Associate Professor of Pediatrics
Pediatrics
1500 E Medical Center Dr, D5240 MPB
Ann Arbor, MI 48109-5718
[email protected]
1500 E Medical Center Dr, D5240 MPB
Ann Arbor, MI 48109-5718
Available to mentor
Mark C Hannibal
Clinical Associate Professor
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MDUniversity of Michigan Medical School, 1301 Catherine, 1994
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PhDUniversity of Michigan, 1301 Catherine Sr., 1994
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BAJohns Hopkins University, Baltimore, 1986
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Bosch E, Popp B, Güse E, Skinner C, van der Sluijs PJ, Maystadt I, Pinto AM, Renieri A, Bruno LP, Granata S, Marcelis C, Baysal Ö, Hartwich D, Holthöfer L, Isidor B, Cogne B, Wieczorek D, Capra V, Scala M, De Marco P, Ognibene M, Jamra RA, Platzer K, Carter LB, Kuismin O, van Haeringen A, Maroofian R, Valenzuela I, Cuscó I, Martinez-Agosto JA, Rabani AM, Mefford HC, Pereira EM, Close C, Anyane-Yeboa K, Wagner M, Hannibal MC, Zacher P, Thiffault I, Beunders G, Umair M, Bhola PT, McGinnis E, Millichap J, van de Kamp JM, Prijoles EJ, Dobson A, Shillington A, Graham BH, Garcia E-J, Galindo MK, Ropers FG, Nibbeling EAR, Hubbard G, Karimov C, Goj G, Bend R, Rath J, Morrow MM, Millan F, Salpietro V, Torella A, Nigro V, Kurki M, Stevenson RE, Santen GWE, Zweier M, Campeau PM, Severino M, Reis A, Accogli A, Vasileiou G. Genet Med, 2023 Nov; 25 (11): 100950Journal ArticleElucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals.
DOI:10.1016/j.gim.2023.100950 PMID: 37551667 -
Merz LE, Li S-H, Ney G, Michniacki TF, Hannibal MC, Walkovich KJ. Blood Adv, 2023 Aug 8; 7 (15): 4182 - 4185.Journal ArticleAbsolute neutrophil count nadir in healthy pediatric patients with the Duffy-null phenotype.
DOI:10.1182/bloodadvances.2023010368 PMID: 37285802 -
Leiding JW, Vogel TP, Santarlas VGJ, Mhaskar R, Smith MR, Carisey A, Vargas-Hernández A, Silva-Carmona M, Heeg M, Rensing-Ehl A, Neven B, Hadjadj J, Hambleton S, Ronan Leahy T, Meesilpavikai K, Cunningham-Rundles C, Dutmer CM, Sharapova SO, Taskinen M, Chua I, Hague R, Klemann C, Kostyuchenko L, Morio T, Thatayatikom A, Ozen A, Scherbina A, Bauer CS, Flanagan SE, Gambineri E, Giovannini-Chami L, Heimall J, Sullivan KE, Allenspach E, Romberg N, Deane SG, Prince BT, Rose MJ, Bohnsack J, Mousallem T, Jesudas R, Santos Vilela MMD, O'Sullivan M, Pachlopnik Schmid J, Průhová Š, Klocperk A, Rees M, Su H, Bahna S, Baris S, Bartnikas LM, Chang Berger A, Briggs TA, Brothers S, Bundy V, Chan AY, Chandrakasan S, Christiansen M, Cole T, Cook MC, Desai MM, Fischer U, Fulcher DA, Gallo S, Gauthier A, Gennery AR, Gonçalo Marques J, Gottrand F, Grimbacher B, Grunebaum E, Haapaniemi E, Hämäläinen S, Heiskanen K, Heiskanen-Kosma T, Hoffman HM, Gonzalez-Granado LI, Guerrerio AL, Kainulainen L, Kumar A, Lawrence MG, Levin C, Martelius T, Neth O, Olbrich P, Palma A, Patel NC, Pozos T, Preece K, Lugo Reyes SO, Russell MA, Schejter Y, Seroogy C, Sinclair J, Skevofilax E, Suan D, Suez D, Szabolcs P, Velasco H, Warnatz K, Walkovich K, Worth A, STAT3 GOF Working Group members , Seppänen MRJ, Torgerson TR, Sogkas G, Ehl S, Tangye SG, Cooper MA, Milner JD, Forbes Satter LR. J Allergy Clin Immunol, 2023 Apr; 151 (4): 1081 - 1095.Journal ArticleMonogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome.
DOI:10.1016/j.jaci.2022.09.002 PMID: 36228738 -
McGrath BT, Tsan YC, Salvi S, Ghali N, Martin DM, Hannibal M, Keegan CE, Helms A, Srivastava A, Bielas SL. 2022 Jul 16; bioRxiv,PreprintAberrant extracellular matrix and cardiac development in models lacking the PR-DUB component ASXL3
DOI:10.1101/2022.07.14.500124 -
Yang C, Sloan-Heggen C, Ducharme N, Bienemann L, Sarchenko J, Kubisak A, LeSueur K, Hannibal M, Innis J. Genetics in Medicine, 2022 Mar; 24 (3): s183 - s184.Journal ArticleeP290: A mosaic Angelman syndrome case with language apraxia and symptoms overlapping Prader-Willi syndrome
DOI:10.1016/j.gim.2022.01.325 -
Zarei A, Fratzl-Zelman N, An DD, Glassford M, Hannibal M, Wallace M, Esposito PW, Franzone JM, Lindstrom K, Zwerina J, Knue M, Talvacchio S, Marini JC. JOURNAL OF BONE AND MINERAL RESEARCH, 2022 37: 169 - 170.Proceeding / Abstract / PosterBone Tissue and Osteoblasts from X-linked Type XVIII OI with Defects in Regulated Intramembrane Proteolysis Have Distinct Features
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Tayeh MK, DeVaul J, LeSueur K, Yang C, Bedoyan JK, Thomas P, Hannibal MC, Innis JW. Am J Med Genet A, 2022 Jul; 188 (7): 2209 - 2216.Journal ArticleNovel multilocus imprinting disturbances in a child with expressive language delay and intellectual disability.
DOI:10.1002/ajmg.a.62752 PMID: 35365979 -
Michniacki TF, Walkovich K, DeMeyer L, Saad N, Hannibal M, Basiaga ML, Horst KK, Mohan S, Chen L, Brodeur K, Du Y, Frame D, Ngo S, Simoneau J, Brown N, Lee PY. J Clin Immunol, 2022 Nov; 42 (8): 1766 - 1777.Journal ArticleSOCS1 Haploinsufficiency Presenting as Severe Enthesitis, Bone Marrow Hypocellularity, and Refractory Thrombocytopenia in a Pediatric Patient with Subsequent Response to JAK Inhibition.
DOI:10.1007/s10875-022-01346-x PMID: 35976468