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Author Details
Full Name
Praveen F Cherukuri
Affiliation
Sanford School of Medicine, University of South Dakota
ORCID
Career Start Year
2005
Papers
29
H Index
21
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35287663
Establishing analytical validity of BeadChip array genotype data by comparison to whole-genome sequence and standard benchmark datasets.
BMC Med Genomics
2022
35946377
Can tandem alternative splicing and evasion of premature termination codon surveillance contribute to attenuated Peutz-Jeghers syndrome?
Am J Med Genet A
2022
31730267
Pan-cancer RNA-seq data stratifies tumours by some hallmarks of cancer.
J Cell Mol Med
2020
27179618
Complex translocation disrupting TCF4 and altering TCF4 isoform expression segregates as mild autosomal dominant intellectual disability.
Orphanet J Rare Dis
2016
26602380
Replicate exome-sequencing in a multiple-generation family: improved interpretation of next-generation sequencing data.
BMC Genomics
2015
24628908
Identification of candidate genes involved in coronary artery calcification by transcriptome sequencing of cell lines.
BMC Genomics
2014
24603370
Gene-based sequencing identifies lipid-influencing variants with ethnicity-specific effects in African Americans.
PLoS Genet
2014
23292442
Reproduction and immunity-driven natural selection in the human WFDC locus.
Mol Biol Evol
2013
24356879
Sequence diversity of Pan troglodytes subspecies and the impact of WFDC6 selective constraints in reproductive immunity.
Genome Biol Evol
2013
23755103
Sequencing of candidate chromosome instability genes in endometrial cancers reveals somatic mutations in ESCO1, CHTF18, and MRE11A.
PLoS One
2013
23453856
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).
Neuromuscul Disord
2013
22146942
Exome sequencing and SNP analysis detect novel compound heterozygosity in fatty acid hydroxylase-associated neurodegeneration.
Eur J Hum Genet
2012
22864914
Circadian changes in long noncoding RNAs in the pineal gland.
Proc Natl Acad Sci U S A
2012
22585771
Incidental medical information in whole-exome sequencing.
Pediatrics
2012
22675082
Exome sequencing as a diagnostic tool in a case of undiagnosed juvenile-onset GM1-gangliosidosis.
Neurology
2012
22311686
An analysis of exome sequencing for diagnostic testing of the genes associated with muscle disease and spastic paraplegia.
Hum Mutat
2012
21258341
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum.
Nat Genet
2011
22022284
Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases.
PLoS Genet
2011
21767969
Personalized genomic medicine: lessons from the exome.
Mol Genet Metab
2011
21946352
Exon capture analysis of G protein-coupled receptors identifies activating mutations in GRM3 in melanoma.
Nat Genet
2011
21901109
Predisposition to cancer caused by genetic and functional defects of mammalian Atad5.
PLoS Genet
2011
21900194
Genome-wide ChIP-Seq reveals a dramatic shift in the binding of the transcription factor erythroid Kruppel-like factor during erythrocyte differentiation.
Blood
2011
20451169
Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate.
Am J Hum Genet
2010
20709904
Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p.
Blood
2010
20920668
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy.
Am J Hum Genet
2010
19602640
The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine.
Genome Res
2009
17357158
Predicting protein domain interactions from coevolution of conserved regions.
Proteins
2007
16949097
Co-evolutionary analysis of domains in interacting proteins reveals insights into domain-domain interactions mediating protein-protein interactions.
J Mol Biol
2006
15608175
CDD: a Conserved Domain Database for protein classification.
Nucleic Acids Res
2005
1 - 29 of 29
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National Human Genome Research Institute, National Institutes of Health
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