Works matching AU King, Claire

Results: 116

Inherited mutations in cancer susceptibility genes are common among survivors of breast cancer who develop therapy-related leukemia.

Published in:

2016

By:

Churpek, Jane E.;
Marquez, Rafael;
Neistadt, Barbara;
Claussen, Kimberly;
Lee, Ming K.;
Churpek, Matthew M.;
Huo, Dezheng;
Weiner, Howard;
Bannerjee, Mekhala;
Godley, Lucy A.;
Le Beau, Michelle M.;
Pritchard, Colin C.;
Walsh, Tom;
King, Mary‐Claire;
Olopade, Olufunmilayo I.;
Larson, Richard A.;
King, Mary-Claire

Publication type:

journal article

Not Your Mom's Dollhouse: Miniatures, Mediation, and Trauma.

Published in:

Women's Studies in Communication, 2025, v. 48, n. 2, p. 249, doi. 10.1080/07491409.2025.2483693

By:

King, Claire Sisco

Publication type:

Article

A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizures.

Published in:

Neurogenetics, 2020, v. 21, n. 4, p. 259, doi. 10.1007/s10048-020-00615-4

By:

Segel, Reeval;
Aran, Adi;
Gulsuner, Suleyman;
Nakamura, Hiroki;
Rosen, Tzvia;
Walsh, Tom;
Denda, Hiroto;
Zeligson, Sharon;
Eto, Katsuki;
Beeri, Rachel;
Okai, Haruka;
King, Mary-Claire;
Levy-Lahad, Ephrat;
Funato, Kouichi;
Renbaum, Paul

Publication type:

Article

Relative predispositional effects and mode of inheritance of HLA-DRB1 alleles among community-based Caucasian females with rheumatoid arthritis.

Published in:

Genetic Epidemiology, 1998, v. 15, n. 2, p. 123, doi. 10.1002/(SICI)1098-2272(1998)15:2<123::AID-GEPI2>3.0.CO;2-7

By:

Mu, Hua;
King, Mary-Claire;
Criswell, Lindsey A.

Publication type:

Article

Inheritance of the shared epitope and long-term outcomes of rheumatoid arthritis among community-based Caucasian females.

Published in:

Genetic Epidemiology, 1998, v. 15, n. 1, p. 61, doi. 10.1002/(SICI)1098-2272(1998)15:1<61::AID-GEPI5>3.0.CO;2-7

By:

Criswell, Lindsey A.;
Mu, Hua;
Such, Carol L.;
King, Mary-Claire

Publication type:

Article

MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform.

Published in:

Human Mutation, 2016, v. 37, n. 5, p. 481, doi. 10.1002/humu.22961

By:

Grati, M'hamed;
Yan, Denise;
Raval, Manmeet H.;
Walsh, Tom;
Ma, Qi;
Chakchouk, Imen;
Kannan‐Sundhari, Abhiraami;
Mittal, Rahul;
Masmoudi, Saber;
Blanton, Susan H.;
Tekin, Mustafa;
King, Mary‐Claire;
Yengo, Christopher M.;
Liu, Xue Zhong

Publication type:

Article

Germline Mutations of Inhibins in Early-Onset Ovarian Epithelial Tumors.

Published in:

Human Mutation, 2014, v. 35, n. 3, p. 294, doi. 10.1002/humu.22489

By:

Tournier, Isabelle;
Marlin, Régine;
Walton, Kelly;
Charbonnier, Françoise;
Coutant, Sophie;
Théry, Jean‐Christophe;
Charbonnier, Camille;
Spurrell, Cailyn;
Vezain, Myriam;
Ippolito, Lorena;
Bougeard, Gaëlle;
Roman, Horace;
Tinat, Julie;
Sabourin, Jean‐Christophe;
Stoppa‐Lyonnet, Dominique;
Caron, Olivier;
Bressac‐de Paillerets, Brigitte;
Vaur, Dominique;
King, Mary‐Claire;
Harrison, Craig

Publication type:

Article

A Single Man and a Tragic Woman.

Published in:

2014

By:

King, Claire Sisco

Publication type:

Film/TV Criticism and Review

Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families.

