Harry Ostrer
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Harry Ostrer's Degrees
- Doctorate Medicine Albert Einstein College of Medicine
- PhD Genetics Columbia University
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(Suggest an Edit or Addition)Harry Ostrer's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC (1997) (686)
- Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness. (1998) (559)
- The case against perfection Ethics in the age of genetic engineering (2007) (526)
- Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (2018) (509)
- Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes. (1998) (490)
- Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function (2002) (406)
- Shortened telomeres in clonally expanded CD28-CD8+ T cells imply a replicative history that is distinct from their CD28+CD8+ counterparts. (1996) (401)
- The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1% (1996) (383)
- Genome-wide patterns of population structure and admixture among Hispanic/Latino populations (2010) (329)
- 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. (1999) (306)
- Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes. (2000) (270)
- SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development (2000) (268)
- Abnormal RNA processing due to the exon mutation of βE-globin gene (1982) (262)
- Empiric risk of prostate carcinoma for relatives of patients with prostate carcinoma (2003) (245)
- The History of African Gene Flow into Southern Europeans, Levantines, and Jews (2011) (239)
- Functional variants in the LRRK2 gene confer shared effects on risk for Crohn’s disease and Parkinson’s disease (2018) (233)
- DREAM4: Combining Genetic and Dynamic Information to Identify Biological Networks and Dynamical Models (2010) (228)
- Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry. (2010) (212)
- A genetic profile of contemporary Jewish populations (2001) (187)
- Gene flow from North Africa contributes to differential human genetic diversity in southern Europe (2013) (179)
- Expression of steroidogenic factor 1 and Wilms' tumour 1 during early human gonadal development and sex determination (1999) (179)
- PCAdmix: Principal Components-Based Assignment of Ancestry Along Each Chromosome in Individuals with Admixed Ancestry from Two or More Populations (2012) (163)
- Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction (2021) (163)
- Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination. (2010) (161)
- TβR-I(6A) Is a Candidate Tumor Susceptibility Allele (1999) (158)
- A Genome-Wide Scan of Ashkenazi Jewish Crohn's Disease Suggests Novel Susceptibility Loci (2012) (148)
- Loss of Mitogen-Activated Protein Kinase Kinase Kinase 4 (MAP3K4) Reveals a Requirement for MAPK Signalling in Mouse Sex Determination (2009) (146)
- Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins (2014) (146)
- 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. (2010) (144)
- How strong is the association between CAG and GGN repeat length polymorphisms in the androgen receptor gene and prostate cancer risk? (2004) (143)
- Inverted repeats are necessary for circularization of the mouse testis Sry transcript. (1995) (137)
- Sry is a transcriptional activator. (1994) (131)
- Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting. (1990) (126)
- Variants of the adiponectin and adiponectin receptor 1 genes and breast cancer risk. (2008) (112)
- Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotype (1997) (104)
- Radiogenomics: using genetics to identify cancer patients at risk for development of adverse effects following radiotherapy. (2014) (98)
- Radiogenomics: radiobiology enters the era of big data and team science. (2014) (96)
- Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations (2004) (96)
- Individual patient data meta-analysis shows a significant association between the ATM rs1801516 SNP and toxicity after radiotherapy in 5456 breast and prostate cancer patients. (2016) (92)
- Evidence for multiple origins of the beta E-globin gene in Southeast Asia. (1982) (91)
- Disorders of sex development (DSDs): an update. (2014) (91)
- A mutation of PCDH15 among Ashkenazi Jews with the type 1 Usher syndrome. (2003) (89)
- Genetic variants in SOD2, MPO, and NQO1, and risk of ovarian cancer. (2004) (89)
