M. King

Genetics · Science · 2001–2016

A researcher in the Science corpus: 15 papers; trusts 3 researchers and is trusted by 4 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 107 citations into it; #2,757 of 6,854 by trust here, #292 by citations
• Cognitive Neuroscience — 20 citations into it

Whom M. King trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. L. Weiss

Who trusts M. King overall

1. Jay N. Giedd
2. Judith L. Rapoport
3. Avshalom Caspi
4. M. Kastan

Papers from M. King's perspective

Ordered by how strongly the researchers M. King trusts endorse each paper. Same corpus, a different order for every researcher.

1. Principal components analysis corrects for stratification in genome-wide association studies
2. Association between microdeletion and microduplication at 16p11.2 and autism. (New England Journal of Medicine)
3. Large recurrent microdeletions associated with schizophrenia (Nature)
4. Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer. (American Journal of Human Genetics)
5. PLINK: a tool set for whole-genome association and population-based linkage analyses.
6. Strong Association of De Novo Copy Number Mutations with Autism (Science)
7. Disruption of two novel genes by a translocation co-segregating with schizophrenia. (Human Molecular Genetics)
8. Integrated detection and population-genetic analysis of SNPs and copy number variation (Nature Genetics)
9. Common genetic variants on 5p14.1 associate with autism spectrum disorders (Nature)
10. Copy Number Variation in Human Health, Disease, and Evolution (Annual review of genomics and human genetics (Print))

Their papers

• Initial sequence of the chimpanzee genome and comparison with the human genome (2005) — 2,343 citations
• A recurrent 16p12.1 microdeletion suggests a two-hit model for severe developmental delay (2010) — 596 citations
• Microduplications of 16p11.2 are Associated with Schizophrenia (2009) — 730 citations
• BRCA1 and BRCA2 and the genetics of breast and ovarian cancer. (2001) — 677 citations
• Inherited Mutations in Women with Ovarian Carcinoma (2016) — 698 citations
• Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy. (2014) — 613 citations
• Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas (2013) — 928 citations
• Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing (2011) — 918 citations
• Genetic heterogeneity in human disease. (2010) — 1,010 citations
• Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes (2008) — 695 citations
• Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia (2008) — 1,770 citations
• Strong Association of De Novo Copy Number Mutations with Autism (2007) — 2,845 citations
• Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer. (2006) — 757 citations
• Breast and Ovarian Cancer Risks Due to Inherited Mutations in BRCA1 and BRCA2 (2003) — 2,115 citations
• 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) — 781 citations