Published in:

European Journal of Human Genetics, 2010, v. 18, n. 4, p. 407, doi. 10.1038/ejhg.2009.190

By:

Shahin, Hashem;
Walsh, Tom;
Rayyan, Amal Abu;
Lee, Ming K.;
Higgins, Jake;
Dickel, Diane;
Lewis, Kristen;
Thompson, James;
Baker, Carl;
Nord, Alex S.;
Stray, Sunday;
Gurwitz, David;
Avraham, Karen B.;
King, Mary-Claire;
Kanaan, Moien

Publication type:

Article

Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15.

Published in:

2009

By:

Doucette, Lance;
Merner, Nancy D;
Cooke, Sandra;
Ives, Elizabeth;
Galutira, Dante;
Walsh, Vanessa;
Walsh, Tom;
MacLaren, Linda;
Cater, Tracey;
Fernandez, Bridget;
Green, Jane S;
Wilcox, Edward R;
Shotland, Larry;
Li, X C;
Lee, Ming;
King, Mary-Claire;
Young, Terry-Lynn

Publication type:

Correction Notice

Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15.

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 5, p. 554, doi. 10.1038/ejhg.2008.231

By:

Doucette, Lance;
Merner, Nancy D.;
Cooke, Sandra;
Ives, Elizabeth;
Galutira, Dante;
Walsh, Vanessa;
Walsh, Tom;
MacLaren, Linda;
Cater, Tracey;
Fernandez, Bridget;
Green, Jane S.;
Wilcox, Edward R.;
Shotland, Larry;
Li, X. C.;
Lee, Ming;
King, Mary-Claire;
Young, Terry-Lynn

Publication type:

Article

Family carers providing support to a person dying in the home setting: A narrative literature review.

Published in:

Palliative Medicine, 2015, v. 29, n. 6, p. 487, doi. 10.1177/0269216314565706

By:

Morris, Sara M;
King, Claire;
Turner, Mary;
Payne, Sheila

Publication type:

Article

Genetic markers and cancer epidemiology.

Published in:

Cancer (0008543X), 1977, v. 39, n. S4, p. 1861, doi. 10.1002/1097-0142(197704)39:4+<1861::AID-CNCR2820390819>3.0.CO;2-I

By:

Petrakis, Nicholas L.;
King, Mary-Claire

Publication type:

Article

The Door in the Dream: Conversations With Eminent Women in Science.

Published in:

2000

By:

King, Mary-Claire

Publication type:

Book Review

Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy.

Published in:

Nature Genetics, 2015, v. 47, n. 2, p. 180, doi. 10.1038/ng.3177

By:

Gyurkocza, Boglarka;
Hofmann, Inga;
Marquez, Rafael;
King, Mary-Claire;
Loeb, Keith R;
Delrow, Jeffrey J;
Forouhar, Melissa;
Coats, Scott A;
Churpek, Jane E;
Neistadt, Barbara;
Godley, Lucy A;
Walsh, Tom;
Basom, Ryan S;
Horwitz, Marshall S;
Shimamura, Akiko;
Abkowitz, Janis L;
Gulsuner, Suleyman;
Pritchard, Colin C;
Zhang, Michael Y;
Sanchez-Bonilla, Marilyn

Publication type:

Article

Collaborative genomics for human health and cooperation in the Mediterranean region.

Published in:

Nature Genetics, 2010, v. 42, n. 8, p. 641, doi. 10.1038/ng0810-641

By:

Özçelik, Tayfun;
Kanaan, Moien;
Avraham, Karen B.;
Yannoukakos, Drakoulis;
Mégarbané, André;
Tadmouri, Ghazi O.;
Middleton, Lefkos;
Romeo, Giovanni;
King, Mary-Claire;
Levy-Lahad, Ephrat

Publication type:

Article

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13).

Published in:

Nature Genetics, 1999, v. 23, n. 4, p. 413, doi. 10.1038/70516

By:

McGuirt, Wyman T.;
Prasad, Sai D.;
Griffith, Andrew J.;
Kunst, Henricus P.M.;
Green, Glenn E.;
Shpargel, Karl B.;
Runge, Christina;
Huybrechts, Christy;
Mueller, Robert F.;
Lynch, Eric;
King, Mary-Claire;
Brunner, Han G.;
Cremers, Cor W.R.J.;
Takanosu, Masamine;
Li, Shi-Wu;
Arita, Machiko;
Mayne, Richard;
Prockop, Darwin J.;
Camp, Guy Van

Publication type:

Article

The APC I1307K allele and breast cancer risk.