- Association of Single Nucleotide Polymorphisms in SOD2, XRCC1 and XRCC3 with Susceptibility for the Development of Adverse Effects Resulting from Radiotherapy for Prostate Cancer (2008) (89)
- Dating the Origin of the CCR 5D 32 AIDS-Resistance Allele by the Coalescence of Haplotypes (2007) (88)
- The population genetics of the Jewish people (2012) (84)
- Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants (2018) (83)
- Mutations in MAP3K1 tilt the balance from SOX9/FGF9 to WNT/β-catenin signaling. (2014) (82)
- Combined genetic assessment of transforming growth factor-beta signaling pathway variants may predict breast cancer risk. (2005) (82)
- TbetaR-I(6A) is a candidate tumor susceptibility allele. (1999) (82)
- Familial Sex Reversal: A Review (2000) (81)
- Abnormal RNA processing due to the exon mutation of beta E-globin gene. (1982) (80)
- Founder mutations among the Dutch (2004) (75)
- δ- and β-crystallin mRNA levels in the embryonic and posthatched chicken lens: Temporal and spatial changes during development (1985) (74)
- A versatile statistical analysis algorithm to detect genome copy number variation. (2004) (69)
- TGFB1 single nucleotide polymorphisms are associated with adverse quality of life in prostate cancer patients treated with radiotherapy. (2008) (67)
- A 2-stage genome-wide association study to identify single nucleotide polymorphisms associated with development of erectile dysfunction following radiation therapy for prostate cancer. (2013) (65)
- The Troubled Dream of Genetic Medicine: Ethnicity and Innovation in Tay-Sachs, Cystic Fibrosis, and Sickle Cell Disease (2006) (65)
- STROGAR – STrengthening the Reporting Of Genetic Association studies in Radiogenomics (2013) (65)
- Minor Abnormalities of Testis Development in Mice Lacking the Gene Encoding the MAPK Signalling Component, MAP3K1 (2011) (64)
- 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. (1998) (63)
- Polymorphisms of ADIPOQ and ADIPOR1 and prostate cancer risk. (2011) (63)
- Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate Cancer (2016) (63)
- Integrative genomics identifies molecular alterations that challenge the linear model of melanoma progression. (2011) (62)
- Clinical review 111: familial sex reversal: a review. (2000) (61)
- Radiogenomics Consortium Genome-Wide Association Study Meta-Analysis of Late Toxicity After Prostate Cancer Radiotherapy (2019) (60)
- Relationship of autoimmunity to thyroid dysfunction in children and adults with Down syndrome. (2005) (58)
- Increased Resolution of Y Chromosome Haplogroup T Defines Relationships among Populations of the Near East, Europe, and Africa (2011) (56)
- Mutation of a conserved cysteine in the X-linked cone opsins causes color vision deficiencies by disrupting protein folding and stability. (1997) (55)
- A 2-stage genome-wide association study to identify single nucleotide polymorphisms associated with development of urinary symptoms after radiotherapy for prostate cancer. (2013) (55)
- Insurance and genetic testing: where are we now? (1993) (55)
- A Cellular Study of Human Testis Development (2007) (54)
- Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity. (2004) (54)
- Prevalence of Canavan disease heterozygotes in the New York metropolitan Ashkenazi Jewish population. (1995) (52)
- IMMUNOLOCALIZATION OF ANDROGEN RECEPTOR AND ESTROGEN RECEPTORS α AND β IN HUMAN FETAL TESTIS AND EPIDIDYMIS (2005) (52)
- Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes. (2014) (50)
- Machine Learning on a Genome-wide Association Study to Predict Late Genitourinary Toxicity After Prostate Radiation Therapy. (2018) (49)
- The Prediction of Radiotherapy Toxicity Using Single Nucleotide Polymorphism-Based Models: A Step Toward Prevention. (2015) (48)
- Cancer Risk Assessment Using Genetic Panel Testing: Considerations for Clinical Application (2014) (47)
- Genome-wide association study identifies a region on chromosome 11q14.3 associated with late rectal bleeding following radiation therapy for prostate cancer. (2013) (47)
- Genetic marker polymorphisms on chromosome 8q24 and prostate cancer in the Dutch population: DG8S737 may not be the causative variant (2011) (45)
- Association of MDM2 SNP309, Age of Onset, and Gender in Cutaneous Melanoma (2009) (45)
