Praveen F. Cherukuri

ScholarGPS® ID: 88005317230708

Affiliation
University of South Dakota, Vermillion, United States
Affiliation History

Field
Life Sciences
Discipline
Genetics
Top Specialties
Exome Sequencing | Mutation | Genomics
Metrics Summary
Publication Count
25
Predicted Citations
1,977
Predicted h-index
21
Ranking

Publications and Citation History

Publications based on Top Specialties

Types of Publication

  • Publications
  • Books
  • Patents
  • NIH/NSF
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Can tandem alternative splicing and evasion of premature termination codon surveillance contribute to attenuated Peutz–Jeghers syndrome? (journal article)
Gazzaz, Nour | Frost, F. Graeme | Alderman, Emily | Richmond, Phillip A. | Dalmann, Joshua | Lin, Susan | Salman, Areesha | Del Bel, Kate L. | Lehman, Anna | Turvey, Stuart E. | ... | Cherukuri, Praveen F.
American Journal of Medical Genetics Part A, volume 188, issue 10, pages 3089-3095 (2022).
10.1002/ajmg.a.62942
Cited by (3) | Cite | Source
Establishing analytical validity of BeadChip array genotype data by comparison to whole-genome sequence and standard benchmark datasets (journal article)
Cherukuri, Praveen F. | Soe, Melissa M. | Condon, David E. | Bartaria, Shubhi | Meis, Kaitlynn | Gu, Shaopeng | Frost, Frederick G. | Fricke, Lindsay M. | Lubieniecki, Krzysztof P. | Lubieniecka, Joanna M. | ... | Carmichael, Lynn
BMC Medical Genomics, volume 15, issue 1 (2022).
10.1186/s12920-022-01199-8
Cited by (2) | Cite | Source
Pan‐cancer RNA‐seq data stratifies tumours by some hallmarks of cancer (journal article)
Frost, F. Graeme | Cherukuri, Praveen F. | Milanovich, Samuel | Boerkoel, Cornelius F.
Journal of Cellular and Molecular Medicine, volume 24, issue 1, pages 418-430 (2020).
10.1111/jcmm.14746
Cited by (23) | Cite | Source
Complex translocation disrupting TCF4 and altering TCF4 isoform expression segregates as mild autosomal dominant intellectual disability (journal article)
Maduro, Valerie | Pusey, Barbara N. | Cherukuri, Praveen F. | Atkins, Paul | du Souich, Christèle | Rupps, Rosemarie | Limbos, Marjolaine | Adams, David R. | Bhatt, Samarth S. | Eydoux, Patrice | ... | Boerkoel, Cornelius F.
Orphanet Journal of Rare Diseases, volume 11, issue 1 (2016).
10.1186/s13023-016-0439-6
Cited by (24) | Cite | Source | Open Access
Replicate exome-sequencing in a multiple-generation family: improved interpretation of next-generation sequencing data (journal article)
Cherukuri, Praveen F. | Maduro, Valerie | Fuentes-Fajardo, Karin V. | Lam, Kevin | Adams, David R. | Tifft, Cynthia J. | Mullikin, James C. | Gahl, William A. | Boerkoel, Cornelius F.
BMC Genomics, volume 16, issue 1 (2015).
10.1186/s12864-015-2107-y
Cited by (7) | Cite | Source | Open Access
Identification of candidate genes involved in coronary artery calcification by transcriptome sequencing of cell lines (journal article)
Sen, Shurjo K | Barb, Jennifer J | Cherukuri, Praveen F | Accame, David S | Elkahloun, Abdel G | Singh, Larry N | Lee-Lin, Shih-Queen | Program, NISC Comparative Sequencing | Kolodgie, Frank D | Cheng, Qi | ... | Biesecker, Leslie G
BMC Genomics, volume 15, issue 1 (2014).
10.1186/1471-2164-15-198
Cited by (12) | Cite | Source | Open Access
Gene-Based Sequencing Identifies Lipid-Influencing Variants with Ethnicity-Specific Effects in African Americans (journal article)
Bentley, Amy R. | Chen, Guanjie | Shriner, Daniel | Doumatey, Ayo P. | Zhou, Jie | Huang, Hanxia | Mullikin, James C. | Blakesley, Robert W. | Hansen, Nancy F. | Bouffard, Gerard G. | ... | Rotimi, Charles N.
PLoS Genetics, volume 10, issue 3, pages e1004190- (2014).
10.1371/journal.pgen.1004190
Cited by (29) | Cite | Source | Open Access
Sequence Diversity of Pan troglodytes Subspecies and the Impact of WFDC6 Selective Constraints in Reproductive Immunity (journal article)
Ferreira, Zélia | Hurle, Belen | Andrés, Aida M. | Kretzschmar, Warren W. | Mullikin, James C. | Cherukuri, Praveen F. | Cruz, Pedro | Gonder, Mary Katherine | Stone, Anne C. | Tishkoff, Sarah | ... | Seixas, Susana
Genome Biology and Evolution, volume 5, issue 12, pages 2512-2523 (2013).
10.1093/gbe/evt198
Cited by (1) | Cite | Source | Open Access
Sequencing of Candidate Chromosome Instability Genes in Endometrial Cancers Reveals Somatic Mutations in ESCO1, CHTF18, and MRE11A (journal article)
Price, Jessica C. | Pollock, Lana M. | Rudd, Meghan L. | Fogoros, Sarah K. | Mohamed, Hassan | Hanigan, Christin L. | Le Gallo, Matthieu | Zhang, Suiyuan | Cruz, Pedro | Cherukuri, Praveen F. | ... | Bell, Daphne W.
PLoS ONE, volume 8, issue 6, pages e63313- (2013).
10.1371/journal.pone.0063313
Cited by (24) | Cite | Source | Open Access
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) (journal article)
Pierson, Tyler Mark | Markello, Thomas | Accardi, John | Wolfe, Lynne | Adams, David | Sincan, Murat | Tarazi, Noor M. | Fajardo, Karin Fuentes | Cherukuri, Praveen F. | Bajraktari, Ilda | ... | Tifft, Cynthia J.
Neuromuscular Disorders, volume 23, issue 6, pages 483-488 (2013).
10.1016/j.nmd.2013.01.013
Cited by (21) | Cite | Source | Open Access
Reproduction and Immunity-Driven Natural Selection in the Human WFDC Locus (journal article)
Ferreira, Zélia | Seixas, Susana | Andrés, Aida M. | Kretzschmar, Warren W. | Mullikin, James C. | Cherukuri, Praveen F. | Cruz, Pedro | Swanson, Willie J. | Clark, Andrew G. | Green, Eric D. | Hurle, Belen
Molecular Biology and Evolution, volume 30, issue 4, pages 938-950 (2013).
10.1093/molbev/mss329
Cited by (17) | Cite | Source | Open Access
G.P.95 Two sibs with early onset myopathy with areflexia, respiratory distress, and dysphagia (EMARDD) due to homozygous exon 7 deletion in MEGF10 (journal article)
Meilleur, K.G. | Pierson, T.M. | Jain, M. | Donkervoort, S. | Markello, T. | Wolfe, L. | Accardi, J. | Adams, D. | Sincan, M. | Fuentes-Fajardo, K. | ... | Bonnemann, C.G.
Neuromuscular Disorders, volume 22, issue 9-10, pages 870-871 (2012).
10.1016/j.nmd.2012.06.225
Cite | Source
Exome sequencing as a diagnostic tool in a case of undiagnosed juvenile-onset GM1 -gangliosidosis (journal article)
Pierson, Tyler Mark | Adams, David A. | Markello, Thomas | Golas, Gretchen | Yang, Sandra | Sincan, Murat | Simeonov, Dimitre R. | Fuentes Fajardo, Karin | Hansen, Nancy F. | Cherukuri, Praveen F. | ... | Tifft, Cynthia J.
Neurology, volume 79, issue 2, pages 123-126 (2012).
10.1212/WNL.0b013e31825f047a
Cited by (32) | Cite | Source | Open Access
Incidental Medical Information in Whole-Exome Sequencing (journal article)
Solomon, Benjamin D. | Hadley, Donald W. | Pineda-Alvarez, Daniel E. | Kamat, Aparna | Teer, Jamie K. | Cherukuri, Praveen F. | Hansen, Nancy F. | Cruz, Pedro | Young, Alice C. | Berkman, Benjamin E. | ... | Mullikin, James C.
Pediatrics, volume 129, issue 6, pages e1605-e1611 (2012).
10.1542/peds.2011-0080
Cited by (27) | Cite | Source | Open Access
An analysis of exome sequencing for diagnostic testing of the genes associated with muscle disease and spastic paraplegia (journal article)
Dias, Cristina | Sincan, Murat | Cherukuri, Praveen F. | Rupps, Rosemarie | Huang, Yan | Briemberg, Hannah | Selby, Kathryn | Mullikin, James C. | Markello, Thomas C. | Adams, David R. | ... | Boerkoel, Cornelius F.
Human Mutation, volume 33, issue 4, pages 614-626 (2012).
10.1002/humu.22032
Cited by (30) | Cite | Source | Open Access
Exome sequencing and SNP analysis detect novel compound heterozygosity in fatty acid hydroxylase-associated neurodegeneration (journal article)
Pierson, Tyler Mark | Simeonov, Dimitre R | Sincan, Murat | Adams, David A | Markello, Thomas | Golas, Gretchen | Fuentes-Fajardo, Karin | Hansen, Nancy F | Cherukuri, Praveen F | Cruz, Pedro | ... | Gahl, William A
European Journal of Human Genetics, volume 20, issue 4, pages 476-479 (2012).
10.1038/ejhg.2011.222
Cited by (48) | Cite | Source | Open Access
Exon capture analysis of G protein-coupled receptors identifies activating mutations in GRM3 in melanoma (journal article)
Prickett, Todd D | Wei, Xiaomu | Cardenas-Navia, Isabel | Teer, Jamie K | Lin, Jimmy C | Walia, Vijay | Gartner, Jared | Jiang, Jiji | Cherukuri, Praveen F | Molinolo, Alfredo | ... | Samuels, Yardena
Nature Genetics, volume 43, issue 11, pages 1119-1126 (2011).
10.1038/ng.950
Cited by (130) | Cite | Source | Open Access
Genome-wide ChIP-Seq reveals a dramatic shift in the binding of the transcription factor erythroid Kruppel-like factor during erythrocyte differentiation (journal article)
Pilon, Andre M. | Ajay, Subramanian S. | Kumar, Swathi Ashok | Steiner, Laurie A. | Cherukuri, Praveen F. | Wincovitch, Stephen | Anderson, Stacie M. | Mullikin, James C. | Gallagher, Patrick G. | Hardison, Ross C. | ... | Bodine, David M.
Blood, volume 118, issue 17, pages e139-e148 (2011).
10.1182/blood-2011-05-355107
Cited by (87) | Cite | Source | Open Access
Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases (journal article)
Pierson, Tyler Mark | Adams, David | Bonn, Florian | Martinelli, Paola | Cherukuri, Praveen F. | Teer, Jamie K. | Hansen, Nancy F. | Cruz, Pedro | Mullikin for the NISC Comparative Sequencing Program, James C. | Blakesley, Robert W. | ... | Toro, Camilo
PLoS Genetics, volume 7, issue 10, pages e1002325- (2011).
10.1371/journal.pgen.1002325
Cited by (178) | Cite | Source | Open Access
Personalized genomic medicine: Lessons from the exome (journal article)
Solomon, Benjamin D. | Pineda-Alvarez, Daniel E. | Hadley, Donald W. | Teer, Jamie K. | Cherukuri, Praveen F. | Hansen, Nancy F. | Cruz, Pedro | Young, Alice C. | Blakesley, Robert W. | Lanpher, Brendan | ... | Mullikin, James C.
Molecular Genetics and Metabolism, volume 104, issue 1-2, pages 189-191 (2011).
10.1016/j.ymgme.2011.06.022
Cited by (17) | Cite | Source | Open Access