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Harry Ostrer, M.D.
Publications
| 1. | Bogani, D; Siggers, P; Brixey, R; Warr, N; Beddow, S; Edwards, J; Williams, D; Wilhelm, D; Koopman, P; Flavell, RA; Chi, HB; 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. 2009; 7: 7 (#J0180623) |
| 2. | Firoz, Elnaz F; Warycha, Melanie; Zakrzewski, Jan; Pollens, Danuta; Wang, Guimin; Shapiro, Richard; Berman, Russell; Pavlick, Anna; Manga, Prashiela; Ostrer, Harry; Celebi, Julide Tok; Kamino, Hideko; Darvishian, Farbod; Rolnitzky, Linda; Goldberg, Judith D; Osman, Iman; Polsky, David. "Association of MDM2 SNP309, age of onset, and gender in cutaneous melanoma". Clinical cancer research. 2009; 15: 2573 (#J0180616) |
| 3. | Hathaway, Feighanne; Burns, Esther; Ostrer, Harry. "Consumers' desire towards current and prospective reproductive genetic testing". Journal of genetic counseling. 2009; 18: 137 (#J0163667) |
| 4. | Manga P; Goldberg JD; Belitskaya-Levy I; Lobach I; Polsky D; Pavlick A; Shapiro R; Berman R; Osman I; Ostrer H. "Developing genetic markers for melanoma risk assessment [Abstract]". Journal of clinical oncology. 2009; 27: 15S (#J0176403) |
| 5. | Purushothaman, Radhika; Gunturu, Sreenivas Dutt; Anhalt, Henry; Ten, Svetlana; Friedman, Andrew; Pearlman, Alexander; Ostrer, Harry. "Array comparative genomic hybridization analysis of heritable Xp deletion". American journal of medical genetics. Pt A. 2009; 149A: 529 (#J0163666) |
| 6. | Sidash S; Ostrer H; Goldberg JD; Belitskaya-Levy I; Lobach I; Polsky D; Shapiro RL; Berman RS; Osman I; Manga P. "Evaluation of the melanocortin-1-receptor gene in melanoma predisposition, progression and recurrence [Abstract]". Journal of clinical oncology. 2009; 27: 15S (#J0176404) |
| 7. | Burri, Ryan J; Stock, Richard G; Cesaretti, Jamie A; Atencio, David P; Peters, Sheila; Peters, Christopher A; Fan, Grace; Stone, Nelson N; Ostrer, Harry; Rosenstein, Barry S. "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. 2008; 170: 49 (#J0163668) |
| 8. | 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. 2008; 116: 67 (#J0139067) |
| 9. | Gordon, Earl; Panaghie, Gianina; Deng, Liyong; Bee, Katharine J; Roepke, Torsten K; Krogh-Madsen, Trine; Christini, David J; Ostrer, Harry; Basson, Craig T; Chung, Wendy; Abbott, Geoffrey W. "A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalance". Cardiovascular research. 2008; 77: 98 (#J0163669) |
| 10. | Kaklamani, Virginia G; Sadim, Maureen; Hsi, Alex; Offit, Kenneth; Oddoux, Carole; Ostrer, Harry; Ahsan, Habibul; Pasche, Boris; Mantzoros, Christos. "Variants of the adiponectin and adiponectin receptor 1 genes and breast cancer risk". Cancer research. 2008; 68: 3178 (#J0163639) |
| 11. | Peters, Christopher A; Stock, Richard G; Cesaretti, Jamie A; Atencio, David P; Peters, Sheila; Burri, Ryan J; Stone, Nelson N; Ostrer, Harry; Rosenstein, Barry S. "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. 2008; 70: 752 (#J0163670) |
| 12. | Grau, J B; Pirelli, L; Yu, P-J; Galloway, A C; Ostrer, H. "The genetics of mitral valve prolapse". Clinical genetics. 2007; 72: 288 (#J0130999) |
| 13. | Greenberg, Jeffrey D; Ostrer, Harry. "Predicting response to TNF antagonists in rheumatoid arthritis: the promise of pharmacogenetics research using clinical registries". Bulletin of the NYU Hospital for Joint Diseases. 2007; 65: 139 (#J0129163) |
