King, Mary-Claire

Evolution at Two Levels in Humans and Chimpanzees: Their macromolecules are so alike that regulatory mutations may account for their biological differences

King, M.-C., & Wilson, A. C. (1975) · Science

Pleistocene-Era Hominins and ArchaeologyEvolution and Genetic Dynamics

Cited by 2,815

Strong association of de novo copy number mutations with autism

Sebat, J., Lakshmi, B., Malhotra, D., Troge, J., Lese-Martin, C., Walsh, T., Yamrom, B., Yoon, S., Krasnitz, A., Kendall, J., et al. (2007) · Science

Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research

Cited by 2,795

Breast and Ovarian Cancer Risks Due to Inherited Mutations in BRCA1 and BRCA2

King, M.-C., Marks, J. H., & Mandell, J. B. (2003) · Science

BRCA gene mutations in cancerMultiple and Secondary Primary Cancers

Cited by 2,229

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

Walsh, T., McClellan, J. M., McCarthy, S. E., Addington, A. M., Pierce, S. B., Cooper, G. M., Nord, A. S., Kusenda, M., Malhotra, D., Bhandari, A., et al. (2008) · Science

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 1,800

Atherogenic lipoprotein phenotype. A proposed genetic marker for coronary heart disease risk

Austin, M. A., King, M. C., Vranizan, K. M., & Krauss, R. M. (1990) · Circulation

Lipoproteins and Cardiovascular HealthLipid metabolism and disorders

Cited by 1,411

Genetic Heterogeneity in Human Disease

McClellan, J., & King, M.-C. (2010) · Cell

Genomics and Rare DiseasesGenetic Associations and Epidemiology

Cited by 981

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

Mefford, H. C., Sharp, A. J., Baker, C., Itsara, A., Jiang, Z., Buysse, K., Huang, S., Maloney, V. K., Crolla, J. A., Baralle, D., et al. (2008) · New England Journal of Medicine

Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms

Cited by 804

Microduplications of 16p11.2 are associated with schizophrenia

Wellcome Trust Case Control Consortium, McCarthy, S. E., Makarov, V., Kirov, G., Addington, A. M., McClellan, J., Yoon, S., Perkins, D. O., Dickel, D. E., Kusenda, M., et al. (2009) · Nature Genetics

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 711

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

Girirajan, S., Rosenfeld, J. A., Cooper, G. M., Antonacci, F., Siswara, P., Itsara, A., Vives, L., Walsh, T., McCarthy, S. E., Baker, C., et al. (2010) · Nature Genetics

Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms

Cited by 667

Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network

Gulsuner, S., Walsh, T., Watts, A. C., Lee, M. K., Thornton, A. M., Casadei, S., Rippey, C., Shahin, H., Braff, D., Cadenhead, K. S., et al. (2013) · Cell

Schizophrenia research and treatmentGenomic variations and chromosomal abnormalities

Cited by 536

Ten Genes for Inherited Breast Cancer

Walsh, T., & King, M.-C. (2007) · Cancer Cell

BRCA gene mutations in cancerBreast Lesions and Carcinomas

Cited by 477

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

Vacic, V., McCarthy, S., Malhotra, D., Murray, F., Chou, H.-H., Peoples, A., Makarov, V., Yoon, S., Bhandari, A., Corominas, R., et al. (2011) · Nature

Schizophrenia research and treatmentGenomic variations and chromosomal abnormalities

Cited by 337

Schizophrenia: a common disease caused by multiple rare alleles

McClellan, J. M., Susser, E., & King, M.-C. (2007) · British Journal of Psychiatry

Schizophrenia research and treatmentGenetic Associations and Epidemiology

Cited by 296

Genetics of schizophrenia in the South African Xhosa

Gulsuner, S., Stein, D. J., Susser, E. S., Sibeko, G., Pretorius, A., Walsh, T., Majara, L., Mndini, M. M., Mqulwana, S. G., Ntola, O. A., et al. (2020) · Science

Schizophrenia research and treatmentGenetic Associations and Epidemiology

Cited by 118

Genomic Analysis of Mental Illness: A Changing Landscape

McClellan, J., & King, M.-C. (2010) · JAMA

Schizophrenia research and treatmentGenetic Associations and Epidemiology

Cited by 63

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

Saitsu, H., Tohyama, J., Walsh, T., Kato, M., Kobayashi, Y., Lee, M., Tsurusaki, Y., Miyake, N., Goto, Y.-I., Nishino, I., et al. (2014) · Journal of Human Genetics

Genetics and Neurodevelopmental DisordersEpilepsy research and treatment

Cited by 57