Mary-Claire King

Q: What Schools Are Affiliated With Mary-Claire King

Mary-Claire King is affiliated with the following schools: University of California, Berkeley, Carleton College, Portland State University, University of Costa Rica, University of Washington, University of California, San Francisco

Mary-Claire King's AcademicInfluence.com Rankings

Mary-Claire King

Biology

#557

World Rank

#984

Historical Rank

#314

USA Rank

Genetics

#61

World Rank

#93

Historical Rank

#40

USA Rank

biology Degrees

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Biology

Mary-Claire King's Degrees

PhD Genetics University of California, Berkeley

Why Is Mary-Claire King Influential?

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According to Wikipedia, Mary-Claire King is an American geneticist. She was the first to show that breast cancer can be inherited due to mutations in the gene she called BRCA1. She studies human genetics and is particularly interested in genetic heterogeneity and complex traits. She studies the interaction of genetics and environmental influences and their effects on human conditions such as breast and ovarian cancer, inherited deafness, schizophrenia, HIV, systemic lupus erythematosus and rheumatoid arthritis. She has been the American Cancer Society Professor of the Department of Genome Sciences and of Medical Genetics in the Department of Medicine at the University of Washington since 1995.

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Mary-Claire King'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

Strong Association of De Novo Copy Number Mutations with Autism (2007) (2746)
Evolution at two levels in humans and chimpanzees. (1975) (2684)
Linkage of early-onset familial breast cancer to chromosome 17q21. (1990) (2525)
Initial sequence of the chimpanzee genome and comparison with the human genome (2005) (2222)
Breast and Ovarian Cancer Risks Due to Inherited Mutations in BRCA1 and BRCA2 (2003) (1810)
Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia (2008) (1764)
Atherogenic lipoprotein phenotype. A proposed genetic marker for coronary heart disease risk. (1990) (1426)
Genetic Heterogeneity in Human Disease (2010) (972)
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing (2011) (850)
Tamoxifen and breast cancer incidence among women with inherited mutations in BRCA1 and BRCA2: National Surgical Adjuvant Breast and Bowel Project (NSABP-P1) Breast Cancer Prevention Trial. (2001) (751)
Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas (2013) (740)
Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer. (2006) (706)
Microduplications of 16p11.2 are Associated with Schizophrenia (2009) (685)
Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families (1994) (664)
BRCA1 and BRCA2 and the genetics of breast and ovarian cancer. (2001) (631)
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. (2008) (578)
A recurrent 16p12.1 microdeletion suggests a two-hit model for severe developmental delay (2010) (561)
Population genetics of BRCA1 and BRCA2. (1997) (554)
Inherited Mutations in Women With Ovarian Carcinoma. (2016) (544)
Host Genotype-Specific Therapies Can Optimize the Inflammatory Response to Mycobacterial Infections (2012) (515)
Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy. (2014) (514)
Inheritance of human breast cancer: evidence for autosomal dominant transmission in high-risk families. (1988) (502)
Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network (2013) (487)
Ten genes for inherited breast cancer. (2007) (483)
The lta4h Locus Modulates Susceptibility to Mycobacterial Infection in Zebrafish and Humans (2010) (482)
Structure of a BRCA1–BARD1 heterodimeric RING–RING complex (2001) (473)
Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing (2010) (469)
Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous. (1997) (412)
Frequency of breast cancer attributable to BRCA1 in a population-based series of American women. (1998) (396)
Growth retardation and tumour inhibition by BRCA1 (1996) (393)
Concordance for Type 2 (non-insulin-dependent) diabetes mellitus in male twins (1987) (382)
Breast-cancer risk in families with mutations in PALB2. (2014) (367)
Insights into the functions of BRCA1 and BRCA2. (2000) (344)
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans. (1998) (334)
Enabling the genomic revolution in Africa (2014) (327)
Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study. (1998) (316)
Schizophrenia: a common disease caused by multiple rare alleles (2007) (313)
Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis. (1997) (290)
Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1. (1996) (288)
Population-based screening for breast and ovarian cancer risk due to BRCA1 and BRCA2 (2014) (288)
Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy (2015) (284)
Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82. (2010) (279)
Social structuring of mammalian populations and rate of chromosomal evolution. (1975) (277)
BRCA1 transcriptionally regulates genes involved in breast tumorigenesis (2002) (268)
A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia (2013) (253)
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13) (1999) (249)
Inherited breast and ovarian cancer. What are the risks? What are the choices? (1993) (247)
Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens. (2014) (247)
Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer. (2011) (246)
Closing in on a breast cancer gene on chromosome 17q. (1992) (245)
Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome. (2010) (241)
Identification of Id4 as a regulator of BRCA1 expression by using a ribozyme-library-based inverse genomics approach. (2001) (240)
Genome-wide scan for familial nasopharyngeal carcinoma reveals evidence of linkage to chromosome 4 (2002) (239)
Inherited breast and ovarian cancer. (1995) (237)
Population-based screening for BRCA1 and BRCA2: 2014 Lasker Award. (2014) (232)
From flies' eyes to our ears: Mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30 (2002) (231)
Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome (2011) (230)
Identifying individuals by sequencing mitochondrial DNA from teeth (1992) (228)
Risk factors for coronary heart disease in adult female twins. Genetic heritability and shared environmental influences. (1987) (220)
Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia (2011) (219)
Mutation analysis of the BRCA1 gene in ovarian cancers. (1995) (215)
Inheritance of low-density lipoprotein subclass patterns: results of complex segregation analysis. (1988) (215)
BRCA1 is secreted and exhibits properties of a granin (1996) (207)
Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185delAG in Ashkenazi Jewish families. (1995) (206)
A PROPOSED GENETIC MARKER FOR CORONARY HEART DISEASE RISK (1990) (202)
ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing. (2012) (201)
Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families (2011) (195)
BRCA2 in American families with four or more cases of breast or ovarian cancer: recurrent and novel mutations, variable expression, penetrance, and the possibility of families whose cancer is not attributable to BRCA1 or BRCA2. (1997) (189)
Accurate and exact CNV identification from targeted high-throughput sequence data (2011) (184)
Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered protease. (2013) (182)
Occupational Segregation by Race and Sex, 1940-88. (1992) (181)
The gene for an inherited form of deafness maps to chromosome 5q31. (1992) (177)
Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study. (1996) (177)
Mutations in LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome. (2013) (174)
Familial male breast cancer is not linked to the BRCA1 locus on chromosome 17q (1994) (173)
The Future of Psychiatric Research: Genomes and Neural Circuits (2010) (171)
Call for a worldwide survey of human genetic diversity: a vanishing opportunity for the Human Genome Project. (1991) (167)
Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1. (2001) (161)
Mapping the Functional Domains of BRCA1 (1999) (160)
Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation in the VRK1 gene. (2009) (152)
Duplications of the Neuropeptide Receptor VIPR2 Confer Significant Risk for Schizophrenia (2011) (151)
Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies. (2016) (150)
Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study. (1986) (148)
Genetic Information and the Workplace: Legislative Approaches and Policy Challenges (1997) (146)
DBC2, a candidate for a tumor suppressor gene involved in breast cancer. (2002) (146)
Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East (2002) (144)
Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden. (1996) (142)
Male influences on cervical cancer risk. (1986) (142)
PRACTICAL GUIDE FOR ESTIMATING RISK FOR FAMILIAL BREAST CANCER (1983) (140)
Mutations in Homologous Recombination Genes and Outcomes in Ovarian Carcinoma Patients in GOG 218: An NRG Oncology/Gynecologic Oncology Group Study (2017) (140)
BRCA1 RING Domain Cancer-predisposing Mutations (2001) (136)
MASP1 mutations in patients with facial, umbilical, coccygeal, and auditory findings of Carnevale, Malpuech, OSA, and Michels syndromes. (2010) (134)
Mutation of the ATP-gated P2X2 receptor leads to progressive hearing loss and increased susceptibility to noise (2013) (133)
The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population. (2002) (129)
Genetic variation among the Mapuche Indians from the Patagonian region of Argentina: mitochondrial DNA sequence variation and allele frequencies of several nuclear genes. (1993) (128)
Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population. (2005) (123)
Inherited mutations in cancer susceptibility genes are common among survivors of breast cancer who develop therapy‐related leukemia (2016) (123)
The Complexities and Potential of Theorizing Gender, Caste, Race, and Class (2002) (119)
Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease (2014) (119)
Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss. (2006) (116)
Familial breast cancer in a population-based series. (1986) (115)
Functional Characterization of a Novel BRCA1-Null Ovarian Cancer Cell Line in Response to Ionizing Radiation (2007) (112)
Reduced transcript expression of genes affected by inherited and de novo CNVs in autism (2011) (108)
Possible linkage of the estrogen receptor gene to breast cancer in a family with late-onset disease. (1991) (108)
Tumor-specific p53 sequences in blood and peritoneal fluid of women with epithelial ovarian cancer. (2005) (107)
Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity (2015) (107)
BRCA1, TP53, and CHEK2 germline mutations in uterine serous carcinoma (2013) (104)
Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients (2016) (101)
Prevalence of founder BRCA1 and BRCA2 mutations among breast and ovarian cancer patients in Hungary (2000) (101)
Comparative analysis of cancer genes in the human and chimpanzee genomes (2006) (99)
Inherited predisposition to breast cancer among African American women (2014) (96)
Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51. (2010) (96)
Familial clustering of site-specific cancer risks associated with BRCA1 and BRCA2 mutations in the Ashkenazi Jewish population. (2006) (96)
Inherited predisposition to breast and ovarian cancer. (1994) (94)
DBC2, a candidate for a tumor suppressor gene involved in breast cancer (2002) (91)
The Cancer-predisposing Mutation C61G Disrupts Homodimer Formation in the NH2-terminal BRCA1 RING Finger Domain* (1998) (90)
Human, canine and murine BRCA1 genes: sequence comparison among species. (1996) (89)
Search For: (2006) (89)
Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families (2010) (87)
Detecting linkage for genetically heterogeneous diseases and detecting heterogeneity with linkage data. (1986) (87)
Albumin Differences Among Ranid Frogs: Taxonomic and Phylogenetic Implications (1973) (87)
Risk of breast cancer to relatives of young breast cancer patients. (1985) (86)
High-density genetic map of the BRCA1 region of chromosome 17q12-q21. (1993) (86)
The influence of social and political violence on the risk of pregnancy complications. (1992) (86)
Inherited predisposition to malignant mesothelioma and overall survival following platinum chemotherapy (2019) (85)
THRA1 and D17S183 flank an interval of < 4 cM for the breast-ovarian cancer gene (BRCA1) on chromosome 17q21. (1993) (84)
Mutations in Twinkle primase-helicase cause Perrault syndrome with neurologic features (2014) (78)
Mutant ADA2 in vasculopathies. (2014) (78)
Improving performance of multigene panels for genomic analysis of cancer predisposition (2016) (76)
Genetic interrelationship between insulin-dependent diabetes mellitus, the autoimmune thyroid diseases, and rheumatoid arthritis. (1986) (76)
Maternal famine, de novo mutations, and schizophrenia. (2006) (76)
Spectrum of Mutations in BRCA 1 , BRCA 2 , CHEK 2 , and TP 53 in Families at High Risk of Breast Cancer (2006) (75)
Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy (2013) (75)
Race: A genetic melting-pot (2003) (73)
“The Race” to Clone BRCA1 (2014) (73)
Tumor necrosis factor a microsatellite polymorphism is associated with rheumatoid arthritis severity through an interaction with the HLA-DRB1 shared epitope. (1999) (71)
A phase I trial of retroviral BRCA1sv gene therapy in ovarian cancer. (1997) (71)
Inherited Breast Cancer in Nigerian Women (2018) (70)
Response to DNA damage of CHEK2 missense mutations in familial breast cancer. (2012) (68)
Genomic analysis of mental illness: a changing landscape. (2010) (68)
Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome. (2011) (65)
Genetics of schizophrenia in the South African Xhosa (2020) (63)
Incidence of BRCA1 and BRCA2 mutations in 54 Chilean families with breast/ovarian cancer, genotype–phenotype correlations (2005) (62)
Evidence for a BRCA1 founder mutation in families of West African ancestry. (1999) (62)
Characterization of EZH1, a human homolog of Drosophila Enhancer of zeste near BRCA1. (1996) (61)
Genetic epidemiology of breast and ovarian cancers. (1997) (61)
A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss. (2010) (60)
Precision medicine meets public health: population screening for BRCA1 and BRCA2. (2014) (60)
A Genomewide Screen for Suppressors of Alu-Mediated Rearrangements Reveals a Role for PIF1 (2012) (60)
Genetic influences on changes in body mass index: a longitudinal analysis of women twins. (1997) (59)
Evidence of genetic influence on central body fat in middle-aged twins. (1989) (58)
The search for BRCA1. (1994) (58)
Complex segregation analysis of primary hepatocellular carcinoma in Chinese families: interaction of inherited susceptibility and hepatitis B viral infection. (1991) (57)
Linkage of familial breast cancer to chromosome 17q21 may not be restricted to early-onset disease. (1992) (57)
Genetic Predisposition to Breast Cancer Due to Mutations Other Than BRCA1 and BRCA2 Founder Alleles Among Ashkenazi Jewish Women (2017) (57)
Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population (2006) (57)
Influence of host genotype on progression to acquired immunodeficiency syndrome among children infected with human immunodeficiency virus type 1. (1995) (57)
Genomic Views of Human History (1999) (56)
African-American HLA class II allele and haplotype diversity. (1996) (56)
Breast cancer genes: how many, where and who are they? (1992) (55)
Genomic views of human history. (1999) (54)
Complex germline rearrangement of BRCA1 associated with breast and ovarian cancer (2000) (54)
Normal renal parenchyma simulating tumor. (1968) (53)
Targeted long-read sequencing identifies missing disease-causing variation. (2021) (52)
Oncogenes and human breast cancer. (1989) (49)
Heritability of longitudinal changes in coronary-heart-disease risk factors in women twins. (1997) (47)
Imprisoning America: The social effects of mass incarceration (2005) (46)
Single nucleotide polymorphisms (SNPs) in the estrogen receptor gene and breast cancer susceptibility (1999) (46)
Formation of chimeric genes by copy-number variation as a mutational mechanism in schizophrenia. (2013) (45)
A novel approach to establishing permanent lymphoblastoid cell lines: Epstein-Barr virus transformation of cryopreserved lymphocytes. (1991) (45)
Loss of function germline mutations in RAD51D in women with ovarian carcinoma. (2012) (44)
Cisplatin with or without rucaparib after preoperative chemotherapy in patients with triple negative breast cancer: Final efficacy results of Hoosier Oncology Group BRE09-146. (2015) (44)