- North African Jewish and non-Jewish populations form distinctive, orthogonal clusters (2012) (45)
- Will the new cytogenetics replace the old cytogenetics? (2004) (45)
- Association for Molecular Pathology v. Myriad Genetics, Inc. (2013) (44)
- A novel variant in CDKN1C is associated with intrauterine growth restriction, short stature, and early-adulthood-onset diabetes. (2014) (44)
- The inferelator 2.0: A scalable framework for reconstruction of dynamic regulatory network models (2009) (43)
- Genome-wide association of single-nucleotide polymorphisms with weight loss outcomes after Roux-en-Y gastric bypass surgery. (2013) (43)
- A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalance. (2008) (43)
- Developing a multidisciplinary prospective melanoma biospecimen repository to advance translational research. (2009) (43)
- beta-Crystallins of the adult chicken lens: relatedness of the polypeptides and their aggregates. (1980) (40)
- The genetics of mitral valve prolapse (2007) (40)
- The impact of Converso Jews on the genomes of modern Latin Americans (2012) (38)
- Beta-crystallin mRNAs: differential distribution in the developing chicken lens. (1981) (38)
- De novo 12;17 translocation upstream of SOX9 resulting in 46,XX testicular disorder of sex development (2010) (35)
- Tumor suppressor function of androgen receptor coactivator ARA70alpha in prostate cancer. (2010) (34)
- MAP3K1‐related gonadal dysgenesis: Six new cases and review of the literature (2017) (32)
- Computational methods using genome-wide association studies to predict radiotherapy complications and to identify correlative molecular processes (2017) (32)
- Expanded genetic screening panel for the Ashkenazi Jewish population (2015) (31)
- Genome-Wide Association Study Identifies a Region on Chromosome 11q14.3 Associated With Late Rectal Bleeding Following Radiation Therapy for Prostate Cancer (2013) (31)
- SRY gene expression in the ovotestes of XX true hermaphrodites. (2002) (30)
- Two chromosome aberrations in the child of a woman with systemic lupus erythematosus treated with azathioprine and prednisone. (1984) (29)
- Invited review: sex-based differences in gene expression. (2001) (29)
- The frequency of GJB2 and GJB6 mutations in the New York State newborn population: feasibility of genetic screening for hearing defects (2004) (27)
- Human embryo and early fetus research (2006) (26)
- How Will Big Data Improve Clinical and Basic Research in Radiation Therapy? (2016) (26)
- Y chromosome mosaicism in 45,X Turner syndrome. (1989) (24)
- Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation (2013) (24)
- Immunolocalization of androgen receptor and estrogen receptors alpha and beta in human fetal testis and epididymis. (2005) (23)
- Single-copy flanking sequences in human histone gene clusters map to chromosomes 1 and 6. (1991) (21)
- 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. (2013) (21)
- Mapping a gene for 46,XY gonadal dysgenesis by linkage analysis (2003) (20)
- Prevalence of Bloom syndrome heterozygotes among Ashkenazi Jews. (1999) (20)
- Functional comparison of the Mus musculus molossinus and Mus musculus domesticus Sry genes. (1995) (20)
- Consumers’ Desire towards Current and Prospective Reproductive Genetic Testing (2009) (20)
- Sex-based differences in gene transmission and gene expression (1999) (20)
- Radiation biology and oncology in the genomic era. (2018) (20)
- Severe factor XI deficiency in an Arab family associated with a novel mutation in exon 11 (1997) (19)
- Prenatal diagnosis and carrier detection of genetic diseases by analysis of deoxyribonucleic acid. (1988) (18)
- Mutations in MAP3K1 that cause 46,XY disorders of sex development disrupt distinct structural domains in the protein. (2019) (18)
- No major association between TGFBR1*6A and prostate cancer (2004) (17)
- Rapidly screening variants of uncertain significance in the MAP3K1 gene for phenotypic effects (2012) (17)
- Mendelian diseases among Roman Jews: implications for the origins of disease alleles. (1999) (17)
- Legacy: A Genetic History of the Jewish People (2012) (16)
- Genetic counseling for prostate cancer risk (2003) (16)
- High-depth whole genome sequencing of an Ashkenazi Jewish reference panel: enhancing sensitivity, accuracy, and imputation (2018) (16)
