Shrikant M. Mane

Molecular Biology · 2002–2019

A researcher in the Science corpus: 22 papers; trusts 4 researchers and is trusted by 16 researchers here, as inferred from the citation graph.

Subfields

Molecular Biology — 260 citations into it; #3,554 of 17,773 by trust here, #1,948 by citations
Genetics — 240 citations into it
Artificial Intelligence — 15 citations into it

Whom Shrikant M. Mane trusts overall

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

Who trusts Shrikant M. Mane overall

Papers from Shrikant M. Mane's perspective

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

Generalized Linear Models
Genome sequencing in microfabricated high-density picolitre reactors (Nature)
Linear Models and Empirical Bayes Methods for Assessing Differential Expression in Microarray Experiments (Statistical Applications in Genetics and Molecular Biology)
Normalization of cDNA microarray data. (Methods)
Moderated statistical tests for assessing differences in tag abundance (Bioinform.)
Statistical significance for genomewide studies (Proceedings of the National Academy of Sciences of the United States of America)
Systematic variation in gene expression patterns in human cancer cell lines (Nature Genetics)
DAVID: Database for Annotation, Visualization, and Integrated Discovery (Genome Biology)
Mapping short DNA sequencing reads and calling variants using mapping quality scores. (Genome Research)
The MicroArray Quality Control (MAQC) project shows inter- and intraplatform reproducibility of gene expression measurements (Nature Biotechnology)

Their papers

RNA-seq: an assessment of technical reproducibility and comparison with gene expression arrays. (2008) — 2,942 citations
Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma (2012) — 1,151 citations
A Novel miRNA Processing Pathway Independent of Dicer Requires Argonaute2 Catalytic Activity (2010) — 901 citations
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011) — 1,286 citations
Functional and Evolutionary Insights Into Human Brain Development Through Global Transcriptome Analysis (2009) — 606 citations
De novo mutations in histone modifying genes in congenital heart disease (2013) — 900 citations
Mutations in Kelch-like 3 and Cullin 3 cause hypertension and electrolyte abnormalities (2012) — 605 citations
K+ Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension (2011) — 959 citations
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands (2017) — 773 citations
Insights into genetics, human biology and disease gleaned from family based genomic studies (2019) — 179 citations
Analysis of shared heritability in common disorders of the brain (2018) — 1,836 citations
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci (2015) — 1,391 citations
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities. (2015) — 611 citations
De novo mutations in Congenital Heart Disease with Neurodevelopmental and Other Birth Defects (2015) — 730 citations
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) — 750 citations
The contribution of de novo coding mutations to autism spectrum disorder (2014) — 2,476 citations
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism (2013) — 905 citations
Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMO (2013) — 832 citations
De novo mutations revealed by whole-exome sequencing are strongly associated with autism (2012) — 2,079 citations
Genome-wide association study identifies susceptibility loci for IgA nephropathy (2011) — 623 citations