| 14. | Ostrer, H; Huang, H Y; Masch, R J; Shapiro, E. "A cellular study of human testis development". Sexual development : genetics, molecular biology, evolution, endocrinology, embryology and pathology of sex determination & differentiation. 2007; 1: 286 (#J0137554) |
| 15. | Bersson, Y; Pearlman, A; Shajahan, S; Ostrer, H; Oratz, R. "BRCA1 and BRCA2 mutations: 185delAG, 5382insC and 6174deIT; Ashkenazi founder or Jewish determinant? [Abstract]". Breast cancer research & treatment. 2006; 100: S180 (#J0124862) |
| 16. | Ostrer, H; Wilson, D I; Hanley, N A. "Human embryo and early fetus research". Clinical genetics. 2006; 70: 98 (#J0120771) |
| 17. | 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; Offit K; Pasche B. "Combined genetic assessment of transforming growth factor-beta signaling pathway variants may predict breast cancer risk". Cancer research. 2005; 65: 3454 (#J0109890) |
| 18. | 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". Journal of urology. 2005; 174: 1695 (#J0105590) |
| 19. | Zeegers, Maurice P; Ostrer, Harry. "Genes in the polyamine biosynthesis pathway may be involved in prostate cancer susceptibility". Future Oncology. 2005; 1: 683 (#J0163671) |
| 20. | 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. 2004; 114: 354 (#J0069696) |
| 21. | 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. 2004; 101: 16292 (#J0103293) |
| 22. | 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. 2004; 65: 338 (#J0069693) |
| 23. | 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; Malcolm S; Mendelsohn C; Preston RA; Retik AB; Schneck FX; Wright V; Ye XY; Woolf AS; Wu XR; Ostrer H; Shapiro E; Yu J; Sun TT. "Lack of major involvement of human uroplakin genes in vesicoureteral reflux: Implications for disease heterogeneity". Kidney international. 2004; 66: 10 (#J0067774) |
| 24. | 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. 2004; 5: 28 (#J0109892) |
| 25. | Olson SH; Carlson MD; Ostrer H; Harlap S; Stone A; Winters M; Ambrosone CB. "Genetic variants in SOD2, MPO, and NQO1, and risk of ovarian cancer". Gynecologic oncology. 2004; 93: 615 (#J0069761) |
| 26. | Ostrer H. "Alterations of sex differentiation in males: from candidate genes to diagnosis and treatments". Current pharmaceutical design. 2004; 10: 501 (#J0069695) |
| 27. | Salman M; Jhanwar S; Ostrer H. "Will the new cytogenetics replace the old cytogenetics?". Clinical genetics. 2004; 66: 265 (#J0069692) |
| 28. | Zeegers MP; van Poppel F; Vlietinck R; Spruijt L; Ostrer H. "Founder mutations among the Dutch". European journal of human genetics. 2004; 12: 591 (#J0069694) |
| 29. | Zeegers, Maurice P; Kiemeney, Lambertus A L M; Nieder, Alan M; Ostrer, Harry. "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. 2004; 13: 1765 (#J0163672) |
| 30. | 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". New England journal of medicine. 2003; 348: 1664 (#J0047945) |
| 31. | Brown, Stuart M; Hay, John G; Ostrer, Harry. "Essentials of medical genomics". Hoboken NJ : Wiley-Liss, 2003. 2003; xiv, 274 (#B0001310) |
| 32. | Jawaheer D; Juo SH; 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. 2003; 63: 530 (#J0069697) |
| 33. | Nieder AM; Taneja SS; Zeegers MP; Ostrer H. "Genetic counseling for prostate cancer risk". Clinical genetics. 2003; 63: 169 (#J0053293) |