- The Genetics of Bene Israel from India Reveals Both Substantial Jewish and Indian Ancestry (2015) (15)
- Sex determination: lessons from families and embryos (2001) (14)
- Functional variant analyses (FVAs) predict pathogenicity in the BRCA1 DNA double-strand break repair pathway. (2015) (14)
- Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility (2022) (13)
- Familial XX chromosomal maleness does not arise from a Y chromosomal translocation. (1989) (13)
- Anticipating unfair uses of genetic information. (1993) (13)
- Missense mutation in the MEN1 gene discovered through whole exome sequencing co-segregates with familial hyperparathyroidism. (2013) (12)
- Frequencies of obesity susceptibility alleles among ethnically and racially diverse bariatric patient populations. (2013) (12)
- Novel ultra-rare exonic variants identified in a founder population implicate cadherins in schizophrenia (2020) (11)
- Predicting response to TNF antagonists in rheumatoid arthritis: the promise of pharmacogenetics research using clinical registries. (2007) (11)
- Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (2019) (11)
- Robinow syndrome with developmental brain dysplasia. (1997) (11)
- High-level inducible expression of visual pigments in transfected cells. (1996) (11)
- Changing the game with whole exome sequencing (2011) (11)
- Characterization of Y chromosomal deoxyribonucleic acid fragments and translocations by Southern blot analysis. (1987) (10)
- Glycosylation and palmitoylation are not required for the formation of the X-linked cone opsin visual pigments. (1998) (10)
- Spastic paraplegia, optic atrophy, microcephaly with normal intelligence, and XY sex reversal: a new autosomal recessive syndrome? (1998) (10)
- Prenatal diagnostic testing for familial dysautonomia using linked genetic markers (1995) (9)
- Ethical implications of a complete human gene map for insurance. (1991) (9)
- A study of restriction fragment length polymorphisms at the human alpha-1-antitrypsin locus (1985) (9)
- Translating genomic research into clinical practice: promise and pitfalls. (2013) (9)
- Alterations of sex differentiation in males: from candidate genes to diagnosis and treatments. (2004) (9)
- The genetic history of Cochin Jews from India (2016) (9)
- Essentials of Medical Genomics (2002) (8)
- A Y-chromosomal DNA fragment is conserved in human and chimpanzee. (1991) (8)
- Robust genomic copy number predictor of pan cancer metastasis (2018) (8)
- Ectopic Otoconin 90 expression in triple negative breast cancer cell lines is associated with metastasis functions (2019) (8)
- Identifying genes for male sex determination in humans. (2001) (8)
- Sequencing of over 100,000 individuals identifies multiple genes and rare variants associated with Crohns disease susceptibility (2021) (8)
- Prostate cancer susceptibility genes on 8p21–23 in a Dutch population (2013) (7)
- Sexual differentiation. (2000) (7)
- Non-Mendelian Genetics in Humans (1998) (7)
- Intrauterine and postnatal growth failure with normal GH/IGF1 axis and insulin-resistant diabetes in a consanguineous kinship. (2012) (7)
- Linkage analysis of a kindred with inherited 46,XY partial gonadal dysgenesis. (1996) (6)
- Localization of the human type 5, tartrate-resistant acid phosphatase gene by in situ hybridization. (1989) (6)
- Ethical and practical implications of the human genome initiative for family medicine. (1993) (6)
- Biallelic mutations in FLNB cause a skeletal dysplasia with 46,XY gonadal dysgenesis by activating β‐catenin (2018) (5)
- delta- and beta-Crystallin mRNA levels in the embryonic and posthatched chicken lens: temporal and spatial changes during development. (1985) (5)
- Mutation of a conserved proline disrupts the retinal-binding pocket of the X-linked cone opsins. (1997) (5)
- The origin of the p.E180 growth hormone receptor gene mutation. (2016) (5)
- Prediction of breast cancer risk based on flow-variant analysis of circulating peripheral blood B cells (2017) (5)
- Differential analysis of mutations in the Jewish population and their implications for diseases (2017) (5)
- Benefits and dangers of genetic tests (1998) (5)
- Equal Employment Opportunities Commission issues new interim enforcement guidance on Americans with Disabilities Act. (1993) (5)
