Co-Authors
This is a "connection" page, showing publications co-authored by PAUL A SCHEET and CHAD HUFF.
Connection Strength
1.006
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A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic cancer risk. HGG Adv. 2022 Jan 13; 3(1):100078.
Score: 0.212
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Integrated case-control and somatic-germline interaction analyses of soft-tissue sarcoma. J Med Genet. 2021 03; 58(3):145-153.
Score: 0.191
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XPAT: a toolkit to conduct cross-platform association studies with heterogeneous sequencing datasets. Nucleic Acids Res. 2018 04 06; 46(6):e32.
Score: 0.165
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Integrated case-control and somatic-germline interaction analyses of melanoma susceptibility genes. Biochim Biophys Acta Mol Basis Dis. 2018 Jun; 1864(6 Pt B):2247-2254.
Score: 0.162
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A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data. Nat Biotechnol. 2014 Jul; 32(7):663-9.
Score: 0.126
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Germline genetic variants and pediatric rhabdomyosarcoma outcomes: a report from the Children's Oncology Group. J Natl Cancer Inst. 2023 06 08; 115(6):733-741.
Score: 0.059
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Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium Study. Eur Urol Oncol. 2021 08; 4(4):570-579.
Score: 0.050
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DNA Sequencing of Small Bowel Adenocarcinomas Identifies Targetable Recurrent Mutations in the ERBB2 Signaling Pathway. Clin Cancer Res. 2019 01 15; 25(2):641-651.
Score: 0.043