| 34. | Ostrer, H; Fritsch, B; Giudice, T; Bing, R; Hillman, D; Beisel, K. "Expression of degenerin BNaC/ASIC isoforms in hair cells of the mammalian cochlea [Abstract]". American journal of human genetics. 2003; 73: 339 (#J0101770) |
| 35. | Zeegers MP; Jellema A; Ostrer H. "Empiric risk of prostate carcinoma for relatives of patients with prostate carcinoma: a meta-analysis". Cancer. 2003; 97: 1894 (#J0069698) |
| 36. | Zeegers, M; Vlietinck, R; van Poppel, F; Spruijt, L; Ostrer, H. "Founder mutations among the Dutch [Abstract]". American journal of human genetics. 2003; 73: 397 (#J0101772) |
| 37. | 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; Khan S; Riazuddin S; Deininger PL; Hampton LL; Sullivan SL; Battey JF Jr; Keats BJ; Wilcox ER; Friedman TB; Griffith AJ. "Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function". Nature genetics. 2002; 30: 277 (#J0047949) |
| 38. | Ortenberg J; Oddoux C; Craver R; McElreavey K; Salas-Cortes L; Guillen-Navarro E; Ostrer H; Sarafoglou K. "SRY gene expression in the ovotestes of XX true hermaphrodites". Journal of urology. 2002; 167: 1828 (#J0047948) |
| 39. | Caggana, M; Duva, S; Ostrer, H; Oddoux, C; Ruben, R; Pass, K. "An effective pooling strategy for feasible newborn screening of GBJ-2 gene mutations [Abstract]". American journal of human genetics. 2001; 69: 426 (#J0099063) |
| 40. | Khoja, H; Nagashima, J; Giannoukos, G; Leushner, J; Oddoux, C; Ostrer, H; McGinniss, M. "Design and development of an Ashkenazi Jewish mutation panel using MALDI-TOF mass spectrometer [Abstract]". Clinical chemistry. 2001; 47: 2082 (#J0099129) |
| 41. | Levy, B; Huang, M; McElreavey, K; Ostrer, H. "Analysis of genetic sex reversal by comparative genomic hybridization [Abstract]". American journal of human genetics. 2001; 69: 322 (#J0099060) |
| 42. | Oddoux, C; Ruben, RJ; Ostrer, H. "Perilymphatic fistulae associated with DFNB1-related hearing loss [Abstract]". American journal of human genetics. 2001; 69: 426 (#J0099064) |
| 43. | Ostrer H. "A genetic profile of contemporary Jewish populations". Nature reviews. Genetics. 2001; 2: 891 (#J0028812) |
| 44. | Ostrer, H; Jawaheer, D; Juo, SH; Petit, C; Damle, A; Dowbak, S; Gregersen, P; MeElreavey, K. "A gene for human testis determination maps to chromosome [Abstract]". American journal of human genetics. 2001; 69: 213 (#J0099056) |
| 45. | Ostrer H. "Identifying genes for male sex determination in humans". Journal of experimental zoology. 2001; 290: 567 (#J0028790) |
| 46. | Ostrer H. "Invited review: sex-based differences in gene expression". Journal of applied physiology (Bethesda). 2001; 91: 2384 (#J0028797) |
| 47. | Ostrer H. "Sex determination: lessons from families and embryos". Clinical genetics. 2001; 59: 207 (#J0022250) |
| 48. | 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. 2000; 97: 6769 (#J0022251) |
| 49. | Hanley NA; Hagan DM; Clement-Jones M; Ball SG; Strachan T; Salas-Cortes 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. 2000; 91: 403 (#J0022252) |
| 50. | Oddoux, C; Yee, H; Clarke, V; Clayton, CM; McElreavey, K; MacGillivray, M; Ostrer, H. "Paternally transmitted recurrent true-hermaphroditism associated with SRY mosaicism [Abstract]". American journal of human genetics. 2000; 67: 149 (#J0097496) |
| 51. | Ostrer H. "Sexual differentiation". Seminars in reproductive medicine. 2000; 18: 41 (#J0022249) |
