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Mary‐Claire King

University of Glasgow

109H-index
475Paper Count
5.2WCitation Count
Published Papers 163
Publication Date
Bio-banding influences talent experts' ratings of psycho-social behaviours during 11 v 11 soccer match-play
err2025-10-01
err0
PREAI
errRobinson, J.; Forsdyke, D.; Arenas, L.; Dawson, Z.; King, M.; Myhill, N.; Towlson, C.; Springham, M.; Walsh, L.; Mallinson-Howard, S. H.; Barrett, S.; Salter, J.
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Differences in physical and technical performance characteristics between 11 v 11 chronological and bio-banded soccer match-play
err2025-09-18
err0
errOAAI
errJ. Salter; D. Forsdyke; L. Arenas; Z. Dawson; M. King; N. Myhill; J. Robinson; C. Towlson; M. Springham; L. Walsh; S. Mallinson-Howard; S. Barrett
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Long-read DNA and cDNA sequencing identify cancer-predisposing deep intronic variation in tumor-suppressor genes
err2024-09-13
err0
PREAI
errGulsuner, Suleyman; Aburayyan, Amal; Mandell, Jessica B.; Lee, Ming K.; Bernier, Greta V.; Norquist, Barbara M.; Pierce, Sarah B.; King, Mary-Claire; Walsh, Tom
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An evolutionary perspective on complex neuropsychiatric disease
errNEURON
IF15
err2024-01-01
err0
errOAAI
errMcclellan, Jon M.; Zoghbi, Anthony W.; Buxbaum, Joseph D.; Cappi, Carolina; Crowley, James J.; Flint, Jonathan; Grice, Dorothy E.; Gulsuner, Suleyman; Iyegbe, Conrad; Jain, Sanjeev; Kuo, Po-Hsiu; Lattig, Maria Claudia; Passos-Bueno, Maria Rita; Purushottam, Meera; Stein, Dan J.; Sunshine, Anna B.; Susser, Ezra S.; Walsh, Christopher A.; Wootton, Olivia; King, Mary-Claire
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A paradoxical genotype-phenotype relationship: Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss
err2023-04-19
err0
errOAAI
errAburayyan, Amal; Carlson, Ryan J.; Rabie, Grace N.; Lee, Ming K.; Gulsuner, Suleyman; Walsh, Tom; Avraham, Karen B.; Kanaan, Moien N.; King, Mary-Claire
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Association of Genetic Diagnoses of Childhood-Onset Hearing Loss With Cochlear Implant Outcomes
err2023-03-01
err20
errOAAI
errCarlson, Ryan J.; Walsh, Tom; Mandell, Jessica B.; Aburayyan, Amal; Lee, Ming K.; Gulsuner, Suleyman; Horn, David L.; Ou, Henry C.; Sie, Kathleen C. Y.; Mancl, Lisa; Rubinstein, Jay; King, Mary-Claire
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Clinically Complex LRBA Deficiency Due to a Founder Allele in the Georgian Jewish Population
err2022-09-05
err1
PREAI
errFreund, Tal; Baxter, Sarah K.; Walsh, Tom; Golan, Hana; Kapelushnik, Joseph; Abramsohn-Goldenberg, Michal; Benor, Shira; Sarid, Nadav; Ram, Ron; Alcalay, Yifat; Segel, Reeval; Renbaum, Paul; Stepensky, Polina; King, Mary-Claire; Torgerson, Troy R.; Hagin, David
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Mutational spectrum of breast cancer susceptibility genes among women ascertained in a cancer risk clinic in Northeast Brazil
err2022-03-30
err11
errOAAI
errFelix, Gabriela E. S.; Guindalini, Rodrigo Santa Cruz; Zheng, Yonglan; Walsh, Tom; Sveen, Elisabeth; Machado Lopes, Taisa Manuela; Cortes, Juliana; Zhang, Jing; Carozo, Polyanna; Santos, Irlania; Bonfim, Thais Ferreira; Garicochea, Bernardo; Pereira Toralles, Maria Betania; Meyer, Roberto; Netto, Eduardo Martins; Abe-Sandes, Kiyoko; King, Mary-Claire; de Oliveira Nascimento, Ivana Lucia; Olopade, Olufunmilayo, I
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Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy, and enteropathy, and implications for clinical management
err2022-01-01
err21
errOAAI
errBaxter, Sarah K.; Walsh, Tom; Casadei, Silvia; Eckert, Mary M.; Allenspach, Eric J.; Hagin, David; Segundo, Gesmar; Lee, Ming K.; Gulsuner, Suleyman; Shirts, Brian H.; Sullivan, Kathleen E.; Keller, Michael D.; Torgerson, Troy R.; King, Mary-Claire
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Adaptation and Validation of a Computerized Neurocognitive Battery in the Xhosa of South Africa
err2021-09-01
err7
errOAAI
errScott, J. Cobb; Moore, Tyler M.; Stein, Dan J.; Pretorius, Adele; Zingela, Zukiswa; Nagdee, Mohammed; Ngqengelele, Linda; Campbell, Megan; Sibeko, Goodman; King, Mary Claire; McClellan, Jon M.; Port, Allison M.; Jackson, Chad; Ruparel, Kosha; Susser, Ezra S.; Gur, Ruben C.