Environmental and behavioral determinants of fasting plasma glucose in women. A matched co-twin analysis. (1987) (43)
Influence of host genotype on progression to AIDS among HIV-infected men. (1991) (42)
The APC I1307K allele and breast cancer risk (1998) (41)
A Primate Genome Project Deserves High Priority (2000) (41)
A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA (2011) (41)
Further characterization of the DFNA1 audiovestibular phenotype. (1998) (41)
Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84 (2010) (40)
Nongenetic influences of obesity on other cardiovascular disease risk factors: an analysis of identical twins. (1990) (40)
Inherited breast cancer: an emerging picture (1998) (40)
A girl with West syndrome and autistic features harboring a de novo TBL1XR1 mutation (2014) (40)
Governing Work and Welfare in a New Economy: European and American Experiments (2005) (39)
Black Women’s Breakthrough into Clerical Work: An Occupational Tipping Model (1993) (37)
Human genetics and human rights: Identifying the families of kidnapped children (1984) (37)
Hardy-Weinberg testing for HLA class II (DRB1, DQA1, DQB1, and DPB1) loci in 26 human ethnic groups. (1999) (37)
BARD1 is necessary for ubiquitylation of nucleosomal histone H2A and for transcriptional regulation of estrogen metabolism genes (2018) (36)
Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in thrombopoietin. (2017) (36)
Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15 (2009) (36)
International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation (2011) (34)
Intensive Surveillance with Biannual Dynamic Contrast-Enhanced Magnetic Resonance Imaging Downstages Breast Cancer in BRCA1 Mutation Carriers (2018) (33)
Evidence of a founder BRCA1 mutation in Scotland (2000) (33)
CCR5del32 in perinatal HIV-1 infection. (1997) (33)
Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and Surveillance. (2017) (33)
50 – DETERMINATION OF FAMILIAL RELATIONSHIPS (1989) (32)
Synergy between T cell receptor beta gene polymorphism and HLA-DR4 in susceptibility to rheumatoid arthritis. (1996) (32)
Identifying Inherited and Acquired Genetic Factors Involved in Poor Stem Cell Mobilization and Donor-Derived Malignancy. (2015) (32)
Inherited thrombocytopenia associated with mutation of UDP‐galactose‐4‐epimerase (GALE) (2018) (31)
Genetic risk factors for perinatally acquired HIV-1 infection. (1992) (30)
Risk factors for benign breast disease: a case-control study of discordant twins. (1984) (30)
Leiomyosarcoma of the duodenum. Angiographic findings and report of a case. (1968) (29)
Germline variants drive myelodysplastic syndrome in young adults (2021) (29)
Genomic analysis of inherited breast cancer among Palestinian women: Genetic heterogeneity and a founder mutation in TP53 (2017) (29)
FAM111B Mutation Is Associated With Inherited Exocrine Pancreatic Dysfunction (2016) (28)
Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadism. (2015) (28)
Genetic susceptibility to AIDS: absence of an association with group-specific component (Gc) (1987) (28)
BRCA1 and BRCA2 mutations in Ashkenazi Jewish families with breast and ovarian cancer. (1997) (28)
SeqHelp: a program to analyze molecular sequences utilizing common computational resources. (1998) (28)
MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15‐CD2 Isoform (2016) (28)
Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1 (2018) (28)
Collaborative genomics for human health and cooperation in the Mediterranean region (2010) (27)
Vesicular acetylcholine transporter defect underlies devastating congenital myasthenia syndrome (2017) (27)
A truncating mutation in GPSM2 is associated with recessive non‐syndromic hearing loss (2012) (27)
A novel sodium bicarbonate cotransporter-like gene in an ancient duplicated region: SLC4A9 at 5q31 (2001) (27)
Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infection (2016) (27)
Genomic structure and evolutionary context of the human feline leukemia virus subgroup C receptor (hFLVCR) gene: evidence for block duplications and de novo gene formation within duplicons of the hFLVCR locus. (2002) (26)
Systematic misclassification of missense variants in BRCA1 and BRCA2 “coldspots” (2020) (26)
Using Somatic Mutations from Tumors to Classify Variants in Mismatch Repair Genes. (2018) (26)
Cisplatin with or without rucaparib after preoperative chemotherapy in patients with triple-negative breast cancer (TNBC): Hoosier Oncology Group BRE09-146. (2014) (24)
Heterogeneity analysis of breast cancer families by using age at onset as a covariate. (1992) (24)
Characterization of splice-altering mutations in inherited predisposition to cancer (2019) (24)
Whole Exome Sequencing Identifies Candidate Genes Associated with Hereditary Predisposition to Uveal Melanoma. (2019) (24)
A novel disease-causing synonymous exonic mutation in GATA2 affecting RNA splicing. (2018) (22)
Squaring up : policy strategies to raise women's incomes in the United States (2001) (22)
Are African-Americans Losing Their Footholds in Better Jobs? (1998) (22)
Hodgkin's disease susceptibility: linkage to the HLA locus demonstrated by a new concordance method. (1983) (22)
Gene Discovery for Complex Traits: Lessons from Africa (2017) (22)
Mitochondrial PITRM1 peptidase loss-of-function in childhood cerebellar atrophy (2018) (22)
The APCI1307K allele and breast cancer risk. (1998) (22)
An application of DNA sequencing to a human rights problem. (1991) (22)
Sexual orientation and the X (1993) (21)
Rare HRAS alleles and susceptibility to human breast cancer. (1990) (21)
