D, Karafet TM, Quintana-Murci L, Ostrer H, Skorecki K, Hammer MF. Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations. Human Genetics. 114: 354-65. PMID 14740294 DOI: 10.1007/s00439-003-1073-7  0.36
2003 Jawaheer D, Juo SHH, Le Caignec C, David A, Petit C, Gregersen P, Dowbak S, Damle A, McElreavey K, Ostrer H. Mapping a gene for 46,XY gonadal dysgenesis by linkage analysis Clinical Genetics. 63: 530-535. PMID 12786760 DOI: 10.1034/j.1399-0004.2003.00082.x  0.36
2003 Ben-Yosef T, Ness SL, Madeo AC, Bar-Lev A, Wolfman JH, Ahmed ZM, Desnick RJ, Willner JP, Avraham KB, Ostrer H, Oddoux C, Griffith AJ, Friedman TB. A mutation of PCDH15 among Ashkenazi Jews with the type 1 Usher syndrome. The New England Journal of Medicine. 348: 1664-70. PMID 12711741 DOI: 10.1056/NEJMoa021502  0.36
2003 Nieder AM, Taneja SS, Zeegers MP, Ostrer H. Genetic counseling for prostate cancer risk. Clinical Genetics. 63: 169-76. PMID 12694223 DOI: 10.1034/j.1399-0004.2003.00038.x  0.36
2003 Zeegers MP, Jellema A, Ostrer H. Empiric risk of prostate carcinoma for relatives of patients with prostate carcinoma: a meta-analysis. Cancer. 97: 1894-903. PMID 12673715 DOI: 10.1002/cncr.11262  0.36
2002 Ortenberg J, Oddoux C, Craver R, McElreavey K, Salas-Cortes L, Guillen-Navarro E, Ostrer H, Sarafoglou K, Clarke V, Yee H. SRY gene expression in the ovotestes of XX true hermaphrodites. The Journal of Urology. 167: 1828-31. PMID 11912443  0.36
2002 Kurima K, Peters LM, Yang Y, Riazuddin S, Ahmed ZM, Naz S, Arnaud D, Drury S, Mo J, Makishima T, Ghosh M, Menon PS, Deshmukh D, Oddoux C, Ostrer H, et al. Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function. Nature Genetics. 30: 277-84. PMID 11850618 DOI: 10.1038/ng842  0.36
2001 Ostrer H. Identifying genes for male sex determination in humans Journal of Experimental Zoology. 290: 567-573. PMID 11748605 DOI: 10.1002/jez.1107  0.36
2001 Ostrer H. A genetic profile of contemporary Jewish populations Nature Reviews Genetics. 2: 891-898. PMID 11715044 DOI: 10.1038/35098506  0.36
2001 Ostrer H. Genome and hormones: Gender differences in physiology invited review: Sex-based differences in gene expression Journal of Applied Physiology. 91: 2384-2388. PMID 11641384  0.36
2001 Ostrer H. Sex determination: Lessons from families and embryos Clinical Genetics. 59: 207-215. PMID 11298673 DOI: 10.1034/j.1399-0004.2001.590401.x  0.36
2000 Ostrer H. Sexual differentiation Seminars in Reproductive Medicine. 18: 41-49. PMID 11299518  0.36
2000 Hammer MF, Redd AJ, Wood ET, Bonner MR, Jarjanazi H, Karafet T, Santachiara-Benerecetti S, Oppenheim A, Jobling MA, Jenkins T, Ostrer H, Bonne-Tamir B. Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes. Proceedings of the National Academy of Sciences of the United States of America. 97: 6769-74. PMID 10801975 DOI: 10.1073/pnas.100115997  0.36
2000 Hanley NA, Hagan DM, Clement-Jones M, Ball SG, Strachan T, Salas-Cortés L, McElreavey K, Lindsay S, Robson S, Bullen P, Ostrer H, Wilson DI. SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development Mechanisms of Development. 91: 403-407. PMID 10704874 DOI: 10.1016/S0925-4773(99)00307-X  0.36
2000 Sarafoglou K, Ostrer H. Clinical review 111: Familial sex reversal - A review Journal of Clinical Endocrinology and Metabolism. 85: 483-493. PMID 10690846 DOI: 10.1210/jc.85.2.483  0.36
