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The Spectrum of SPTA1-Associated Hereditary Spherocytosis.
Chonat S, Risinger M, Sakthivel H, Niss O, Rothman JA, Hsieh L, Chou ST, Kwiatkowski JL, Khandros E, Gorman MF, Wells DT, Maghathe T, Dagaonkar N, Seu KG, Zhang K, Zhang W, Kalfa TA. Chonat S, et al. Among authors: zhang w, zhang k. Front Physiol. 2019 Jul 3;10:815. doi: 10.3389/fphys.2019.00815. eCollection 2019. Front Physiol. 2019. PMID: 31333484 Free PMC article.
Corrigendum: The Spectrum of SPTA1-Associated Hereditary Spherocytosis.
Chonat S, Risinger M, Sakthivel H, Niss O, Rothman JA, Hsieh L, Chou ST, Kwiatkowski JL, Khandros E, Gorman MF, Wells DT, Maghathe T, Dagaonkar N, Seu KG, Zhang K, Zhang W, Kalfa TA. Chonat S, et al. Among authors: zhang w, zhang k. Front Physiol. 2019 Oct 18;10:1331. doi: 10.3389/fphys.2019.01331. eCollection 2019. Front Physiol. 2019. PMID: 31736770 Free PMC article.
VPS4A Mutations in Humans Cause Syndromic Congenital Dyserythropoietic Anemia due to Cytokinesis and Trafficking Defects.
Seu KG, Trump LR, Emberesh S, Lorsbach RB, Johnson C, Meznarich J, Underhill HR, Chou ST, Sakthivel H, Nassar NN, Seu KJ, Blanc L, Zhang W, Lutzko CM, Kalfa TA. Seu KG, et al. Among authors: zhang w. Am J Hum Genet. 2020 Dec 3;107(6):1149-1156. doi: 10.1016/j.ajhg.2020.10.013. Epub 2020 Nov 12. Am J Hum Genet. 2020. PMID: 33186543 Free PMC article.
Congenital dyserythropoietic anemia type I: First report from the Congenital Dyserythropoietic Anemia Registry of North America (CDAR).
Niss O, Lorsbach RB, Berger M, Chonat S, McLemore M, Buchbinder D, McCavit T, Shaffer LG, Simpson J, Schwartz JH, Meznarich J, Emberesh M, Seu KG, Zhang W, Kalfa TA; CDAR consortium. Niss O, et al. Among authors: zhang w. Blood Cells Mol Dis. 2021 Mar;87:102534. doi: 10.1016/j.bcmd.2020.102534. Epub 2020 Dec 24. Blood Cells Mol Dis. 2021. PMID: 33401150 Free PMC article. Clinical Trial.
Hemolytic anemia and macrothrombocytopenia: A lipid problem?
Risinger M, Kim PS, Rodriguez RX, Narvaez Rivas M, Setchell KDR, Zhang W, Kalfa TA. Risinger M, et al. Among authors: zhang w. Am J Hematol. 2023 Aug;98(8):1335-1340. doi: 10.1002/ajh.26916. Epub 2023 Apr 8. Am J Hematol. 2023. PMID: 36974979 No abstract available.
Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group.
Schmidt RJ, Steeves M, Bayrak-Toydemir P, Benson KA, Coe BP, Conlin LK, Ganapathi M, Garcia J, Gollob MH, Jobanputra V, Luo M, Ma D, Maston G, McGoldrick K, Palculict TB, Pesaran T, Pollin TI, Qian E, Rehm HL, Riggs ER, Schilit SLP, Sergouniotis PI, Tvrdik T, Watkins N, Zec L, Zhang W, Lebo MS; ClinGen Low Penetrance/Risk Allele Working Group. Schmidt RJ, et al. Among authors: zhang w. Genet Med. 2024 Mar;26(3):101036. doi: 10.1016/j.gim.2023.101036. Epub 2023 Dec 3. Genet Med. 2024. PMID: 38054408
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