C. Oddoux

发表

Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry.

Itsik Pe'er, Gil Atzmon, Pier Francesco Palamara, 2010, American journal of human genetics.

North African Jewish and non-Jewish populations form distinctive, orthogonal clusters

David Comas, Itsik Pe'er, Gil Atzmon, 2012, Proceedings of the National Academy of Sciences.

The genetic history of Cochin Jews from India

Yedael Y. Waldman, H. Ostrer, E. Halperin, 2016, Human Genetics.

Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC

H. Ostrer, K. Kinzler, B. Vogelstein, 1997, Nature Genetics.

Expanded genetic screening panel for the Ashkenazi Jewish population

Judy H. Cho, H. Ostrer, I. Pe’er, 2015, Genetics in Medicine.

Mendelian diseases among Roman Jews: implications for the origins of disease alleles.

H. Ostrer, K. Nafa, L. Luzzatto, 1999, The Journal of clinical endocrinology and metabolism.

TβR-I(6A) Is a Candidate Tumor Susceptibility Allele

H. Ostrer, P. Vineis, J. Satagopan, 1999 .

Advances in Brief T b RI ( 6 A ) Is a Candidate Tumor Susceptibility Allele 1

H. Ostrer, P. Vineis, J. Satagopan, 1999 .

Novel mutations of epidermal growth factor receptor in localized prostate cancer.

M. Pincus, W. Gerald, J. Satagopan, 2006, Frontiers in bioscience : a journal and virtual library.

A novel variant in CDKN1C is associated with intrauterine growth restriction, short stature, and early-adulthood-onset diabetes.

Michael H. Guo, H. Ostrer, Yiping Shen, 2014, The Journal of clinical endocrinology and metabolism.

Characterization of a chicken hepatoma cell line with a specific defect in fibrinogen secretion

C. Oddoux, G. Grieninger, 1994, Hepatology.

KLF6 loss of function in human prostate cancer progression is implicated in resistance to androgen deprivation.

P. Unger, J. Melamed, C. Oddoux, 2012, The American journal of pathology.

Identification of the first non‐Jewish mutation in familial Dysautonomia

J. Gusella, M. Leyne, J. Mull, 2003, American journal of medical genetics. Part A.

Mendelian diseases among Roman Jews: implications for the origins of disease alleles.

H. Ostrer, K. Nafa, L. Luzzatto, 1999, The Journal of clinical endocrinology and metabolism.

High-Yield Noninvasive Human Genomic DNA Isolation Method for Genetic Studies

C. Oddoux, D. Kronn, J. Phillips, 2007 .

Assembly and secretion of fibrinogen. Degradation of individual chains.

S. Yu, C. Oddoux, C. Redman, 1992, The Journal of biological chemistry.

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.

C. Oddoux, J. Sun, W. G. Campbell, 1994, Circulation research.

Fibrinogen assembly: Insights from chicken hepatocytes

C. Oddoux, G. Grieninger, 1994, Hepatology.

The frequency of GJB2 and GJB6 mutations in the New York State newborn population: feasibility of genetic screening for hearing defects

H. Ostrer, R. Ruben, C. Oddoux, 2004, Clinical genetics.

The genetic history of Cochin Jews from India

Yedael Y. Waldman, H. Ostrer, E. Halperin, 2016, Human Genetics.

The impact of Converso Jews on the genomes of modern Latin Americans

H. Ostrer, I. Pe’er, P. Palamara, 2011, Human Genetics.

Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes.

H. Ostrer, D. Goldstein, X. Estivill, 1998, American journal of human genetics.

Dating the Origin of the CCR 5D 32 AIDS-Resistance Allele by the Coalescence of Haplotypes

H. Ostrer, D. Goldstein, X. Estivill, 2007 .

Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness.

H. Ostrer, C. Berlin, B. Keats, 1998, The New England journal of medicine.

Hearing Loss in Turner Syndrome

N. Sculerati, C. Oddoux, C. Clayton, 1996, The Laryngoscope.

SRY gene expression in the ovotestes of XX true hermaphrodites.

H. Ostrer, H. Yee, K. McElreavey, 2002, The Journal of urology.

Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination.

H. Ostrer, A. Sinclair, G. Camerino, 2010, American journal of human genetics.

Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function

H. Ostrer, B. Keats, S. Riazuddin, 2002, Nature Genetics.

The Genetics of Bene Israel from India Reveals Both Substantial Jewish and Indian Ancestry

Yedael Y. Waldman, H. Ostrer, E. Halperin, 2015, bioRxiv.

Characterization of the chicken apolipoprotein A-I gene 5'-flanking region.

C. Oddoux, D. Banerjee, N. Bhattacharyya, 1993, DNA and cell biology.

A mutation of PCDH15 among Ashkenazi Jews with the type 1 Usher syndrome.

Karen B Avraham, Harry Ostrer, Carole Oddoux, 2003, The New England journal of medicine.

Testing for Breast Cancer Risk in the Ashkenazim

H. Ostrer, C. Oddoux, E. Reich, 1999 .

The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%

Kenneth Offit, Jeffery P. Struewing, Lawrence C. Brody, 1996, Nature Genetics.