1999 Oddoux C, Guillen-Navarro E, Ditivoli C, Dicave E, Cilio MR, Clayton CM, Nelson H, Sarafoglou K, McCain N, Peretz H, Seligsohn U, Luzzatto L, Nafa K, Nardi M, Karpatkin M, ... ... Ostrer H, et al. Mendelian diseases among Roman Jews: Implications for the origins of disease alleles Journal of Clinical Endocrinology and Metabolism. 84: 4405-4409. PMID 10599695  0.36
1999 Pasche B, Kolachana P, Nafa K, Satagopan J, Chen YG, Lo RS, Brener D, Yang D, Kirstein L, Oddoux C, Ostrer H, Vineis P, Varesco L, Jhanwar S, Luzzatto L, et al. TβR-I(6A) is a candidate tumor susceptibility allele Cancer Research. 59: 5678-5682. PMID 10582683  0.36
1999 Hanley NA, Ball SG, Clement-Jones M, Hagan DM, Strachan T, Lindsay S, Robson S, Ostrer H, Parker KL, Wilson DI. Expression of steroidogenic factor 1 and Wilms' tumour 1 during early human gonadal development and sex determination. Mechanisms of Development. 87: 175-80. PMID 10495282 DOI: 10.1016/S0925-4773(99)00123-9  0.36
1999 Ostrer H. Sex-based differences in gene transmission and gene expression Lupus. 8: 365-369. PMID 10455514  0.36
1999 Oddoux C, Clayton CM, Nelson HR, Ostrer H. Prevalence of Bloom syndrome heterozygotes among Ashkenazi Jews [10] American Journal of Human Genetics. 64: 1241-1243. PMID 10090915 DOI: 10.1086/302312  0.36
1999 Aksentijevich I, Torosyan Y, Samuels J, Centola M, Pras E, Chae JJ, Oddoux C, Wood G, Azzaro MP, Palumbo G, Giustolisi R, Pras M, Ostrer H, Kastner DL. Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population American Journal of Human Genetics. 64: 949-962. PMID 10090880 DOI: 10.1086/302327  0.36
1998 Ostrer H, Pullarkat RK, Kazmi MA. Glycosylation and palmitoylation are not required for the formation of the X-linked cone opsin visual pigments Molecular Vision. 4: 28. PMID 9852167  0.36
1998 Guillén-Navarro E, Wallerstein R, Reich E, Zajac L, Ostrer H. Acro-renal-ocular syndrome: Expansion of the phenotype Clinical Dysmorphology. 7: 243-248. PMID 9823489  0.36
1998 Morell RJ, Kim HJ, Hood LJ, Goforth L, Friderici K, Fisher R, Van Camp G, Berlin CI, Oddoux C, Ostrer H, Keats B, Friedman TB. Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness. The New England Journal of Medicine. 339: 1500-5. PMID 9819448 DOI: 10.1056/NEJM199811193392103  0.36
1998 Teebi AS, Miller S, Ostrer H, Eydoux P, Colomb-Brockmann C, Oudjhane K, Watters G. Spastic paraplegia, optic atrophy, microcephaly with normal intelligence, and XY sex reversal: A new autosomal recessive syndrome? Journal of Medical Genetics. 35: 759-762. PMID 9733035  0.36
1998 Stephens JC, Reich DE, Goldstein DB, Shin HD, Smith MW, Carrington M, Winkler C, Huttley GA, Allikmets R, Schriml L, Gerrard B, Malasky M, Ramos MD, Morlot S, Tzetis M, ... ... Ostrer H, et al. Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes. American Journal of Human Genetics. 62: 1507-15. PMID 9585595 DOI: 10.1086/301867  0.36
1998 Kronn D, Jansen V, Ostrer H. Carrier screening for cystic fibrosis, Gaucher disease, and Tay-Sachs disease in the Ashkenazi Jewish population: the first 1000 cases at New York University Medical Center, New York, NY. Archives of Internal Medicine. 158: 777-81. PMID 9554684 DOI: 10.1001/archinte.158.7.777  0.36
1998 Ostrer H, Scheuermann RH, Picker LJ. Benefits and dangers of genetic tests [4] Nature. 392: 14. PMID 9510238  0.36
1997 Ostrer H, Kazmi MA. Mutation of a conserved proline disrupts the retinal-binding pocket of the X-linked cone opsins Molecular Vision. 3: 16. PMID 9479007  0.36
1997 Sculerati N, Perle MA, Oddoux C, Clayton CM, Ostrer H. X-inactivation and cytogenetic studies in a family with sensorineural hearing loss and Turner syndrome Otolaryngology - Head and Neck Surgery. 117. PMID 9419154 DOI: 10.1016/S0194-5998(97)70108-6  0.36
