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

Year Number of Results
2012 2
2013 4
2014 4
2015 2
2018 1
2019 6
2020 7
2021 3
2022 9
2023 6
2024 5

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41 results

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Page 1
De novo mutations in moderate or severe intellectual disability.
Hamdan FF, Srour M, Capo-Chichi JM, Daoud H, Nassif C, Patry L, Massicotte C, Ambalavanan A, Spiegelman D, Diallo O, Henrion E, Dionne-Laporte A, Fougerat A, Pshezhetsky AV, Venkateswaran S, Rouleau GA, Michaud JL. Hamdan FF, et al. Among authors: capo chichi jm. PLoS Genet. 2014 Oct 30;10(10):e1004772. doi: 10.1371/journal.pgen.1004772. eCollection 2014 Oct. PLoS Genet. 2014. PMID: 25356899 Free PMC article.
Emerging patterns in clonal haematopoiesis.
Capo-Chichi JM, Michaels P, Tremblay-Le May R, Abelson S, Hasserjian RP, Xia D. Capo-Chichi JM, et al. J Clin Pathol. 2019 Jul;72(7):453-459. doi: 10.1136/jclinpath-2019-205851. Epub 2019 Jun 4. J Clin Pathol. 2019. PMID: 31164443 Review.
Clinical Features and Long-Term Outcomes of a Pan-Canadian Cohort of Adolescents and Young Adults with Myeloproliferative Neoplasms: A Canadian MPN Group Study.
England JT, Szuber N, Sirhan S, Dunne T, Cerquozzi S, Hill M, Villeneuve PJA, Ho JM, Sadikovic B, Bhai P, Krishnan N, Dowhanik S, Hillis C, Capo-Chichi JM, Tsui H, Cheung V, Gauthier K, Sibai H, Davidson MB, Bankar A, Kotchetkov R, Gupta V, Maze D. England JT, et al. Among authors: capo chichi jm. Leukemia. 2024 Mar;38(3):570-578. doi: 10.1038/s41375-024-02155-4. Epub 2024 Feb 6. Leukemia. 2024. PMID: 38321107
Cardiovascular Disease Among Patients With AML and CHIP-Related Mutations.
Calvillo-Argüelles O, Schoffel A, Capo-Chichi JM, Abdel-Qadir H, Schuh A, Carrillo-Estrada M, Liu S, Gupta V, Schimmer AD, Yee K, Shlush LI, Natarajan P, Thavendiranathan P. Calvillo-Argüelles O, et al. Among authors: capo chichi jm. JACC CardioOncol. 2022 Mar 15;4(1):38-49. doi: 10.1016/j.jaccao.2021.11.008. eCollection 2022 Mar. JACC CardioOncol. 2022. PMID: 35492819 Free PMC article.
A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings.
Sam J, Reble E, Kodida R, Shaw A, Clausen M, Salazar MG, Shickh S, Mighton C, Carroll JC, Armel SR, Aronson M, Capo-Chichi JM, Cohn I, Eisen A, Elser C, Graham T, Ott K, Panchal S, Piccinin C, Schrader KA, Kim RH, Lerner-Ellis J, Bombard Y; Incidental Genomics Study Team. Sam J, et al. Among authors: capo chichi jm. Hum Genet. 2022 Dec;141(12):1875-1885. doi: 10.1007/s00439-022-02466-5. Epub 2022 Jun 23. Hum Genet. 2022. PMID: 35739291
41 results