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Targeted long-read sequencing identifies missing disease-causing variation
err2021-08-01
err137
errOAAI
errMiller, Danny E.; Sulovari, Arvis; Wang, Tianyun; Loucks, Hailey; Hoekzema, Kendra; Munson, Katherine M.; Lewis, Alexandra P.; Fuerte, Edith P. Almanza; Paschal, Catherine R.; Walsh, Tom; Thies, Jenny; Bennett, James T.; Glass, Ian; Dipple, Katrina M.; Patterson, Karynne; Bonkowski, Emily S.; Nelson, Zoe; Squire, Audrey; Sikes, Megan; Beckman, Erika; Bennett, Robin L.; Earl, Dawn; Lee, Winston; Allikmets, Rando; Perlman, Seth J.; Chow, Penny; Hing, Anne, V; Wenger, Tara L.; Adam, Margaret P.; Sun, Angela; Lam, Christina; Chang, Irene; Zou, Xue; Austin, Stephanie L.; Huggins, Erin; Safi, Alexias; Iyengar, Apoorva K.; Reddy, Timothy E.; Majoros, William H.; Allen, Andrew S.; Crawford, Gregory E.; Kishnani, Priya S.; King, Mary-Claire; Cherry, Tim; Chong, Jessica X.; Bamshad, Michael J.; Nickerson, Deborah A.; Mefford, Heather C.; Doherty, Dan; Eichler, Evan E.
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Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsy
err2021-07-28
err20
PREAI
errYechieli, Michal; Gulsuner, Suleyman; Ben-Pazi, Hilla; Fattal, Aviva; Aran, Adi; Kuzminsky, Alla; Sagi, Liora; Guttman, Dafna; Schneebaum Sender, Nira; Gross-Tsur, Varda; Klopstock, Tehila; Walsh, Tom; Renbaum, Paul; Zeligson, Sharon; Shemer Meiri, Lilach; Lev, Dorit; Shmueli, Dorit; Blumkin, Luba; Lahad, Amnon; King, Mary-Claire; Levy, Ephrat Lahad; Segel, Reeval
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A tipping point in neuropsychiatric genetics
errNEURON
IF15
err2021-05-01
err3
errOAAI
errMcClellan, Jon M.; King, Mary -Claire
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Cisplatin +/- rucaparib after preoperative chemotherapy in patients with triple-negative or BRCA mutated breast cancer
err2021-03-22
err20
errOAAI
errKalra, Maitri; Tong, Yan; Jones, David R.; Walsh, Tom; Danso, Michael A.; Ma, Cynthia X.; Silverman, Paula; King, Mary-Claire; Badve, Sunil S.; Perkins, Susan M.; Miller, Kathy D.
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Germline variants drive myelodysplastic syndrome in young adults
errLEUKEMIA
IF13.4
err2021-01-28
err47
errOAAI
errFeurstein, Simone; Churpek, Jane E.; Walsh, Tom; Keel, Sioban; Hakkarainen, Marja; Schroeder, Thomas; Germing, Ulrich; Geyh, Stefanie; Heuser, Michael; Thol, Felicitas; Pohlkamp, Christian; Haferlach, Torsten; Gao, Juehua; Owen, Carolyn; Goehring, Gudrun; Schlegelberger, Brigitte; Verma, Divij; Krause, Daniela S.; Gao, Guimin; Cronin, Tara; Gulsuner, Suleyman; Lee, Ming; Pritchard, Colin C.; Subramanian, Hari Prasanna; del Gaudio, Daniela; Li, Zejuan; Das, Soma; Kilpivaara, Outi; Wartiovaara-Kautto, Ulla; Wang, Eunice S.; Griffiths, Elizabeth A.; Dohner, Konstanze; Dohner, Hartmut; King, Mary-Claire; Godley, Lucy A.
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Inherited predisposition to breast cancer in the Carolina Breast Cancer Study
err2021-01-21
err12
errOAAI
errWalsh, Tom; Gulsuner, Suleyman; Lee, Ming K.; Troester, Melissa A.; Olshan, Andrew F.; Earp, H. Shelton; Perou, Charles M.; King, Mary-Claire
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Hiding in Plain Sight - Somatic Mutation in Human Disease
err2020-12-31
err15
PREAI
errLevy-Lahad, Ephrat; King, Mary-Claire
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CRISPR-Cas9/long-read sequencing approach to identify cryptic mutations in BRCA1 and other tumour suppressor genes
err2020-10-15
err27
errOAAI
errWalsh, Tom; Casadei, Silvia; Munson, Katherine M.; Eng, Mary; Mandell, Jessica B.; Gulsuner, Suleyman; King, Mary-Claire
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Telomere biology disorder prevalence and phenotypes in adults with familial hematologic and/or pulmonary presentations
err2020-10-09
err26
errOAAI
errFeurstein, Simone; Adegunsoye, Ayodeji; Mojsilovic, Danijela; Vij, Rekha; DePersia, Allison H. West; Rajagopal, Padma Sheila; Osman, Afaf; Collins, Robert H.; Kim, Raymond H.; Gore, Steven D.; Greenberg, Peter; Godley, Lucy A.; Li, Zejuan; del Gaudio, Daniela; Subramanian, Hari Prasanna; Das, Soma; Walsh, Tom; Gulsuner, Suleyman; Segal, Jeremy P.; Husain, Aliya N.; Gurbuxani, Sandeep; King, Mary-Claire; Strek, Mary E.; Churpek, Jane E.
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