1997 Wistinghausen B, Reischer A, Oddoux C, Ostrer H, Nardi M, Karpatkin M. Severe factor XI deficiency in an Arab family associated with a novel mutation in exon 11 British Journal of Haematology. 99: 575-577. PMID 9401068  0.36
1997 Guillén-Navarro E, Wallerstein R, Reich E, Zajac L, Ostrer H. Robinow syndrome with developmental brain dysplasia American Journal of Medical Genetics. 73: 98-99. PMID 9375934  0.36
1997 Laken SJ, Petersen GM, Gruber SB, Oddoux C, Ostrer H, Giardiello FM, Hamilton SR, Hampel H, Markowitz A, Klimstra D, Jhanwar S, Winawer S, Offit K, Luce MC, Kinzler KW, et al. Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC Nature Genetics. 17: 79-83. PMID 9288102 DOI: 10.1038/ng0997-79  0.36
1997 Kazmi MA, Sakmar TP, Ostrer H. Mutation of a conserved cysteine in the X-linked cone opsins causes color vision deficiencies by disrupting protein folding and stability Investigative Ophthalmology and Visual Science. 38: 1074-1081. PMID 9152227  0.36
1997 Veitia R, Ion A, Barbaux S, Jobling MA, Souleyreau N, Ennis K, Ostrer H, Tosi M, Meo T, Chibani J, Fellous M, McElreavey K. Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotype. Human Genetics. 99: 648-52. PMID 9150734 DOI: 10.1007/s004390050422  0.36
1996 Fuqua JS, Sher ES, Fechner PY, Ostrer H, Oddeux C, Schafer AJ, Rosales TO, Migeon CJ, Berkovitz GD. Linkage analysis of a kindred with inherited 46,XY partial gonadal dysgenesis. The Journal of Clinical Endocrinology and Metabolism. 81: 4479-83. PMID 8954063 DOI: 10.1210/jcem.81.12.8954063  0.36
1996 Kazmi MA, Dubin RA, Oddoux C, Ostrer H. High-level inducible expression of visual pigments in transfected cells Biotechniques. 21: 304-311. PMID 8862817  0.36
1996 Oddoux C, Struewing JP, Clayton CM, Neuhausen S, Brody LC, Kaback M, Haas B, Norton L, Borgen P, Jhanwar S, Goldgar D, Ostrer H, Offit K. The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1% Nature Genetics. 14: 188-190. PMID 8841192 DOI: 10.1038/ng1096-188  0.36
1996 Monteiro J, Batliwalla F, Ostrer H, Gregersen PK. Shortened telomeres in clonally expanded CD28-CD8+ T cells imply a replicative history that is distinct from their CD28+CD8+ counterparts Journal of Immunology. 156: 3587-3590. PMID 8621891  0.36
1995 Dubin RA, Coward P, Lau YFC, Ostrer H. Functional comparison of the Mus musculus molossinus and Mus musculus domesticus Sry genes Molecular Endocrinology. 9: 1645-1654. PMID 8614401  0.36
1995 Dubin RA, Kazmi MA, Ostrer H. Inverted repeats are necessary for circularization of the mouse testis Sry transcript Gene. 167: 245-248. PMID 8566785 DOI: 10.1016/0378-1119(95)00639-7  0.36
1995 Oddoux C, Reich E, Axelrod F, Blumenfeld A, Maayan C, Slaugenhaupt S, Gusella J, Ostrer H. Prenatal diagnostic testing for familial dysautonomia using linked genetic markers Prenatal Diagnosis. 15: 817-826. PMID 8559751 DOI: 10.1002/pd.1970150905  0.36
1995 Kronn D, Oddoux C, Phillips J, Ostrer H. Prevalence of canavan disease heterozygotes in the New York metropolitan Ashkenazi Jewish population [4] American Journal of Human Genetics. 57: 1250-1252. PMID 7485179  0.36
1994 Allen BS, Ostrer H. Conservation of human Y chromosome sequences among male great apes: implications for the evolution of Y chromosomes. Journal of Molecular Evolution. 39: 13-21. PMID 8064869 DOI: 10.1007/BF00178245  0.36
1994 Dubin RA, Ostrer H. Sry is a transcriptional activator Molecular Endocrinology. 8: 1182-1192. PMID 7838151 DOI: 10.1210/me.8.9.1182  0.36