Copy number and gene expression differences between African American and Caucasian American prostate cancer

W. Gerald, A. Olshen, J. Satagopan, 2010, Journal of Translational Medicine.

No major association between TGFBR1*6A and prostate cancer

H. Ostrer, K. Offit, B. Pasche, 2004, BMC Genetics.

TbetaR-I(6A) is a candidate tumor susceptibility allele.

H. Ostrer, P. Vineis, J. Satagopan, 1999, Cancer research.

MDM2 expression and regulation in prostate cancer racial disparity.

W. Gerald, M. Mazumdar, I. Osman, 2009, International journal of clinical and experimental pathology.

Evaluation of the Utility of Interphase Cytogenetics to Detect Residual Cells with a Malignant Genotype in Mixed Cell Populations : A Burkitt Lymphoma Model

R. Glanville, C. Maslen, J. Mcmurtry, 2011 .

Polymorphisms of ADIPOQ and ADIPOR1 and prostate cancer risk.

Nengjun Yi, Kui Zhang, Kenneth Offit, 2011, Metabolism: clinical and experimental.

Prostate cancer susceptibility genes on 8p21–23 in a Dutch population

H. Ostrer, R. Goldbohm, M. Zeegers, 2013, Prostate Cancer and Prostatic Diseases.

Carboxy-terminal-extended variant of the human fibrinogen alpha subunit: a novel exon conferring marked homology to beta and gamma subunits.

Y. Fu, C. Oddoux, L. Weissbach, 1992, Biochemistry.

Assessing risk for Mendelian disorders in a Bronx population

H. Ostrer, C. Oddoux, K. Upadhyay, 2017, Molecular genetics & genomic medicine.

Combined genetic assessment of transforming growth factor-beta signaling pathway variants may predict breast cancer risk.

Junjian Liu, Kenneth Offit, Virginia G Kaklamani, 2005, Cancer research.

The impact of Converso Jews on the genomes of modern Latin

H. Ostrer, M. Hammer, P. Palamara, 2012 .

Variants of the adiponectin and adiponectin receptor 1 genes and breast cancer risk.

H. Ostrer, C. Mantzoros, K. Offit, 2008, Cancer research.

Rare variants of ATM and risk for Hodgkin's disease and radiation-associated breast cancers.

J. Satagopan, K. Offit, S. Jhanwar, 2002, Clinical cancer research : an official journal of the American Association for Cancer Research.

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.

H. Ostrer, D. Kastner, M. Pras, 1999, American journal of human genetics.

Genetic marker polymorphisms on chromosome 8q24 and prostate cancer in the Dutch population: DG8S737 may not be the causative variant

H. Ostrer, M. Zeegers, Humera S. Khan, 2011, European Journal of Human Genetics.

High-Level Inducible Expression of Visual Pigments in Transfected Cells

H. Ostrer, C. Oddoux, R. Dubin, 1999 .

The beta chain of chicken fibrinogen contains an atypical thrombin cleavage site.

C. Oddoux, L. Weissbach, R. Procyk, 1991, Biochemistry.

Prevalence of Bloom syndrome heterozygotes among Ashkenazi Jews.

H Ostrer, H. Ostrer, C. Oddoux, 1999, American journal of human genetics.

Renin gene promoter activity in GC cells is regulated by cAMP and thyroid hormone through Pit-1-dependent mechanisms.

C. Oddoux, J. Sun, W. Tansey, 1994, Journal of Biological Chemistry.

Prevalence of Canavan disease heterozygotes in the New York metropolitan Ashkenazi Jewish population.

H. Ostrer, C. Oddoux, D. Kronn, 1995, American journal of human genetics.

Severe factor XI deficiency in an Arab family associated with a novel mutation in exon 11

H. Ostrer, C. Oddoux, M. Nardi, 1997, British journal of haematology.

Promoter activity of human renin 5'-flanking DNA sequences is activated by the pituitary-specific transcription factor Pit-1.

C. Oddoux, J. Sun, A. Lazarus, 1993, The Journal of biological chemistry.

Prenatal diagnostic testing for familial dysautonomia using linked genetic markers

H. Ostrer, S. Slaugenhaupt, C. Oddoux, 1995, Prenatal diagnosis.

Expanded genetic screening panel for the Ashkenazi Jewish population

H. Ostrer, I. Pe’er, T. Lencz, 2015, Genetics in Medicine.

The Genetics of Bene Israel from India Reveals Both Substantial Jewish and Indian Ancestry

Yedael Y. Waldman, H. Ostrer, E. Halperin, 2015, bioRxiv.

North African Jewish and non-Jewish populations form distinctive, orthogonal clusters

H. Ostrer, C. Bustamante, I. Pe’er, 2012, Proceedings of the National Academy of Sciences.

Regulation of Fibrinogen Synthesis and Secretion by the Chicken Hepatocyte a

L. Diamond, C. Oddoux, L. Weissbach, 1989, Annals of the New York Academy of Sciences.

High-level inducible expression of visual pigments in transfected cells.

C. Oddoux, M. Kazmi, Harry Ostrer, 1996, BioTechniques.