Published in:

Nature Genetics, 1998, v. 20, n. 1, p. 13, doi. 10.1038/1666

By:

Redston, Mark;
Nathanson, Katherine L.;
Yuan, Zhi Qiang;
Neuhausen, Susan L.;
Satagopan, Jaya;
Wong, Nora;
Yang, Diana;
Nafa, Doudja;
Abrahamson, John;
Ozcelik, Hilmi;
Antin-Ozerkis, Danielle;
Andrulis, Irene;
Daly, Mary;
Pinsky, Leonard;
Schrag, Deborah;
Gallinger, Steven;
Kaback, Michael;
King, Mary-Claire;
Woodage, Trevor

Publication type:

Article

Accurate and exact CNV identification from targeted high-throughput sequence data.

Published in:

BMC Genomics, 2011, v. 12, p. 1, doi. 10.1186/1471-2164-12-184

By:

Nord, Alex S;
Lee, Ming;
King, Mary-Claire;
Walsh, Tom

Publication type:

Article

Accurate and exact CNV identification from targeted high-throughput sequence data.

Published in:

BMC Genomics, 2011, v. 12, n. 1, p. 184, doi. 10.1186/1471-2164-12-184

By:

Nord, Alex S.;
Ming Lee;
King, Mary-Claire;
Walsh, Tom

Publication type:

Article

Comparative analysis of cancer genes in the human and chimpanzee genomes.

Published in:

BMC Genomics, 2006, v. 7, p. 15, doi. 10.1186/1471-2164-7-15

By:

Puente, Xose S;
Velasco, Gloria;
Gutierrez-Fernandez, Ana;
Bertranpetit, Jaume;
King, Mary-Claire;
Lopez-Otin, Carlos

Publication type:

Article

Complex germline rearrangement of BRCA1 associated with breast and ovarian cancer.

Published in:

Genes, Chromosomes & Cancer, 2000, v. 29, n. 1, p. 58, doi. 10.1002/1098-2264(2000)9999:9999<::AID-GCC1008>3.0.CO;2-F

By:

Payne, Shannon R.;
Newman, Beth;
King, Mary-Claire

Publication type:

Article

Introduction.

Published in:

QED: A Journal in GLBTQ Worldmaking, 2018, v. 5, n. 2, p. 53, doi. 10.14321/qed.5.2.0053

By:

King, Claire Sisco

Publication type:

Article

Genetic risk factors for perinatally acquired HIV-1 infection.

Published in:

1992

By:

Just, Jeanette;
Louie, Leslie;
Abrams, Elaine;
Nicholas, Stephen W.;
Wara, Diane;
Stein, Zena;
King, Mary-Claire;
Just, J;
Louie, L;
Abrams, E;
Nicholas, S W;
Wara, D;
Stein, Z;
King, M C

Publication type:

journal article

Car Crashes and Crosses to Bear: Trauma and Masculinity in Seven Pounds.

Published in:

2012

By:

KING, CLAIRE SISCO

Publication type:

Film/TV Criticism and Review

A Genomewide Screen for Suppressors of Alu-Mediated Rearrangements Reveals a Role for PIF1.

Published in:

PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0030748

By:

Chisholm, Karen M.;
Aubert, Sarah D.;
Freese, Krister P.;
Zakian, Virginia A.;
King, Mary-Claire;
Welcsh, Piri L.

Publication type:

Article

BRCA1, TP53, and CHEK2 germline mutations in uterine serous carcinoma.

Published in:

Cancer (0008543X), 2013, v. 119, n. 2, p. 332, doi. 10.1002/cncr.27720

By:

Pennington, Kathryn P.;
Walsh, Tom;
Lee, Ming;
Pennil, Christopher;
Novetsky, Akiva P.;
Agnew, Kathy J.;
Thornton, Anne;
Garcia, Rochelle;
Mutch, David;
King, Mary‐Claire;
Goodfellow, Paul;
Swisher, Elizabeth M.

Publication type:

Article

THE AUTHORS REPLY.

