J. McClellan
Genetics · Science · 2007–2010
A researcher in the Science corpus: 5 papers; trusts 3 researchers and is trusted by 3 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 50 citations into it; #3,151 of 6,854 by trust here, #854 by citations
- Cognitive Neuroscience — 20 citations into it
Whom J. McClellan trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- L. Weiss
- J. K. Pritchard
- M. Nachman
- Edwin H. Cook Jr.
- David B. Goldstein
- Dennis S. Charney
- Dan E. Arking
- Kai Wang
Who trusts J. McClellan overall
- Jay N. Giedd
- Judith L. Rapoport
- L. Yatham
- Melissa S. Cline
- Rudolph E. Tanzi
- Thomas R. Insel
- Lars Bertram
Papers from J. McClellan's perspective
Ordered by how strongly the researchers J. McClellan trusts endorse each paper. Same corpus, a different order for every researcher.
- Principal components analysis corrects for stratification in genome-wide association studies
- Disruption of two novel genes by a translocation co-segregating with schizophrenia. (Human Molecular Genetics)
- PLINK: a tool set for whole-genome association and population-based linkage analyses.
- Integrated detection and population-genetic analysis of SNPs and copy number variation (Nature Genetics)
- Strong Association of De Novo Copy Number Mutations with Autism (Science)
- Common genetic variants on 5p14.1 associate with autism spectrum disorders (Nature)
- Strong association of de novo copy number mutations with sporadic schizophrenia (Nature Genetics)
- Defining clinical phenotypes of juvenile mania. (American Journal of Psychiatry)
- The prevalence and disability of bipolar spectrum disorders in the US population: re-analysis of the ECA database taking into account subthreshold cases. (Journal of Affective Disorders)
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes (Nature)
Their papers
- Microduplications of 16p11.2 are Associated with Schizophrenia (2009) — 730 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
- Practice parameter for the assessment and treatment of children and adolescents with bipolar disorder. (2007) — 620 citations