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Carole Oddoux, Ph.D.

Publications

Publications

1. Wang, Guimin; Firoz, Elnaz F; Rose, Amy; Blochin, Elen; Christos, Paul; Pollens, Danuta; Mazumdar, Madhu; Gerald, William; Oddoux, Carole; Lee, Peng; Osman, Iman. "MDM2 Expression and Regulation in Prostate Cancer Racial Disparity". International journal of clinical & experimental pathology. 2009; 2: 353 (#J0157868)
2. 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)
3. Douglas, D; Zhong, H; Ro, J; Oddoux, C; Pincus, M; Satagopan, J; Gerald, W; Schei, H; Lee, P; Osman, I. "Novel mutations in tyrosine kinase domain of epidermal growth factor receptor in prostate cancer [Abstract]". Journal of clinical oncology. 2006; 24: 244S (#J0121895)
4. Douglas DA; Zhong H; Ro JY; Oddoux C; Berger AD; Pincus MR; Satagopan JM; Gerald WL; Scher HI; Lee P; Osman I. "Novel mutations of epidermal growth factor receptor in localized prostate cancer". Frontiers in biosciences. 2006; 11: 2518 (#J0114690)
5. 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)
6. 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)
7. 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)
8. 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)
9. Leyne M; Mull J; Gill SP; Cuajungco MP; Oddoux C; Blumenfeld A; Maayan C; Gusella JF; Axelrod FB; Slaugenhaupt SA. "Identification of the first non-Jewish mutation in familial Dysautonomia". American journal of medical genetics. 2003; 118A: 305 (#J0047946)
10. Oddoux, C; Maayan, C; Cilio, R; Axelrod, F. "Genotype-phenotype correlation of hereditary sensory neuropathy type 4: Extension of the phenotype [Abstract]". American journal of human genetics. 2003; 73: 550 (#J0101773)
11. 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)
12. Offit K; Gilad S; Paglin S; Kolachana P; Roisman LC; Nafa K; Yeugelewitz V; Gonzales M; Robson M; McDermott D; Pierce HH; Kauff ND; Einat P; Jhanwar S; Satagopan JM; Oddoux C; Ellis N; Skaliter R; Yahalom J. "Rare variants of ATM and risk for Hodgkin's disease and radiation-associated breast cancers". Clinical cancer research. 2002; 8: 3813 (#J0047947)
13. 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)
14. 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)
15. 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)
16. Oddoux, C; Ruben, RJ; Ostrer, H. "Perilymphatic fistulae associated with DFNB1-related hearing loss [Abstract]". American journal of human genetics. 2001; 69: 426 (#J0099064)
17. 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)
18. 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)
19. 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)
20. 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)
21. 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)
22. 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)
23. 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)
24. 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)
25. 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)
26. 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)
27. 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)
28. 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)
29. Kazmi MA; Dubin RA; Oddoux C; Ostrer H. "High-level inducible expression of visual pigments in transfected cells". Biotechniques. 1996; 21: 304 (#J0010293)
30. 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)
31. Sculerati N; Oddoux C; Clayton CM; Lim JW; Oster H. "Hearing loss in Turner syndrome". Laryngoscope. 1996; 106: 992 (#J0010309)
32. 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)
33. 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)
34. 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)
35. Gilbert MT; Sun J; Yan Y; Oddoux C; Lazarus A; Tansey WP; Lavin TN; Catanzaro DF. "Renin gene promoter activity in GC cells is regulated by cAMP and thyroid hormone through Pit-1-dependent mechanisms". Journal of biological chemistry. 1994; 269: 28049 (#J0047953)
36. Oddoux C; Grieninger G. "Characterization of a chicken hepatoma cell line with a specific defect in fibrinogen secretion". Hepatology. 1994; 19: 682 (#J0047956)
37. Oddoux C; Grieninger G. "Fibrinogen assembly: insights from chicken hepatocytes". Hepatology. 1994; 19: 688 (#J0047955)
38. Sun J; Oddoux C; Gilbert MT; Yan Y; Lazarus A; Campbell WG Jr; Catanzaro DF. "Pituitary-specific transcription factor (Pit-1) binding site in the human renin gene 5'-flanking DNA stimulates promoter activity in placental cell primary cultures and pituitary lactosomatotropic cell lines". Circulation research. 1994; 75: 624 (#J0047954)
39. Bhattacharyya N; Chattapadhyay R; Oddoux C; Banerjee D. "Characterization of the chicken apolipoprotein A-I gene 5'-flanking region". DNA & cell biology. 1993; 12: 597 (#J0047957)
40. Sun J; Oddoux C; Lazarus A; Gilbert MT; Catanzaro DF. "Promoter activity of human renin 5'-flanking DNA sequences is activated by the pituitary-specific transcription factor Pit-1". Journal of biological chemistry. 1993; 268: 1505 (#J0047958)
41. Fu Y; Weissbach L; Plant PW; Oddoux C; Cao Y; Liang TJ; Roy SN; Redman CM; Grieninger G. "Carboxy-terminal-extended variant of the human fibrinogen alpha subunit: a novel exon conferring marked homology to beta and gamma subunits". Biochemistry. 1992; 31: 11968 (#J0047959)
42. Roy S; Yu S; Banerjee D; Overton O; Mukhopadhyay G; Oddoux C; Grieninger G; Redman C. "Assembly and secretion of fibrinogen. Degradation of individual chains". Journal of biological chemistry. 1992; 267: 23151 (#J0047960)
43. Weissbach L; Oddoux C; Procyk R; Grieninger G. "The beta chain of chicken fibrinogen contains an atypical thrombin cleavage site". Biochemistry. 1991; 30: 3290 (#J0047961)
44. Grieninger G; Oddoux C; Diamond L; Weissbach L; Plant PW. "Regulation of fibrinogen synthesis and secretion by the chicken hepatocyte". Annals of the New York Academy of Sciences. 1989; 557: 257 (#J0047962)

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