Published in:

American Journal of Epidemiology, 1988, v. 128, n. 1, p. 244, doi. 10.1093/oxfordjournals.aje.a114950

By:

Selby, Joseph V.;
Newman, Beth;
Friedman, Gary D.;
King, Mary-Claire

Publication type:

Article

ENVIRONMENTAL AND BEHAVIORAL DETERMINANTS OF FASTING PLASMA GLUCOSE IN WOMEN.

Published in:

American Journal of Epidemiology, 1987, v. 125, n. 6, p. 979, doi. 10.1093/oxfordjournals.aje.a114636

By:

SELBY, JOSEPH V.;
NEWMAN, BETH;
KING, MARY-CLAIRE;
FRIEDMAN, GARY D.

Publication type:

Article

ONE OF THE AUTHORS REPLIES.

Published in:

American Journal of Epidemiology, 1987, v. 125, n. 5, p. 920, doi. 10.1093/oxfordjournals.aje.a114612

By:

King, Mary-Claire

Publication type:

Article

RISK FACTORS FOR CORONARY HEART DISEASE IN ADULT FEMALE TWINS.

Published in:

American Journal of Epidemiology, 1987, v. 125, n. 2, p. 308, doi. 10.1093/oxfordjournals.aje.a114531

By:

AUSTIN, MELISSA A.;
KING, MARY-CLAIRE;
BAWOL, RICHARD D.;
HULLEY, STEPHEN B.;
FRIEDMAN, GARY D.

Publication type:

Article

FAMILIAL BREAST CANCER IN A POPULATION-BASED SERIES.

Published in:

American Journal of Epidemiology, 1986, v. 123, n. 1, p. 15

By:

OTTMAN, RUTH;
PIKE, MALCOLM C.;
KING, MARY-CLAIRE;
CASAGRANDE, JOHN T.;
HENDERSON, BRIAN E.

Publication type:

Article

Running on screen while black: Representations of black presidential candidates in U.S. film and television.

Published in:

2017

By:

King, Claire Sisco;
Beasley, Vanessa B.

Publication type:

Essay

Rogue Waves, Remakes, and Resurrections: Allegorical Displacement and Screen Memory in Poseidon.

Published in:

Quarterly Journal of Speech, 2008, v. 94, n. 4, p. 430, doi. 10.1080/00335630802422204

By:

King, Claire Sisco

Publication type:

Article

Report on Genetic Epidemiology workshop I, held at Shanghai Medical University, December 24-31, 1988.

Published in:

Genetic Epidemiology, 1990, v. 7, n. 3, p. 231, doi. 10.1002/gepi.1370070307

By:

Shen, Fu Min;
Lee, Ming K.;
King, Mary-Claire;
Rao, D. C.

Publication type:

Article

Genetic epidemiology of persistent islet cell antibodies among IDDM patients.

Published in:

Genetic Epidemiology, 1989, v. 6, n. 1, p. 123, doi. 10.1002/gepi.1370060123

By:

Newman, Beth;
Selby, Joseph;
Lee, Ming;
King, Mary-Claire

Publication type:

Article

Genetic analysis of human breast cancer: Literature review and description of family data in workshop.

Published in:

Genetic Epidemiology, 1986, v. 3, n. S1, p. 1, doi. 10.1002/gepi.1370030704

By:

King, Mary-Claire;
Cannon, Lisa A.;
Bailey-Wilson, Joan E.;
Cleton, F. J.;
DeJong-Bakker, N.;
Gardner, E. J.;
Jacobsen, O.;
King, M-C.;
Lynch, H. T.;
Skolnick, M. H.

Publication type:

Article

Genetic analysis of human breast cancer: A synthesis of contributions to Gaw IV.

Published in:

Genetic Epidemiology, 1986, v. 3, n. S1, p. 15, doi. 10.1002/gepi.1370030705

By:

Bailey-Wilson, Joan E.;
Cannon, Lisa A.;
King, Mary-Claire

Publication type:

Article

TP53 missense allele predisposing to high risk of breast cancer but not pediatric cancers.

Published in:

JNCI: Journal of the National Cancer Institute, 2025, v. 117, n. 5, p. 1069, doi. 10.1093/jnci/djae334

By:

Lolas-Hamameh, Suhair;
Lieberman, Sari;
Sarahneh, Alaa;
Walsh, Tom;
Lee, Ming K;
Gulsuner, Suleyman;
Rabie, Grace;
Beeri, Rachel;
Aburayyan, Amal;
Mandell, Jessica B;
Fridman, Hila;
Lazer-Derbeko, Galit;
Klopstock, Tehila;
Freireich, Orit;
Lahad, Amnon;
King, Mary-Claire;
Levy-Lahad, Ephrat;
Kanaan, Moien N

Publication type:

Article

Precision medicine meets public health: population screening for BRCA1 and BRCA2.