- Acro-renal-ocular syndrome: expansion of the phenotype. (1998) (5)
- Regional evaluation of DNA diagnostic laboratories. (1990) (4)
- Genetic screening by insurance carriers. (1992) (4)
- Evolution and sequence analysis of a human Y-chromosomal DNA fragment (1991) (4)
- Clustering-Based Method for Developing a Genomic Copy Number Alteration Signature for Predicting the Metastatic Potential of Prostate Cancer. (2012) (4)
- Glioma-like proliferation within tissues excised as tubers in patients with tuberous sclerosis complex (2008) (4)
- Genome-wide data from medieval German Jews show that the Ashkenazi founder event pre-dated the 14th century (2022) (4)
- Advances in Brief T b RI ( 6 A ) Is a Candidate Tumor Susceptibility Allele 1 (1999) (3)
- Genome Wide Association Study to Identify Single Nucleotide Polymorphisms (SNPs) Associated with the Development of Erectile Dysfunction in African-American Men Following Radiotherapy for Prostate Cancer (2010) (3)
- Human histone gene organization. Identification of a histone gene polymorphism prevalent in a black population. (1986) (3)
- Erratum: Combined genetic assessment of transforming growth factor-β signaling pathway variants may predict breast cancer risk (Cancer Research (April 15, 2005) 65 (3454-3461)) (2006) (3)
- Three synchronous primary carcinomas in a patient with HNPCC associated with a novel germline mutation in MLH1: Case report (2009) (3)
- Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction (2021) (3)
- Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (2019) (3)
- A genetic view of Jewish history (2008) (3)
- THE ASSOCIATION FOR MOLECULAR PATHOLOGY, THE AMERICAN COLLEGE OF MEDICAL GENETICS, THE AMERICAN SOCIETY FOR CLINICAL PATHOLOGY, THE COLLEGE OF AMERICAN PATHOLOGISTS, HAIG KAZAZIAN, MD, (2010) (3)
- Association of MDM 2 SNP 309 , Age of Onset , and Gender in CutaneousMelanoma (2009) (2)
- Rapid Next-Generation Sequencing Method for Prediction of Prostate Cancer Risks. (2019) (2)
- Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction (2021) (2)
- Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes (2014) (2)
- Identifying novel high-impact rare disease-causing mutations, genes and pathways in exomes of Ashkenazi Jewish inflammatory bowel disease patients (2020) (2)
- X-Inactivation and Cytogenetic Studies in a Family with Sensorineural Hearing Loss and Turner Syndrome (1995) (2)
- Cancer Risk C (CR-C), a functional genomics test is a sensitive and rapid test for germline mismatch repair deficiency. (2022) (2)
- GENETC SCREENING BY INSURANCE CARRIERS. AUTHOR'S REPLY (1992) (2)
- biallelic haplotypes Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome (2000) (2)
- Genes in the polyamine biosynthesis pathway may be involved in prostate cancer susceptibility. (2005) (2)
- Selective protection of specific DNA sequences in the heterochromatin of C-banded human Y chromosomes. (1988) (1)
- OC-0082: A machine learning method demonstrates that a large number of SNPs contribute to clinical radiosensitivity (2015) (1)
- Isoation of cDNA Clones for Rabbit Red Cell Carbonic Anhydrase and Catalase: A Pilot Study Directed at Isolation of Coordinately Expressed Genes (1984) (1)
- Genome-wide Association Study to Identify Genetic Variants Associated With the Development of Erectile Dysfunction Following Radiation Therapy for Prostate Cancer (2012) (1)
- Health care professionals’ attitudes toward cancer gene panel testing (2021) (1)
- Bioinformatics in otolaryngology research. Part two: other high-throughput platforms in genomics and epigenetics (2014) (1)
- Cerebral myelin deficiency in teenage girls with the 18q- syndrome (1994) (1)
- High-depth whole genome sequencing of a large population-specific reference panel: Enhancing sensitivity, accuracy, and imputation (2017) (1)
- Pathogenic Variants in MAP3K1 Cause 46,XY Gonadal Dysgenesis: A Review (2022) (1)
- Genetic Predictors of Cervical Dysplasia in African American HIV-Infected Women: ACTG DACS 268 (2013) (1)
- Genes: US patent rulings will fuel invention (2013) (1)
- Break Repair Pathway (2015) (1)
- Prediction of breast cancer risk based on flow variant analysis of circulating peripheral blood mononuclear cells (2022) (1)
