P. Cherukuri

发表

Co-evolutionary analysis of domains in interacting proteins reveals insights into domain-domain interactions mediating protein-protein interactions.

Raja Jothi, T. Przytycka, A. Tasneem, 2006, Journal of molecular biology.

Research in Genomic Medicine the Clinseq Project: Piloting Large-scale Genome Sequencing for Material Supplemental

Alexander F. Wilson, A. F. Wilson, J. Mullikin, 2009 .

Gene-Based Sequencing Identifies Lipid-Influencing Variants with Ethnicity-Specific Effects in African Americans

C. Rotimi, A. Adeyemo, J. Mullikin, 2014, PLoS genetics.

Predicting protein domain interactions from coevolution of conserved regions

Teresa M Przytycka, Maricel G Kann, Raja Jothi, 2007, Proteins.

An analysis of exome sequencing for diagnostic testing of the genes associated with muscle disease and spastic paraplegia

Yan Huang, Murat Sincan, William A Gahl, 2012, Human mutation.

Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate.

Jamie K Teer, Leslie G Biesecker, James C Mullikin, 2010, American journal of human genetics.

Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)

K. F. Fajardo, J. Mullikin, M. Sincan, 2013, Neuromuscular Disorders.

Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy.

Nancy F. Hansen, J. Lupski, J. Mullikin, 2010, American journal of human genetics.

Complex translocation disrupting TCF4 and altering TCF4 isoform expression segregates as mild autosomal dominant intellectual disability

Barbara N. Pusey, P. Stankiewicz, J. Mullikin, 2016, Orphanet Journal of Rare Diseases.

Can tandem alternative splicing and evasion of premature termination codon surveillance contribute to attenuated Peutz–Jeghers syndrome?

Phillip A. Richmond, C. Boerkoel, P. Cherukuri, 2022, American journal of medical genetics. Part A.

locus assignment to chromosome 3p Gray platelet syndrome: natural history of a large patient cohort and

J. Mullikin, N. Hansen, D. Geiger, 2011 .

Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p.

J. Mullikin, N. Hansen, D. Geiger, 2010, Blood.

Identification of candidate genes involved in coronary artery calcification by transcriptome sequencing of cell lines

Larry N. Singh, J. Mullikin, E. Green, 2014, BMC Genomics.

Personalized genomic medicine: lessons from the exome.

Nancy F. Hansen, J. Mullikin, N. Hansen, 2011, Molecular genetics and metabolism.

Pan‐cancer RNA‐seq data stratifies tumours by some hallmarks of cancer

C. Boerkoel, P. Cherukuri, F. G. Frost, 2019, Journal of cellular and molecular medicine.

CDD: a Conserved Domain Database for protein classification

John B. Anderson, Benjamin A. Shoemaker, Dachuan Zhang, 2004, Nucleic Acids Res..

Predisposition to Cancer Caused by Genetic and Functional Defects of Mammalian Atad5

Nancy F. Hansen, Lana M. Pollock, T. Wolfsberg, 2011, PLoS genetics.

Sequence Diversity of Pan troglodytes Subspecies and the Impact of WFDC6 Selective Constraints in Reproductive Immunity

Warren W. Kretzschmar, S. Tishkoff, A. Clark, 2013, Genome biology and evolution.

Incidental Medical Information in Whole-Exome Sequencing

J. Mullikin, N. Hansen, D. Pineda-Alvarez, 2012, Pediatrics.

Exon capture analysis of G protein-coupled receptors identifies activating mutations in GRM3 in melanoma

E. H. Margulies, Jimmy Lin, Xiaomu Wei, 2011, Nature Genetics.

TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum

Colin A. Johnson, Nancy F. Hansen, R. Gibbs, 2011, Nature Genetics.

Sequencing of Candidate Chromosome Instability Genes in Endometrial Cancers Reveals Somatic Mutations in ESCO1, CHTF18, and MRE11A

Nancy F. Hansen, Lana M. Pollock, J. Mullikin, 2013, PloS one.

Replicate exome-sequencing in a multiple-generation family: improved interpretation of next-generation sequencing data

J. Mullikin, V. Maduro, D. Adams, 2015, BMC Genomics.

Genome-wide ChIP-Seq reveals a dramatic shift in the binding of the transcription factor erythroid Kruppel-like factor during erythrocyte differentiation.

S. S. Ajay, E. H. Margulies, J. Mullikin, 2011, Blood.

Circadian changes in long noncoding RNAs in the pineal gland

J. Mullikin, P. Munson, P. Cherukuri, 2012, Proceedings of the National Academy of Sciences.

Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases

Anthony Sandler, Nancy F. Hansen, Jamie K. Teer, 2011, PLoS genetics.

Correction: Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases

J. Mullikin, E. Rugarli, N. Hansen, 2013, PLoS Genetics.

Exome sequencing as a diagnostic tool in a case of undiagnosed juvenile-onset GM1-gangliosidosis

Nancy F. Hansen, J. Mullikin, N. Hansen, 2012, Neurology.

gangliosidosis 1 juvenile-onset GM Exome sequencing as a diagnostic tool in a case of undiagnosed

Nancy F. Hansen, K. F. Fajardo, J. Mullikin, 2012 .

Establishing analytical validity of BeadChip array genotype data by comparison to whole-genome sequence and standard benchmark datasets

Cornelius F. Boerkoel, Lynn K. Carmichael, Catherine Hajek, 2021, BMC medical genomics.

Reproduction and immunity-driven natural selection in the human WFDC locus.

Eric D Green, James C Mullikin, Pedro Cruz, 2013, Molecular biology and evolution.

Exome sequencing and SNP analysis detect novel compound heterozygosity in fatty acid hydroxylase-associated neurodegeneration

Murat Sincan, William A Gahl, Pedro Cruz, 2011, European Journal of Human Genetics.

Replicate exome-sequencing in a multiple-generation family: improved interpretation of next-generation sequencing data

J. Mullikin, V. Maduro, D. Adams, 2015, BMC Genomics.

Identification of candidate genes involved in coronary artery calcification by transcriptome sequencing of cell lines

Larry N. Singh, J. Mullikin, E. Green, 2014, BMC Genomics.

The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine.

Nancy F. Hansen, Alexander F. Wilson, J. Mullikin, 2009, Genome research.

Identification of candidate genes involved in coronary artery calcification by transcriptome sequencing of cell lines

Larry N. Singh, J. Mullikin, E. Green, 2014, BMC Genomics.

Systematic Identification and Definition of Consistently Well-Characterized Protein-Coding Exons Using Next Generation Sequencing Technology

K. F. Fajardo, M. Sincan, C. Boerkoel, 2013 .