BRCA2 in Ovarian Development and Function. Reply. (2019) (21)
New data on glucose-6-phosphate dehydrogenase deficiency in Saudi Arabia. G6PD variants, and the association between enzyme deficiency and hemoglobins S. (1977) (21)
Long terminal repeat and nef gene variants of human immunodeficiency virus type 1 in perinatally infected long-term survivors and rapid progressors. (1997) (21)
Diagnosis of twin zygosity by self-assessment and by genetic analysis. (1980) (21)
Genomic analysis of inherited hearing loss in the Palestinian population (2020) (20)
Occupational Segregation by Race and Sex in Brazil, 1989-2001 (2009) (20)
De novo mutation in RING1 with epigenetic effects on neurodevelopment (2018) (20)
Genetics of hearing loss in the Arab population of Northern Israel (2018) (19)
The significance of the renal capsular arteries. (1967) (19)
Reply to “…and secreted tumour suppressors” (1996) (18)
The inheritance of immunoglobulin E: genetic linkage analysis. (1983) (17)
Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria (2011) (17)
The Door in the Dream: Conversations With Eminent Women in Science (2000) (17)
Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families (2016) (17)
CRISPR–Cas9/long-read sequencing approach to identify cryptic mutations in BRCA1 and other tumour suppressor genes (2020) (17)
Human Capital and Black Women's Occupational Mobility (1995) (16)
Genetic analysis of cancer in families. (1990) (16)
Genetic analysis of human breast cancer: A synthesis of contributions to Gaw IV (1986) (16)
Betwixt and Between: The Spectrum of Formality Revealed in the Labor Market Experiences of Mexican Migrant Workers in the United States (2009) (16)
Localization of the early-onset breast cancer gene. (1991) (15)
Human genetics. Mapping human history. (2002) (15)
Identification of a new BRCA2 large genomic deletion associated with high risk male breast cancer (2015) (15)
A novel BRCA2-binding protein and breast and ovarian tumorigenesis. (2004) (15)
Black women’s labor market status: Occupational segregation in the United States and Great Britain (1995) (15)
Genetic analysis of cystic fibrosis: linkage of DNA and classical markers in multiplex families. (1986) (15)
Inheritance of the shared epitope and long‐term outcomes of rheumatoid arthritis among community‐based Caucasian females (1998) (15)
Clinical usefulness of genetic information for predicting radiographic damage in rheumatoid arthritis. (2002) (15)
Deep sequencing with intronic capture enables identification of an APC exon 10 inversion in a patient with polyposis (2014) (14)
Even Gary Becker Wouldn't Call Them Altruists! The Case of Mexican Migration: A Reply to Sana And Massey, "SSQ" June 2005 (2007) (14)
What Sustainability Should Mean (2008) (14)
Genomic sequencing in the service of human rights. (2002) (14)
Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic Analysis (2016) (14)
Telomere biology disorder prevalence and phenotypes in adults with familial hematologic and/or pulmonary presentations. (2020) (14)
Response: Why It Is Time to Sequence (2010) (14)
Two independent polymorphisms at the 17 beta-hydroxysteroid dehydrogenase (EDH17B) gene (17q21). (1993) (13)
Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive disease (2016) (13)
Germline Mutations of Inhibins in Early-Onset Ovarian Epithelial Tumors (2013) (13)
Genetic markers and cancer epidemiology (1977) (13)
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1 (2020) (12)
MHC class II alleles associated with clinical and immunological manifestations of HIV-1 infection among children in Catalonia, Spain. (1996) (12)
A functional assay for mutations in tumor suppressor genes caused by mismatch repair deficiency. (2001) (12)
Alpha‐thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation – c.109C>T (p.R37X) (2015) (12)
Unusual radiologic features of pheochromocytoma. (1969) (12)
Exclusion of the retinoblastoma gene and chromosome 13q as the site of a primary lesion for human breast cancer. (1990) (11)
Mutations in homologous recombination genes and response to treatment in GOG 218: An NRG Oncology study (2016) (11)
Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy and enteropathy, and implications for clinical management. (2021) (11)
Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fcγ receptor gene region (1991) (10)
Relative predispositional effects and mode of inheritance of HLA‐DRB1 alleles among community‐based Caucasian females with rheumatoid arthritis (1998) (10)
Effects of germline and somatic events in candidate BRCA-like genes on breast-tumor signatures (2020) (10)
The Great Adventure of an American Human Geneticist. (2016) (10)
Population Genetics of BRCA 1 and BRCA 2 (2006) (10)
Association of duffy blood groups with the suckle cell trait (1976) (10)
“Race riots” and black economic progress (2003) (10)
Haplotype analyses of the c.1027C>T and c.2167_2168delAT recurrent truncating mutations in the breast cancer-predisposing gene PALB2 (2016) (9)
Abundant novel transcriptional units and unconventional gene pairs on human chromosome 22. (2005) (9)
Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fcγ receptor gene region (2004) (9)
Inherited predisposition to malignant mesothelioma (MM) due to mutations in DNA repair genes. (2018) (9)
My Mother Will Never Forgive Them (1992) (9)
Beyond market‐fundamentalist economics: an agenda for heterodox economics to change the dominant narrative (2012) (9)
Dermatological manifestations of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis (POIKTMP): a case series of 28 patients (2019) (8)