- Conservation of human Y chromosome sequences among male great apes: Implications for the evolution of Y chromosomes (1994) (1)
- Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants (2018) (1)
- X-Inactivation and Cytogenetic Studies in a Family with Sensorineural Hearing Loss and Turner Syndrome (1995) (1)
- The murine Sry gene encodes a nuclear transcriptional activator (1994) (1)
- Bioinformatics in otolaryngology research. Part one: concepts in DNA sequencing and gene expression analysis (2014) (1)
- Embryo: A defense of human life (2008) (1)
- Identification of tyrosinase polymorphisms for use in melanoma risk assessment. (2010) (1)
- Abstract OT1-11-01: Phase II study of talazoparib, a PARP inhibitor, in somatic BRCA1/2 mutant metastatic breast cancer identified by cell-free DNA or tumor tissue genotyping (2023) (0)
- Acknowledgement to the Reviewers (2006) (0)
- Breast Cancer Genetics And The Sephardic Jewish Woman (2008) (0)
- Testing for Breast Cancer Risk in the Ashkenazim (1999) (0)
- The genetic history of Cochin Jews from India (2016) (0)
- PARENTS' ATTITUDES TOWARD PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS AND PHENYLKETONURIA (1987) (0)
- Genetics of Sexual Differentiation (2009) (0)
- Thoughts on hemochromatosis. (1988) (0)
- PV-0564: Predicting Genitourinary Toxicity by Machine Learning on Genome-Wide Single Nucleotide Polymorphisms (2018) (0)
- Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (2018) (0)
- Chapter 20 – Genetic Counseling for Patients with Breast Cancer and Their Families (2005) (0)
- SU-D-204-06: Integration of Machine Learning and Bioinformatics Methods to Analyze Genome-Wide Association Study Data for Rectal Bleeding and Erectile Dysfunction Following Radiotherapy in Prostate Cancer. (2016) (0)
- Diagnostic Heteroduplexes: Simple Detection of Carriers of a 4-bp Insertion Mutation in Tay-Sachs Disease (2006) (0)
- Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation (2013) (0)
- Non- mendelian genetics in harpy (2013) (0)
- Insurance andGenetic Testing: WhereAreWe Now? (1993) (0)
- Survey of Radiation Oncologists to Assess Interest and Potential Use of a Genetic Test Predicting Susceptibility for the Development of Toxicities After Prostate Cancer Radiation Therapy (2020) (0)
- The impact of Converso Jews on the genomes of modern Latin Americans (2011) (0)
- Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (2019) (0)
- Identification of Single Nucleotide Polymorphisms (SNPs) Associated With Late Toxicity Following Radiation Therapy for Prostate Cancer Through a Meta-Analysis of Genome-Wide Association Studies (GWAS) (2014) (0)
- Male Sex Determination: Genetics (2006) (0)
- Tumorigenesis and Neoplastic Progression Tumor Suppressor Function of Androgen Receptor Coactivator ARA 70 in Prostate Cancer (2010) (0)
- Recruitment in the Internet era: An efficient strategy for a study of breast cancer risk. (2011) (0)
- Stuart Brown with John Hay and Harry Ostrer (2004) (0)
- Abstract OT2-24-03: Phase II study of a PARP inhibitor in metastatic breast cancer with somaticBRCA1/2mutations identified by cell-free DNA: Genotyping based clinical trial (2022) (0)
- The use of integrative genomics to define molecular signatures of melanoma histologic subtypes. (2010) (0)
- EFFICIENT DETECTION OF Y CHROMOSOMAL DELETIONS, TRANSLOCATIONS AND MOSAICISM USING CHROMOSOME-SPECIFIC DNA PROBES (1987) (0)
- Diaspora, migration, and the sciences: a new integrated perspective (2018) (0)
- Maternal serum alphafetoprotein screening. University Medical Center. (1991) (0)
- Immunocytochemical Localization of Synaptonemal Complex Proteins in Mouse Oocytes (2000) (0)
- OC-0081: Prediction of normal tissue radiosensitivity from random numbers??? Be cautious out there! (2010) (0)
- Impact of population genetic substructure on association studies and risk assessment for melanoma. (2011) (0)
- A novel multi-SNP model predictive of erectile dysfunction following radiotherapy in prostate cancer (2016) (0)
- High-depth whole genome sequencing of an Ashkenazi Jewish reference panel: enhancing sensitivity, accuracy, and imputation (2018) (0)
- OP-JNCI190078 1..12 (2019) (0)
- Book Review Jacob's Legacy: A Genetic View of Jewish History By David B. Goldstein. 148 pp. New Haven, CT, Yale University Press, 2008. $26. 978-0-300-12583-2 (2008) (0)