| 52. | Sarafoglou K; Ostrer H. "Clinical review 111: familial sex reversal: a review". Journal of clinical endocrinology & metabolism. 2000; 85: 483 (#J0009121) |
| 53. | 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. 1999; 64: 949 (#J0022254) |
| 54. | Hammer, MF; Wood, ET; Redd, AJ; Bonner, MR; Karafet, T; Santachiara-Benerecetti, AS; Oppenheim, A; Jobling, M; Ostrer, H; Bonne-Tamir, B. "Origins and diversity of Jewish Y-chromosome haplotypes [Abstract]". American journal of human genetics. 1999; 65: A41 (#J0095504) |
| 55. | 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. 1999; 87: 175 (#J0022253) |
| 56. | Oddoux, C; Wang, J; Clayton, CM; Hilz, M; Cilio, R; Bertini, E; Mayaan, C; Blumenfeld, A; Axelrod, F; Ostrer, H. "Genetic heterogeneity in hereditary and autonomic sensory neuropathy type 4 (HSAN4) [Abstract]". American journal of human genetics. 1999; 65: A482 (#J0095518) |
| 57. | 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; Aksentijevich I; Kastner D; Axelrod F; Ostrer H . "Mendelian diseases among Roman Jews: implications for the origins of disease alleles". Journal of clinical endocrinology & metabolism. 1999; 84: 4405 (#J0004234) |
| 58. | Oddoux C; Clayton CM; Nelson HR; Ostrer H. "Prevalence of Bloom syndrome heterozygotes among Ashkenazi Jews [Letter]". American journal of human genetics. 1999; 64: 1241 (#J0047951) |
| 59. | Ostrer H. "Sex-based differences in gene transmission and gene expression". Lupus. 1999; 8: 365 (#J0104013) |
| 60. | 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; Massague J; Offit K. "TbetaR-I(6A) is a candidate tumor susceptibility allele". Cancer research. 1999; 59: 5678 (#J0047950) |
| 61. | Guillen-Navarro E; Wallerstein R; Reich E; Zajac L; Ostrer H. "Acro-renal-ocular syndrome: expansion of the phenotype". Clinical dysmorphology. 1998; 7: 243 (#J0104711) |
| 62. | 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. 1998; 158: 777 (#J0002917) |
| 63. | 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". New England journal of medicine. 1998; 339: 1500 (#J0104760) |
| 64. | Ostrer H. "Benefits and dangers of genetic tests [letter] [comment]". Nature. 1998; 392: 14 (#J0104773) |
| 65. | 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. 1998; 4: 28 (#J0104611) |
| 66. | Ostrer, Harry. "Non-mendelian genetics in humans". New York : Oxford University Press, 1998. 1998; x, 202 (#B0000933) |
| 67. | 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; Oddoux C; di Giovine FS; Nasioulas G; Chandler D; Aseev M; Hanson M; Kalaydjieva L; Glavac D; Gasparini P; Kanavakis E; Claustres M; Kambouris M; Ostrer H; Duff G; Baranov V; Sibul H; Metspalu A; Goldman D; Martin N; Duffy D; Schmidtke J; Estivill X; O'Brien SJ; Dean M. "Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes". American journal of human genetics. 1998; 62: 1507 (#J0104901) |
| 68. | 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. 1998; 35: 759 (#J0104818) |
| 69. | Guillen-Navarro, E; Chan, WC; Ragoussis, J; Davies, AF; Ostrer, H; Perle, MA. "A rare de novo microdeletion of distal chromosome 6p: clinical phenotype and molecular cytogenetic characterization [Abstract]". American journal of human genetics. 1997; 61: A127 (#J0094883) |