Interdisciplinarity and Systems Thinking: some implications for engineering education and education for industry (1988) (8)
Cisplatin +/− rucaparib after preoperative chemotherapy in patients with triple-negative or BRCA mutated breast cancer (2021) (8)
Characteristics of smoking- discordant monozygotic twins. (1981) (8)
Leaving Kansas … finding genes in 1997 (1997) (8)
The Drama of J.M. Synge (1985) (8)
Genetic analysis of human breast cancer: Literature review and description of family data in workshop (1986) (8)
Keeping people in their place: An exploratory analysis of the role of violence in the maintenance of “property rights” in race and gender privileges in the United States (1999) (7)
Cholecystokinin cholecystography in the diagnosis of acalculous extrahepatic biliary tract disorders. (1978) (7)
Genetic analysis of breast and ovarian cancer in families. (1994) (7)
Inherited mutations in breast cancer genes in African American breast cancer patients revealed by targeted genomic capture and next-generation sequencing. (2013) (7)
Identification of BRCA1/BRCA2 carriers by screening in the healthy population and its implications. (2011) (7)
Variable Features of Juvenile Polyposis Syndrome With Gastric Involvement Among Patients With a Large Genomic Deletion of BMPR1A (2019) (7)
African-American HLA class II allele and haplotype diversity. (1996) (7)
Genetic epidemiology of low density lipoprotein subclasses a common allele predisposing to coronary heart disease (1986) (6)
Duffy blood group and malaria. (1976) (6)
Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene region. (1991) (6)
ONE OF THE AUTHORS REPLIES (1987) (6)
Screening for abnormal hemoglobins in the middle east: new data on hemoglobin S and the presence of hemoglobin C in Saudi Arabia. (1976) (6)
Differences in Wage Levels Among Metropolitan Areas: Less-educated Workers in the United States (2000) (6)
Latinas and African American Women at Work: Race, Gender, and Economic Inequality, edited by Irene Browne (2000) (6)
Mexican Women and Work on Both Sides of the U.S.‐Mexican Border (2011) (6)
2012 Presidential Address: The scientist as a citizen of the world. (2013) (6)
Genomic structure of chromosome 17 deletions in BRCA1-associated ovarian cancers. (2008) (6)
Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsy (2021) (6)
Inherited predisposition to breast cancer in the Carolina Breast Cancer Study (2021) (6)
Polymorphisms of mitochondrially encoded proteins. (1986) (6)
A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizures (2020) (6)
Not just Salk (2017) (5)
Genetic variation among the Mapuche Indians from the Patagonian region of Argentina (1993) (5)
Hiding in Plain Sight - Somatic Mutation in Human Disease. (2020) (5)
Contribution of InheritedMutations in the BRCA 2-Interacting Protein PALB 2 to Familial Breast Cancer (2011) (5)
Working out Social Sustainability on the Ground (2008) (5)
Strong Families or Patriarchal Economies? Southern European Labor Markets and Welfare in Comparative Perspective (2002) (5)
NKX2-2 mutation causes congenital diabetes and infantile obesity with paradoxical glucose induced ghrelin secretion. (2020) (5)
Geriatric gynecology. (2012) (5)
Laterality of breast cancer in families. (1979) (4)
Novel transcriptional units and unconventional gene pairs in the human genome: toward a sequence-level basis for primate-specific phenotypes? (2003) (4)
Eye color and hypertension. (1990) (4)
The Sustainability Debate: Dj Vu All Over Again (2009) (4)
Arteriovenous fistula of external carotid artery. (1968) (4)
Proposed shift in screening for breast cancer--reply. (2015) (4)
Three Cheers for Irish Drama@@@The Drama of J. M. Synge@@@A Critical History of Modern Irish Drama, 1891-1980@@@A Guide to O'Casey's Plays: From the Plough to the Stars (1987) (4)
Adaptation and validation of a computerized neurocognitive battery in the Xhosa of South Africa. (2021) (4)
Helping battered women: A study of the relationship between nurses' education and experience and their preferred models of helping (1988) (4)
Genetics and molecular biology of breast cancer (1992) (3)
Detection of Mutations in Inherited Bone Marrow Failure and Myelodysplastic Syndrome Genes Using Genomic Capture and Massively Parallel Sequencing in Clinical Diagnostics (2016) (3)
Male Influences on Cervical Cancer Risk (1987) (3)
Corrigendum to: Loss of function germline mutations in RAD51D in women with ovarian carcinoma [Gynecol Oncol 127: 552–555, 2012] (2014) (3)
"Ni Uno Ni El Otro": The Spectrum of Formality In The U.S. Work Experience of Mexican Migrants In Portland, Oregon (2010) (3)
Germline mutations in cancer susceptibility genes in brca1 and brca2 negative families with ovarian and breast cancer (2014) (3)
Breast cancer risks for BRCA 1/2 carriers [2] (multiple letters) (2004) (3)
Assessment of the Socio-Economic Impacts of SB 1080 on Immigrant Groups (2011) (3)
Inherited mutations in breast cancer genes in African American breast cancer patients revealed by targeted genomic capture and next generation sequencing. (2013) (2)
BROCA gene panel testing in African descendants from northeastern Brazil: Genetic susceptibility profile of an admixed population. (2017) (2)
Abstract P3-07-05: Frequent BRCA1 and BRCA2 mutations are found in Mexican and Mexican-American women with breast cancer (2013) (2)
Solution structure of the BRCA1/BARD1 RING-domain heterodimer (2001) (2)
Hermeneutics of Suspicion: Nativism, Nationalism. and the Language Question in "Oxen of the Sun" (1998) (2)