Published in:

2015

By:

Levy-Lahad, Ephrat;
Lahad, Amnon;
King, Mary-Claire

Publication type:

Editorial

Precision Medicine Meets Public Health: Population Screening for BRCA1 and BRCA2.

Published in:

JNCI: Journal of the National Cancer Institute, 2014, v. 107, n. 1, p. 1, doi. 10.1093/jnci/dju420

By:

Levy-Lahad, Ephrat;
Lahad, Amnon;
King, Mary-Claire

Publication type:

Article

Pharmaceutical procurement among public sector procurers in CARICOM.

Published in:

Pan American Journal of Public Health / Revista Panamericana de Salud Pública, 2021, v. 45, p. 1, doi. 10.26633/RPSP.2021.57

By:

Preston, Charles;
King, Claire;
Hinds, Maryam;
Burnett, Francis;
Extavour, Rian Marie

Publication type:

Article

A girl with West syndrome and autistic features harboring a de novo TBL1XR1 mutation.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 10, p. 581, doi. 10.1038/jhg.2014.71

By:

Saitsu, Hirotomo;
Tohyama, Jun;
Walsh, Tom;
Kato, Mitsuhiro;
Kobayashi, Yu;
Lee, Ming;
Tsurusaki, Yoshinori;
Miyake, Noriko;
Goto, Yu-ichi;
Nishino, Ichizo;
Ohtake, Akira;
King, Mary-Claire;
Matsumoto, Naomichi

Publication type:

Article

A paradoxical genotype-phenotype relationship: Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 14, p. 2265, doi. 10.1093/hmg/ddad066

By:

Aburayyan, Amal;
Carlson, Ryan J;
Rabie, Grace N;
Lee, Ming K;
Gulsuner, Suleyman;
Walsh, Tom;
Avraham, Karen B;
Kanaan, Moien N;
King, Mary-Claire

Publication type:

Article

Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE).

Published in:

Human Molecular Genetics, 2019, v. 28, n. 1, p. 133, doi. 10.1093/hmg/ddy334

By:

Seo, Aaron;
Gulsuner, Suleyman;
Pierce, Sarah;
Ben-Harosh, Miri;
Shalev, Hanna;
Walsh, Tom;
Krasnov, Tanya;
Dgany, Orly;
Doulatov, Sergei;
Tamary, Hannah;
Shimamura, Akiko;
King, Mary-Claire

Publication type:

Article

Proposed shift in screening for breast cancer--reply.

Published in:

2015

By:

King, Mary-Claire;
Lahad, Amnon;
Levy-Lahad, Ephrat

Publication type:

commentary

Proposed Shift in Screening for Breast Cancer.

Published in:

2015

By:

King, Mary-Claire;
Lahad, Amnon;
Levy-Lahad, Ephrat

Publication type:

Letter to the Editor

Population-based screening for BRCA1 and BRCA2: 2014 Lasker Award.

Published in:

2014

By:

King, Mary-Claire;
Levy-Lahad, Ephrat;
Lahad, Amnon

Publication type:

journal article

Population-Based Screening for BRCA1 and BRCA2.

Published in:

JAMA: Journal of the American Medical Association, 2014, v. 312, n. 11, p. 1091, doi. 10.1001/jama.2014.12483

By:

King, Mary-Claire;
Levy-Lahad, Ephrat;
Lahad, Amnon

Publication type:

Article

Caring for a dying spouse at the end of life: 'It's one of the things you volunteer for when you get married': a qualitative study of the oldest carers' experiences.

Published in:

Age & Ageing, 2016, v. 45, n. 3, p. 421, doi. 10.1093/ageing/afw047

By:

TURNER, MARY;
KING, CLAIRE;
MILLIGAN, CHRISTINE;
THOMAS, CAROL;
BREARLEY, SARAH G.;
SEAMARK, DAVID;
XU WANG;
BLAKE, SUSAN;
PAYNE, SHEILA

Publication type:

Article