| 70. | Hanley, NA; Hagan, DM; Ostrer, H; Guillen-Navarro, E; Wilson, DI; Bullen, P; Lindsay, S; Robson, S; Clement-Jones, M; Strachan, T. "Spatiotemporal expression patterns of the sex determining genes, SRY, SOX9, & WT1, during early human development [Abstract]". American journal of human genetics. 1997; 61: A154 (#J0094884) |
| 71. | Jawaheer, D; McElreavey, K; Berkovitz, G; Braun, A; Gregersen, PK; Ostrer, H. "Mapping of testis determining genes by linkage analysis in families with sex reversal [Abstract]". American journal of human genetics. 1997; 61: A400 (#J0094899) |
| 72. | 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 & visual science. IOVS. 1997; 38: 1074 (#J0104506) |
| 73. | 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; Vogelstein B. "Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC". Nature genetics. 1997; 17: 79 (#J0047952) |
| 74. | Oddoux, C; Guillen-Navarro, E; Clayton, CM; Nelson, H; Peretz, H; Seligsohn, U; Luzzatto, L; Nardi, M; Karpatkin, M; DiTivoli, C; DiCave, E; Axelrod, F; Ostrer, H. "Genetic evidence for a common origin among Roman Jews and Ashkenazi Jews [Abstract]". American journal of human genetics. 1997; 61: A207 (#J0094888) |
| 75. | Ostrer, H; Kazmi, MA. "Genetic mechanisms of human color vision deficiencies [Abstract]". American journal of human genetics. 1997; 61: A342 (#J0094895) |
| 76. | Ostrer H; Kazmi MA. "Mutation of a conserved proline disrupts the retinal-binding pocket of the X-linked cone opsins". Molecular vision. 1997; 3: 16 (#J0009665) |
| 77. | 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 & neck surgery. 1997; 117: S221 (#J0004347) |
| 78. | 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. 1997; 99: 575 (#J0009755) |
| 79. | Cohen, Sandra; Gulik, Roy; Kieran, Owen; Klapper, Allan; Lockwood, Charles; Ostrer, Harry. "Highlights of Feb. 1996 - Mar. 1996 television placements [videorecording]". 1996. 1996; (#B0001124) |
| 80. | 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". Journal of clinical endocrinology & metabolism. 1996; 81: 4479 (#J0092112) |
| 81. | Kazmi MA; Dubin RA; Oddoux C; Ostrer H. "High-level inducible expression of visual pigments in transfected cells". Biotechniques. 1996; 21: 304 (#J0010293) |
| 82. | Monteiro, J; Batliwalla, F; Ostrer, H; Gregersen, P K. "Shortened telomeres in clonally expanded CD28-CD8+ T cells imply a replicative history that is distinct from their CD28+CD8+ counterparts". Journal of immunology. 1996; 156: 3587 (#J0159060) |
| 83. | 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. 1996; 14: 188 (#J0003577) |
| 84. | Young JG; Brasic JR; Ostrer H; Kaplan D, Will M; John ER; Princhep L; Buschsbaum M. "The developing brain and mind: advances in research techniques" IN: Child and adolescent psychiatry: a comprehensive textbook Baltimore : Williams & Wilkins, 1996. 1996; 1209 (#C0000196) |
| 85. | Dubin RA; Coward P; Lau YF; Ostrer H. "Functional comparison of the Mus musculus molossinus and Mus musculus domesticus Sry genes". Molecular endocrinology. 1995; 9: 1645 (#J0104356) |
| 86. | Dubin RA; Kazmi MA; Ostrer H. "Inverted repeats are necessary for circularization of the mouse testis Sry transcript". Gene. 1995; 167: 245 (#J0001636) |
| 87. | KRONN, D; ODDOUX, C; PHILLIPS, J; OSTRER, H. "PREVALENCE OF CANAVAN-DISEASE HETEROZYGOTES IN THE NEW-YORK METROPOLITAN ASHKENAZI POPULATION [Abstract]". American journal of human genetics. 1995; 57: 944 (#J0149034) |