Mutational spectrum of breast cancer susceptibility genes among women ascertained in a cancer risk clinic in Northeast Brazil (2022) (2)
Green pigs, red herrings, and a golden hoe: a retrospective on the identification of BRCA1 and the beginning of its characterization. (1994) (2)
Allan C. Wilson (1934–91): In memoriam Mary-Claire King. (1992) (2)
Arno G. Motulsky (1923–2018): A Founder of Medical Genetics, Creator of Pharmacogenetics, and Former ASHG President (2018) (2)
Costume evolution during the development of romantic relationships and its impact on the positions of power in the Star Wars prequel and original trilogies (2019) (2)
The gene for pancreatic polypeptide (PPY) and the anonymous marker D17S78 are within 45 kb of each other on chromosome 17q21. (1994) (2)
LEWIS NEGATIVE GENOTYPE AND BREAST CANCER RISK (1989) (2)
Genetic epidemiology of persistent islet cell antibodies among IDDM patients (1989) (2)
A tipping point in neuropsychiatric genetics (2021) (2)
J. M. Synge, ‘national’ drama and the post-Protestant imagination (2004) (2)
Evidence is evidence: an interview with Mary-Claire King. Interviewed by Jane Gitschier. (2013) (2)
Strong Families or Patriarchal Economies? 'Familial' Labor Markets and Welfare States in Comparative Perspective (2002) (2)
Should black women and men live in the same place? An intermetropolitan assessment of relative labor market success (1999) (2)
The Applications of Molecular Evolution to Systematics: Rates, Regulation, and the Role of Natural Selection (1977) (2)
Testing Ashkenazi Jewish Women for Mutations Predisposing to Breast Cancer in Genes Other Than BRCA1 and BRCA2-Reply. (2018) (1)
Deep sequencing reveals a high rate of temporal heterogeneity of somatic mutations in paired primary and recurrent ovarian carcinomas (2013) (1)
Human genetics. Sexual orientation and the X. (1993) (1)
Novel Functional Screen for New Breast Cancer Genes (2004) (1)
An Interview with Marianne Ferber: Founding feminist economist (1999) (1)
The female fan goes shopping: Satisfaction, involvement and utilitarian value when shopping for women’s Star Wars merchandise (2019) (1)
OR13-002 Recessive mutations in CECR1, encoding adenosine deaminase 2 (ADA2), cause systemic and cutaneous polyarteritis nodosa (PAN) (2013) (1)
Nongenetic Influences ofObesity on OtherCardiovascular Disease Risk Factors: AnAnalysis ofIdentical Twins (1990) (1)
Helicase-inactivating BRIP1 mutation yields Fanconi anemia with microcephaly and other congenital abnormalities (2020) (1)
10 — Focused PlenaryGermline mutations in DNA repair genes in women with ovarian, peritoneal, or fallopian tube cancer treated on GOG protocols 218 and 262 (2014) (1)
Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15 (2009) (1)
Identification of a new BRCA2 large genomic deletion associated with high risk male breast cancer (2015) (1)
Germline mutations in DNA repair genes in women with ovarian, peritoneal, or fallopian tube cancer treated on GOG protocols 218 and 262 (2013) (1)
Complete Genomic Sequence and Analysis of 117 kb of Human DNA Containing the Gene BRCAI (2007) (1)
Women’s Work: Using U.S. History to Explain Mexican Women’s Differential Work Strategies in Mexico and the United States (2006) (1)
Abstract AS09: Germline mutations in cancer susceptibility genes in BRCA1 and BRCA2 negative families with ovarian and breast cancer (2015) (1)
Forum: The interplay of genes and environment in psychiatric disorders. (2008) (1)
Defining women at high risk of ovarian cancer. (2007) (1)
Risk factors in breast cancer. (1981) (1)
A novel founder MSH2 deletion in Ethiopian Jews is mainly associated with early-onset colorectal cancer (2021) (1)
Of Mice and Women: Genetic Analysis of Breast Cancer In Families (1986) (1)
Gene mapping of a simulated complex disease. (1989) (1)
Report on Genetic Epidemiology workshop I, held at Shanghai Medical University, December 24–31, 1988 (1990) (1)
InheritedMutations inWomenWith Ovarian Carcinoma (2016) (1)
Gender, Color, Caste, and Class (2002) (1)
Inheritance and Possible Coinheritance of HLA-Linked Susceptibilities to Insulin-Dependent Diabetes Mellitus, Autoimmune Thyroid Diseases, and Rheumatoid Arthritis (1984) (1)
Contribution of InheritedMutations in the BRCA2-Interacting Protein PALB2 to Familial Breast Cancer (2011) (1)
"Inherited Breast and Ovarian Cancer: From Gene Discovery to Population Screening" (2015) (0)
ACS focusing on breast cancer detection. (1992) (0)
Effects of cholecystokinin octapeptide (CCK OP) on hypothalamic electrical activity (1975) (0)
Next generation sequencing to identify inherited mutations in all breast cancer genes in three breast cancer cohorts (2013) (0)
343. From Gene Discovery to Diagnosis and Treatment: Breast Cancer as a Perhaps Unlikely Model for Mental Illness (2017) (0)
Clinically Complex LRBA Deficiency Due to a Founder Allele in the Georgian Jewish Population (2022) (0)
Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss. (2023) (0)
Inherited predisposition to breast cancer in the Carolina Breast Cancer Study (2021) (0)
Massive parallel sequencing identifies novel ovarian cancer susceptibility genes and a high fraction of hereditary ovarian, peritoneal and tubal carcinomas (2011) (0)
Environmental and Lifestyle Influences on Breast Cancer Risk: Clues from Women with Inherited Mutations in BRCA1 and BRCA2 (1999) (0)
Genetics of hearing loss in the Arab population of Northern Israel (2018) (0)
Services DRAFT meeting summary Summary of the Symposium on Genetic Variation and Gene Environment Interaction in Human Health and Disease April 16 , 2003 (2003) (0)
