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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2019 2
2020 3
2021 2
2022 3
2023 5
2024 0

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14 results

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Page 1
Germline genetic variants and pediatric rhabdomyosarcoma outcomes: a report from the Children's Oncology Group.
Martin-Giacalone BA, Richard MA, Scheurer ME, Khan J, Sok P, Shetty PB, Chanock SJ, Li SA, Yeager M, Marquez-Do DA, Barkauskas DA, Hall D, McEvoy MT, Brown AL, Sabo A, Scheet P, Huff CD, Skapek SX, Hawkins DS, Venkatramani R, Mirabello L, Lupo PJ. Martin-Giacalone BA, et al. Among authors: sok p. J Natl Cancer Inst. 2023 Jun 8;115(6):733-741. doi: 10.1093/jnci/djad055. J Natl Cancer Inst. 2023. PMID: 36951526 Free PMC article.
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants.
Sok P, Sabo A, Almli LM, Jenkins MM, Nembhard WN, Agopian AJ, Bamshad MJ, Blue EE, Brody LC, Brown AL, Browne ML, Canfield MA, Carmichael SL, Chong JX, Dugan-Perez S, Feldkamp ML, Finnell RH, Gibbs RA, Kay DM, Lei Y, Meng Q, Moore CA, Mullikin JC, Muzny D, Olshan AF, Pangilinan F, Reefhuis J, Romitti PA, Schraw JM, Shaw GM, Werler MM, Harpavat S, Lupo PJ; University of Washington Center for Mendelian Genomics, NISC Comparative Sequencing Program, the National Birth Defects Prevention Study. Sok P, et al. Am J Med Genet A. 2023 Jun;191(6):1546-1556. doi: 10.1002/ajmg.a.63185. Epub 2023 Mar 21. Am J Med Genet A. 2023. PMID: 36942736
Epigenome-wide association study of acute lymphoblastic leukemia in children with Down syndrome.
Li S, Sok P, Xu K, Muskens IS, Elliott N, Myint SS, Pandey P, Hansen HM, Morimoto LM, Kang AY, Metayer C, Ma X, Mueller BA, Roy A, Roberts I, Rabin KR, Brown AL, Lupo PJ, Wiemels JL, de Smith AJ. Li S, et al. Among authors: sok p. Blood Adv. 2022 Jul 26;6(14):4132-4136. doi: 10.1182/bloodadvances.2022007098. Blood Adv. 2022. PMID: 35588500 Free PMC article. No abstract available.
The role of genetic variation in DGKK on moderate and severe hypospadias.
Richard MA, Sok P, Canon S, Brown AL, Peckham-Gregory EC, Nembhard WN, Carmichael SL, Ehli EA, Kallsen NA, Peyton SA, Davies GE, Patel A, Zamilpa I, Wyatt RA, Hobbs CA, Scheurer ME, Lupo PJ. Richard MA, et al. Among authors: sok p. Birth Defects Res. 2019 Aug 1;111(13):932-937. doi: 10.1002/bdr2.1522. Epub 2019 May 18. Birth Defects Res. 2019. PMID: 31102501 Free PMC article.
14 results