| 88. | Kronn D; Oddoux C; Phillips J; Ostrer H. "Prevalence of Canavan disease heterozygotes in the New York metropolitan Ashkenazi Jewish population [letter]". American journal of human genetics. 1995; 57: 1250 (#J0104868) |
| 89. | 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. 1995; 15: 817 (#J0001546) |
| 90. | 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. 1994; 39: 13 (#J0091308) |
| 91. | ALLEN, BS; OSTRER, H. "MAPPING THE LONG ARM OF THE HUMAN Y-CHROMOSOME - CONSERVATION AMONG HIGHER PRIMATES [Abstract]". Cytogenetics & cell genetics. 1994; 67: 387 (#J0090855) |
| 92. | Dubin RA; Ostrer H. "Sry is a transcriptional activator". Molecular endocrinology. 1994; 8: 1182 (#J0104174) |
| 93. | Allen W; Ostrer H. "Anticipating unfair uses of genetic information [Comment]". American journal of human genetics. 1993; 53: 16 (#J0039692) |
| 94. | DUBIN, RA; OSTRER, H. "UNUSUAL SPLICING OF SRY TRANSCRIPTS IN ADULT-MOUSE TESTES [Abstract]". American journal of human genetics. 1993; 53: 640 (#J0090468) |
| 95. | OSTRER, H; ALLEN, W. "EQUAL-EMPLOYMENT OPPORTUNITIES COMMISSION ISSUES NEW INTERIM ENFORCEMENT GUIDANCE ON AMERICANS-WITH-DISABILITIES-ACT". American journal of human genetics. 1993; 53: 541 (#J0090606) |
| 96. | Ostrer H; Allen W; Crandall LA; Moseley RE; Dewar MA; Nye D; McCrary SV. "Insurance and genetic testing: where are we now? [see comments]". American journal of human genetics. 1993; 52: 565 (#J0011469) |
| 97. | ZACKOWSKI, JL; CANTU, ES; DRISCOLL, DJ; OSTRER, H; ZORI, RT; GRAY, BA; PHILIPS, RC. "X-INACTIVATION PATTERNS IN MULTIPLE TISSUES OF 3 CASES OF APPARENTLY BALANCED X/AUTOSOME TRANSLOCATIONS WITH ABNORMAL PHENOTYPES [Abstract]". Cytogenetics & cell genetics. 1992; 60: 264 (#J0089440) |
| 98. | CHEN, H; WONG, R; MIRKIN, D; URBAN, M; NANAGAS, V; CULLEY, L; OSTRER, H; BEHZADIAN, A; THO, S; MCDONOUGH, P. "CLINICAL AND CYTOGENETIC SPECTRUM AND Y-PROBE STUDIES IN PATIENTS WITH 45 X/46,X,MAR(Y) MOSAICISM [Abstract]". Pediatric research. 1991; 29: A128 (#J0088626) |
| 99. | OSTRER, H; CLAYTON, CM; HUIE, MA; MACGILLIVRAY, MH. "FURTHER EVIDENCE FOR AN AUTOSOMAL MECHANISM FOR MULTIPLE OCCURRENCES OF XX-MALENESS AND XX TRUE HERMAPHRODITISM WITHIN A FAMILY [Abstract]". Pediatric research. 1991; 29: A133 (#J0088627) |
| 100. | OSTRER, H; ALLEN, BS. "MAPPING THE EUCHROMATIC LONG ARM OF THE HUMAN Y-CHROMOSOME - DEVELOPMENT OF LANDMARK PROBES AND A STANDARD PANEL OF CELL-LINES [Abstract]". Cytogenetics & cell genetics. 1991; 58: 2095 (#J0090013) |
| 101. | OSTRER, H; CLAYTON, CM; HUIE, MA; MACGILLIVRAY, MH. "XX-MALENESS AND XX-TRUE HERMAPHRODITISM - A SEX-LIMITED AUTOSOMAL DOMINANT TRAIT WITH VARIABLE EXPRESSION [Abstract]". American journal of human genetics. 1991; 49: 396 (#J0088056) |
| 102. | Schowalter, John E; Young, J. Gerald; Brasic, James R; Kaplan, Diana; Golomb, James; Ostrer, Harry; Furman, Jasmin; Biegon, Anat; Levine, Robert J. "Training and research" IN: Child and adolescent psychiatry: A comprehensive textbook Baltimore, MD : Williams & Wilkins Co., 1991. 1991; 1197 (#C0000159) |
| 103. | Young JG; Brasic JR; Kaplan D; Golomb J; Ostrer H; Furman J; Biegon A. "Advances in research techniques" IN: Child and adolescent psychiatry: a comprehensive textbook Baltimore : Williams & Wilkins, 1991. 1991; 1201 (#C0000195) |
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