2020 William Allan Award address: genetics as a way of thinking-cultural inheritance from our teachers. (2021) (0)
P478. Functional Characterization of Rare and Protein-Damaging Mutations in Patients With Sporadic Schizophrenia Using CRISPRi in iPSCs (2022) (0)
TWINNING IN AUSTRALIA : AN UNCONTROLLED SURVEY OF 1000 MULTIPLE BIRTHS (2016) (0)
ASHG AWARDS AND ADDRESSES 2012 Presidential Address: The Scientist as a Citizen of the World 1 (2013) (0)
INVITED EDITORIAL Inherited Predisposition to Breast and Ovarian Cancer (2007) (0)
Association of Genetic Diagnoses of Childhood-Onset Hearing Loss With Cochlear Implant Outcomes. (2023) (0)
Markers of BRCAness in breast cancer (2019) (0)
MULTIPLE RARE ALLELES IN A GENETICALLY HETEROGENEOUS DISEASE (2010) (0)
Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum Disorder (2021) (0)
Effects of germline and somatic events in candidate BRCAness genes on breast-tumor signatures (2019) (0)
Factors associated with genetic testing in BRCA1 and BRCA2 mutation carriers with advanced ovarian carcinoma (2011) (0)
Genetics and Genomics: A Call for Papers (2007) (0)
Mutations in Families at High Risk for Breast Cancer—Reply (2006) (0)
Genetic marker for breast and ovarian cancer (1996) (0)
Genetic Alterations in Familial Breast Cancer: Mapping and Cloning Genes Other Than BRCAl (1995) (0)
Transcriptional Regulation of BRCA1 (1998) (0)
Gene mutations and cognitive delay - Response (2008) (0)
In Reply [9] (2006) (0)
Abstract A12: Mutations in homologous recombination genes and response to treatment in GOG 218: An NRG Oncology Study. (2016) (0)
Mutations in ATM, Radiation Exposure and Breast Cancer Risk Among Black and White Women (1997) (0)
Genomic analysis of human breast cancer in families and populations (2005) (0)
GENETIC MARKERS FOR BREAST AND OVARIAN CANCER (1997) (0)
Breast-Cancer Risk in Families With Mutations in PALB2 EDITORIAL COMMENT (2014) (0)
2016 ASHG Awards and Addresses. (2017) (0)
Germline and somatic mutations in homologous recombination genes predict platinum response in ovarian, fallopian tube, and peritoneal carcinomas (2012) (0)
Thanks to reviewers (2006) (0)
An Interview with Barbara Bergmann: Leading feminist economist (2000) (0)
Erratum: Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fcγ receptor gene region (Human Genetics (1991) 88 (1-12)) (1993) (0)
Phase I Trial of Retroviral BRCA 1 sv Gene Therapy in Ovarian Cancer 1 (2005) (0)
Book Review: Ex Mex: From Migrants to Immigrants By Jorge G. Castañeda. New York: The New Press, 2007. 222 pp. $25.95 hardback (2009) (0)
Cisplatin +/− rucaparib after preoperative chemotherapy in patients with triple-negative or BRCA mutated breast cancer (2021) (0)
Microeeonomics in Context (2006) (0)
Book Review: Growing Public: Social Spending and Economic Growth since the Eighteenth Century (2006) (0)
Whole Genome Sequencing of High-Risk Families to Identify New Mutational Mechanisms of Breast Cancer Predisposition (2014) (0)
Lasker Award Winner Mary-Claire King (2014) (0)
906 De novomutations in childhood-onset systemic lupus erythematosus (2022) (0)
Systematic misclassification of missense variants in BRCA1 and BRCA2 “coldspots” (2020) (0)
Book Review: Organizing Immigrants: The Challenge for Unions in Contemporary California (2004) (0)
"Apes and Humans are 99% similar." Background (2012) (0)
Reply to Tzoulis et al.: Genetic and clinical heterogeneity of essential tremor (2015) (0)
Keeping People in Their Place: An Exploratory Analysis of the Role of Violence in the Maintenance of "Property Rights" in Race and Gender Privileges in the United States (1999) (0)
Germline and somatic mutations in homologous recombination genes predict platinum response and improved overall survival in ovarian, fallopian tube, and peritoneal carcinomas (2013) (0)
The Theatre of Nation: Irish Drama and Cultural Nationalism 1890-1916 by Ben Levitas, and: Theatre and the State in Twentieth-Century Ireland: Cultivating the People by Lionel Pilkington, and: A History of the Irish Theatre 1601-2000 by Christopher Morash (review) (2022) (0)
Anthropology and Reductionism Reflections about DNA studies , reductionism and the role of Anthropology (2006) (0)
Genetics and genomics: a call for papers. (2007) (0)
The Scientist as World Citizen (2012) (0)
Homologous recombination defects are common in non-serous ovarian, fallopian tube, and peritoneal carcinomas (2013) (0)
Conjuring past or Future? Versions of Synge's 'Play of '98' (2000) (0)
Introducing Race and Gender into Economics, edited by Robin L. Bartlett (2000) (0)
Jobs and Gender: Does Sex Play a Role in the Region's Recession? (2010) (0)
439. Functional Characterization of Damaging Mutations in Patients With Sporadic Schizophrenia Using CRISPRi in iPSCS (2023) (0)
Invited Editorial: Genetic Testing of Identity and Relationship' (2006) (0)
An Assessment of Three (Somewhat) Competitive Explanations for Black Women's Recent Breakthrough into Clerical Work (1994) (0)
A Healthy Son (2011) (0)
Index rerum ad Vol. 56, 1976 (1976) (0)
Comprehensive Genomic Evaluation For Inherited Bone Marrow Failure/Myelodysplastic Syndromes (2013) (0)
Genomic and Functional Analysis of De Novo Nonsense Mutation in a Chromatin Remodeling Gene in a Patient With Sporadic Schizophrenia (2020) (0)
NKX2-2 mutation causes congenital diabetes and infantile obesity with paradoxical glucose-induced ghrelin secretion. (2021) (0)
Index autorum ad Vol. 56, 1976 (1976) (0)
Contents, Vol. 56, 1676 (1976) (0)

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