1993 Ostrer H, Allen W, Crandall LA, Moseley RE, Dewar MA, Nye D, McCrary SV. Insurance and genetic testing: where are we now? American Journal of Human Genetics. 52: 565-77. PMID 8447322  0.36
1993 Ostrer H, Allen W. Equal employment opportunities commission issues new interim enforcement guidance on Americans with Disabilities Act [9] American Journal of Human Genetics. 53: 541-542. PMID 8328472  0.36
1993 Allen W, Ostrer H. Invited editorial: Anticipating unfair uses of genetic information American Journal of Human Genetics. 53: 16-21. PMID 8317481  0.36
1993 McCrary SV, Allen B, Moseley R, Crandall LA, Ostrer H, Curry RW, Dewar MA, Nye D. Ethical and practical implications of the human genome initiative for family medicine. Archives of Family Medicine. 2: 1158-63. PMID 8124491 DOI: 10.1001/archfami.1993.01850120082017  0.36
1992 Dewar MA, Moseley R, Ostrer H, Crandall L, Nye D, Allen B. Genetic screening by insurance carriers. Jama. 267: 1207-8. PMID 1538556 DOI: 10.1001/jama.1992.03480090055021  0.36
1991 Moseley R, Crandall L, Dewar M, Nye D, Ostrer H. Ethical implications of a complete human gene map for insurance. Business & Professional Ethics Journal. 10: 69-82. PMID 11659392  0.36
1991 Allen BS, Stein JL, Stein GS, Ostrer H. Single-copy flanking sequences in human histone gene clusters map to chromosomes 1 and 6. Genomics. 10: 486-8. PMID 2071153 DOI: 10.1016/0888-7543(91)90337-E  0.36
1991 Whisenant EC, Rasheed BKA, Ostrer H, Bhatnagar YM. Evolution and sequence analysis of a human Y-chromosomal DNA fragment Journal of Molecular Evolution. 33: 133-141. PMID 1920449 DOI: 10.1007/BF02193627  0.36
1991 Rasheed BKA, Whisenant EC, Fernandez R, Ostrer H, Bhatnagar YM. A Y-chromosomal DNA fragment is conserved in human and chimpanzee Molecular Biology and Evolution. 8: 416-432. PMID 1840631  0.36
1991 Morris N, Riconda D, Marfatia L, Ostrer H. Maternal serum alphafetoprotein screening. University Medical Center Journal of the Florida Medical Association. 78: 365-368. PMID 1714937  0.36
1990 Cantú ES, Ostrer H, Gray BA, Jackson LG, Williams CA. Establishment of a cytogenetic service for chorionic villus samples: the split specimen approach. Prenatal Diagnosis. 10: 137-9. PMID 2343025 DOI: 10.1002/pd.1970100215  0.36
1990 Williams CA, Zori RT, Stone JW, Gray BA, Cantu ES, Ostrer H. Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting. American Journal of Medical Genetics. 35: 350-3. PMID 2309781 DOI: 10.1002/ajmg.1320350308  0.36
1990 Matteson KJ, Barker PE, Kaplan GC, Mueller OT, Ostrer H, Phillips JA, Schwartz C. Regional evaluation of DNA diagnostic laboratories American Journal of Human Genetics. 46: 182-183. PMID 2294749  0.36
1990 Ostrer H. R.C. Philips Research and Education Unit Journal of the Florida Medical Association. 77: 829-831. PMID 2230706  0.36
1990 Zori RT, Schatz DA, Ostrer H, Williams CA, Spillar R, Riley WJ. Relationship of autoimmunity to thyroid dysfunction in children and adults with Down syndrome American Journal of Medical Genetics. 238-241. PMID 2149955  0.36
1989 Ostrer H, Clayton CM. Y chromosome mosaicism in 45,X Turner syndrome American Journal of Medical Genetics - Seminars in Medical Genetics. 34: 294-296. PMID 2817013  0.36
1989 Ostrer H, Wright G, Clayton M, Skordis N, MacGillivray MH. Familial XX chromosomal maleness does not arise from a Y chromosomal translocation The Journal of Pediatrics. 114: 977-982. PMID 2723912 DOI: 10.1016/S0022-3476(89)80441-X  0.36