- Genomic Basis of Prostate Cancer Health Disparity Among African-American Men (2014) (0)
- Genome-Wide Association Study to Identify SNPs and CNPs Associated with Development of Radiation Injury in Prostate Cancer Patients Treated with Radiotherapy (2011) (0)
- 344 GENETIC FACTORS INFLUENCE TIME TO UNDETECTABLE PSA IN MEN WITH PROSTATE CANCER TREATED BY RADIOTHERAPY (2011) (0)
- Comprar Essentials of Medical Genomics | Hiroyuki Osada | 9780470140192 | Wiley (2009) (0)
- Association of Genetic Factors With PSA Response in Prostate Cancer Patients Receiving Definitive Radiation Therapy (2012) (0)
- Genome Wide Association Study to Identify Genetic Variants Associated With Urinary Symptoms Following Radiation Therapy for Prostate Cancer (2012) (0)
- Response to Zlotogora and Meiner (2015) (0)
- Genetic Testing for the Practitioner (2008) (0)
- ATM rs1801516 SNP and toxicity after radiotherapy (2017) (0)
- Contribution of Common SNPs to Variability in Late Radiation Therapy Toxicity in Prostate Cancer (2017) (0)
- EPITHELIAL AND STROMAL MICRORNA EXPRESSION IN RACIAL DISPARITY OF PROSTATE CANCER (2009) (0)
- Individual patient data meta-analysis shows a significant association between the ATM rs1801516 SNP and toxicity after radiotherapy in 5,456 breast and prostate cancer patients (2017) (0)
- Diaspora, migration, and the sciences: a new integrated perspective (2018) (0)
- Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction (2021) (0)
- EP-2058: A novel multi-SNP model predictive of erectile dysfunction following radiotherapy in prostate cancer (2016) (0)
- The unique molecular signatures of nodular and superficial spreading melanoma. (2009) (0)
- Evidence for multiple origins of the fiE-globin gene in Southeast Asia ( DNA polymorphisms / haplotypes / population genetics / hemoglobinopathies ) (2003) (0)
- Establishment of a cytogenetic service for chorionic villus samples: The split specimen approach (1990) (0)
- Genetic Modeling of Radiation Injury in Prostate Cancer Patients Treated with Radiotherapy (2016) (0)
- Germline variation at 8q24 and prostate cancer risk in men of European ancestry (2018) (0)
- The population genetics of the Jewish people (2012) (0)
- BRIEF OF AMICI CURIAE, INFORMATION SOCIETY PROJECT AT YALE LAW SCHOOL SCHOLARS IN SUPPORT OF PLAINTIFFS-APPELLEES d (2010) (0)
- Developing genetic markers for melanoma risk assessment. (2009) (0)
- Genetic Susceptibility to Prostate Cancer in the Netherlands (2001) (0)
- EVIDENCE THAT CELL SURFACE HY ANTIGEN IS NOT THE SOLE MEDIATOR OF NORMAL HUMAN SPERMATOGENESIS (1987) (0)
- P-175 Pleiotropic Effects of Novel Functional LRRK2 Variation on Crohn's Disease and Parkinson's Disease Risk (2016) (0)
- Single-Nucleotide Polymorphisms (SNPs) Associated With Radiation Proctitis From Genome-wide False Discovery Rate Analysis (2012) (0)
- R.C. Philips Research and Education Unit. (1990) (0)
- GROWTH FAILURE: STATISTICS APPLIED TO MEDICAL THERAPY (1977) (0)
- Prenatal diagnosis of genetic disorders by DNA analysis. (1989) (0)
- Comprar Evidence at Hand | Stuart M. Brown | 9780470178911 | Wiley (2009) (0)
- AWARD NUMBER: W81XWH-12-1-0259 TITLE: Genomic Basis of Prostate Cancer Health Disparity Among African-American Men (2013) (0)
- Table of Contents, Volume 175C, Number 2, June 2017 (2017) (0)
- Preconditioned Random Forest Regression: Application to Genome-Wide Study for Radiotherapy Toxicity Prediction (2017) (0)
- Gene Patenting Panel (2014) (0)
- OC-0142: Radiogenomics consortium meta-analysis of genome wide association studies of prostate radiotherapy late toxicity (2014) (0)
- Meta-Analysis of Genome-Wide Association Studies (GWAS) of Late Toxicity in 3,874 Men Treated with Radiation for Prostate Cancer (2018) (0)
- Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients (2023) (0)
- Evaluation of the melanocortin-1-receptor gene in melanoma predisposition, progression, and recurrence. (2009) (0)
- Assessing risk for Mendelian disorders in a Bronx population (2017) (0)
- Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (2019) (0)
- Array comparative genomic hybridization analysis of heritable Xp deletion (2009) (0)
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What Schools Are Affiliated With Harry Ostrer?
Harry Ostrer is affiliated with the following schools:
