| Year |
Citation |
Score |
| 2017 |
Krishnan S, Perlina A, Thomas A, Kakaradov B, Delport W, Nehring RB, Shinbrot E, Natarajan TG, Lau CK, Gylfe AE, Sainger R, Pelak K, Smith HL, Biggs W, Perkins B, et al. Comprehensive analysis of tumor NGS data to demonstrate pathways pointing to therapeutic targeting options. Journal of Clinical Oncology. 35: e23153-e23153. DOI: 10.1200/Jco.2017.35.15_Suppl.E23153 |
0.419 |
|
| 2017 |
Gylfe AE, Shinbrot E, Kakaradov B, Delport W, Lau CK, Krishnan S, Perlina A, Natarajan TG, Sainger R, Pelak K, Choppa P, Cooc J, Biggs W, Smith HL, Perkins B, et al. Tumor profiling from whole-genome and whole transcriptome sequencing to uncover gene fusions and structural variations in clinically relevant cancer genes. Journal of Clinical Oncology. 35: e23118-e23118. DOI: 10.1200/Jco.2017.35.15_Suppl.E23118 |
0.492 |
|
| 2016 |
He J, Abdel-Wahab O, Nahas MK, Wang K, Rampal RK, Intlekofer AM, Patel J, Krivstov A, Frampton GM, Young LE, Zhong S, Bailey M, White JR, Roels S, Deffenbaugh J, ... ... Pelak K, et al. Integrated genomic DNA/RNA profiling of hematologic malignancies in the clinical setting. Blood. PMID 26966091 DOI: 10.1182/Blood-2015-08-664649 |
0.519 |
|
| 2014 |
Nelson CL, Pelak K, Podgoreanu MV, Ahn SH, Scott WK, Allen AS, Cowell LG, Rude TH, Zhang Y, Tong A, Ruffin F, Sharma-Kuinkel BK, Fowler VG. A genome-wide association study of variants associated with acquisition of Staphylococcus aureus bacteremia in a healthcare setting. Bmc Infectious Diseases. 14: 83. PMID 24524581 DOI: 10.1186/1471-2334-14-83 |
0.486 |
|
| 2013 |
Ruzzo EK, Capo-Chichi JM, Ben-Zeev B, Chitayat D, Mao H, Pappas AL, Hitomi Y, Lu YF, Yao X, Hamdan FF, Pelak K, Reznik-Wolf H, Bar-Joseph I, Oz-Levi D, Lev D, et al. Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathy. Neuron. 80: 429-41. PMID 24139043 DOI: 10.1016/J.Neuron.2013.08.013 |
0.361 |
|
| 2013 |
Lane J, McLaren PJ, Dorrell L, Shianna KV, Stemke A, Pelak K, Moore S, Oldenburg J, Alvarez-Roman MT, Angelillo-Scherrer A, Boehlen F, Bolton-Maggs PH, Brand B, Brown D, Chiang E, et al. A genome-wide association study of resistance to HIV infection in highly exposed uninfected individuals with hemophilia A. Human Molecular Genetics. 22: 1903-10. PMID 23372042 DOI: 10.1093/Hmg/Ddt033 |
0.541 |
|
| 2013 |
Pelak K, Wright J, Yan Z, Darwanto A, Liu W, Fang P, Li J, Sankar S, Galderisi C. Abstract 3509: Complementary analysis of LKB1/STK11 mutation and protein expression status using next-generation sequencing, Sanger sequencing and immunohistochemistry. Cancer Research. 73: 3509-3509. DOI: 10.1158/1538-7445.Am2013-3509 |
0.457 |
|
| 2013 |
Fang P, Darwanto A, Yan Z, Liu W, Pelak K, Kristof J, Mack PC, Sankar S, Galderisi C, Li J. Abstract A208: Mutation detection in FFPE and plasma circulating DNA with a focused ALK-EGFR-KRAS Next-Generation Sequencing panel. Molecular Cancer Therapeutics. 12. DOI: 10.1158/1535-7163.Targ-13-A208 |
0.316 |
|
| 2012 |
Oz-Levi D, Ben-Zeev B, Ruzzo EK, Hitomi Y, Gelman A, Pelak K, Anikster Y, Reznik-Wolf H, Bar-Joseph I, Olender T, Alkelai A, Weiss M, Ben-Asher E, Ge D, Shianna KV, et al. Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesis. American Journal of Human Genetics. 91: 1065-72. PMID 23176824 DOI: 10.1016/J.Ajhg.2012.09.015 |
0.414 |
|
| 2012 |
Zhu M, Need AC, Han Y, Ge D, Maia JM, Zhu Q, Heinzen EL, Cirulli ET, Pelak K, He M, Ruzzo EK, Gumbs C, Singh A, Feng S, Shianna KV, et al. Using ERDS to infer copy-number variants in high-coverage genomes. American Journal of Human Genetics. 91: 408-21. PMID 22939633 DOI: 10.1016/J.Ajhg.2012.07.004 |
0.646 |
|
| 2012 |
McLaren PJ, Ripke S, Pelak K, Weintrob AC, Patsopoulos NA, Jia X, Erlich RL, Lennon NJ, Kadie CM, Heckerman D, Gupta N, Haas DW, Deeks SG, Pereyra F, Walker BD, et al. Fine-mapping classical HLA variation associated with durable host control of HIV-1 infection in African Americans. Human Molecular Genetics. 21: 4334-47. PMID 22718199 DOI: 10.1093/Hmg/Dds226 |
0.34 |
|
| 2011 |
Pelak K, Need AC, Fellay J, Shianna KV, Feng S, Urban TJ, Ge D, De Luca A, Martinez-Picado J, Wolinsky SM, Martinson JJ, Jamieson BD, Bream JH, Martin MP, Borrow P, et al. Copy number variation of KIR genes influences HIV-1 control. Plos Biology. 9: e1001208. PMID 22140359 DOI: 10.1371/Journal.Pbio.1001208 |
0.465 |
|
| 2011 |
Ge D, Ruzzo EK, Shianna KV, He M, Pelak K, Heinzen EL, Need AC, Cirulli ET, Maia JM, Dickson SP, Zhu M, Singh A, Allen AS, Goldstein DB. SVA: software for annotating and visualizing sequenced human genomes. Bioinformatics (Oxford, England). 27: 1998-2000. PMID 21624899 DOI: 10.1093/Bioinformatics/Btr317 |
0.646 |
|
| 2010 |
Pelak K, Shianna KV, Ge D, Maia JM, Zhu M, Smith JP, Cirulli ET, Fellay J, Dickson SP, Gumbs CE, Heinzen EL, Need AC, Ruzzo EK, Singh A, Campbell CR, et al. The characterization of twenty sequenced human genomes. Plos Genetics. 6: e1001111. PMID 20838461 DOI: 10.1371/Journal.Pgen.1001111 |
0.667 |
|
| 2010 |
Pelak K, Goldstein DB, Walley NM, Fellay J, Ge D, Shianna KV, Gumbs C, Gao X, Maia JM, Cronin KD, Hussain SK, Carrington M, Michael NL, Weintrob AC, et al. Host determinants of HIV-1 control in African Americans. The Journal of Infectious Diseases. 201: 1141-9. PMID 20205591 DOI: 10.1086/651382 |
0.505 |
|
| 2009 |
Urban TJ, Weintrob AC, Fellay J, Colombo S, Shianna KV, Gumbs C, Rotger M, Pelak K, Dang KK, Detels R, Martinson JJ, O'Brien SJ, Letvin NL, McMichael AJ, Haynes BF, et al. CCL3L1 and HIV/AIDS susceptibility. Nature Medicine. 15: 1110-2. PMID 19812560 DOI: 10.1038/Nm1009-1110 |
0.376 |
|
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