1989 Ostrer H. Prenatal diagnosis of genetic disorders by DNA analysis Pediatric Annals. 18: 701-713. PMID 2573032  0.36
1989 Allen BS, Ketcham CM, Roberts RM, Nick HS, Ostrer H. Localization of the human type 5, tartrate-resistant acid phosphatase gene by in situ hybridization. Genomics. 4: 597-600. PMID 2473026 DOI: 10.1016/0888-7543(89)90284-X  0.36
1988 Ostrer H, Switzer B. Thoughts on hemochromatosis Journal of the Florida Medical Association. 75: 726. PMID 3204356  0.36
1988 Cantu ES, Marsh RD, Boecklen KE, Ostrer H. Selective protection of specific DNA sequences in the heterochromatin of C-banded human Y chromosomes American Journal of Human Genetics. 43: 948-953. PMID 3195592  0.36
1988 Ostrer H, Hejtmancik JF. Prenatal diagnosis and carrier detection of genetic diseases by analysis of deoxyribonucleic acid The Journal of Pediatrics. 112: 679-687. PMID 2896232 DOI: 10.1016/S0022-3476(88)80682-6  0.36
1987 Ostrer H, Henderson AL, Stringer LC. Characterization of Y chromosomal deoxyribonucleic acid fragments and translocations by Southern blot analysis. The Journal of Pediatrics. 111: 678-83. PMID 3312551 DOI: 10.1016/S0022-3476(87)80242-1  0.36
1986 Green L, Whittle W, Dell'Orco R, Ostrer H, Stein G, Stein J. Human histone gene organization. Identification of a histone gene polymorphism prevalent in a black population Experimental Cell Research. 164: 507-515. PMID 3011475 DOI: 10.1016/0014-4827(86)90048-0  0.36
1985 Hejtmancik JF, Beebe DC, Ostrer H, Piatigorsky J. δ- and β-crystallin mRNA levels in the embryonic and posthatched chicken lens: Temporal and spatial changes during development Developmental Biology. 109: 72-81. PMID 3987967 DOI: 10.1016/0012-1606(85)90347-1  0.36
1985 Matteson KJ, Ostrer H, Chakravarti A, Buetow KH, O'Brien WE, Beaudet AL, Phillips JA. A study of restriction fragment length polymorphisms at the human alpha-1-antitrypsin locus Human Genetics. 69: 263-267. PMID 2984106 DOI: 10.1007/BF00293037  0.36
1984 Ostrer H, Stamberg J, Perinchief P. Two chromosome aberrations in the child of a woman with systemic lupus erythematosus treated with azathioprine and prednisone American Journal of Medical Genetics. 17: 627-632. PMID 6711614  0.36
1984 Boyer SH, Ostrer H, Smith KD, Young KE, Noyes AN. Isolation of cDNA clones for rabbit red cell carbonic anhydrase and catalase: a pilot study directed at isolation of coordinately expressed genes. Annals of the New York Academy of Sciences. 429: 324-31. PMID 6204570  0.36
1982 Orkin SH, Kazazian HH, Antonarakis SE, Ostrer H, Goff SC, Sexton JP. Abnormal RNA processing due to the exon mutation of beta E-globin gene. Nature. 300: 768-9. PMID 7177196 DOI: 10.1038/300768a0  0.36
1982 Antonarakis SE, Orkin SH, Kazazian HH, Goff SC, Boehm CD, Waber PG, Sexton JP, Ostrer H, Fairbanks VF, Chakravarti A. Evidence for multiple origins of the beta E-globin gene in Southeast Asia. Proceedings of the National Academy of Sciences of the United States of America. 79: 6608-11. PMID 6292908 DOI: 10.1073/pnas.79.21.6608  0.36
1981 Ostrer H, Beebe DC, Piatigorsky J. β-crystallin mRNAs: Differential distribution in the developing chicken lens Developmental Biology. 86: 403-408. PMID 6169569 DOI: 10.1016/0012-1606(81)90198-6  0.36
1980 Ostrer H, Piatigorsky J. β-Crystallins of the adult chicken lens: Relatedness of the polypeptides and their aggregates Experimental Eye Research. 30: 679-689. PMID 7418745 DOI: 10.1016/0014-4835(80)90066-4  0.36
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