Mark C Hannibal
Associate Professor of Pediatrics
Pediatrics
1500 E Medical Center Dr, D5240 MPB
Ann Arbor, MI 48109-5718
[email protected]

Available to mentor

Mark C Hannibal
Clinical Associate Professor
  • Qualifications
  • Recent Publications
  • Qualifications
    • MD
      University of Michigan Medical School, 1301 Catherine, 1994
    • PhD
      University of Michigan, 1301 Catherine Sr., 1994
    • BA
      Johns Hopkins University, Baltimore, 1986
    Recent Publications See All Publications
    • Journal Article
      Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals.
      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): 100950 DOI:10.1016/j.gim.2023.100950
      PMID: 37551667
    • Journal Article
      Absolute neutrophil count nadir in healthy pediatric patients with the Duffy-null phenotype.
      Merz LE, Li S-H, Ney G, Michniacki TF, Hannibal MC, Walkovich KJ. Blood Adv, 2023 Aug 8; 7 (15): 4182 - 4185. DOI:10.1182/bloodadvances.2023010368
      PMID: 37285802
    • Journal Article
      Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome.
      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. DOI:10.1016/j.jaci.2022.09.002
      PMID: 36228738
    • Preprint
      Aberrant extracellular matrix and cardiac development in models lacking the PR-DUB component ASXL3
      McGrath BT, Tsan YC, Salvi S, Ghali N, Martin DM, Hannibal M, Keegan CE, Helms A, Srivastava A, Bielas SL. 2022 Jul 16; bioRxiv, DOI:10.1101/2022.07.14.500124
    • Journal Article
      eP290: A mosaic Angelman syndrome case with language apraxia and symptoms overlapping Prader-Willi syndrome
      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. DOI:10.1016/j.gim.2022.01.325
    • Proceeding / Abstract / Poster
      Bone Tissue and Osteoblasts from X-linked Type XVIII OI with Defects in Regulated Intramembrane Proteolysis Have Distinct Features
      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.
    • Journal Article
      Novel multilocus imprinting disturbances in a child with expressive language delay and intellectual disability.
      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. DOI:10.1002/ajmg.a.62752
      PMID: 35365979
    • Journal Article
      SOCS1 Haploinsufficiency Presenting as Severe Enthesitis, Bone Marrow Hypocellularity, and Refractory Thrombocytopenia in a Pediatric Patient with Subsequent Response to JAK Inhibition.
      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. DOI:10.1007/s10875-022-01346-x
      PMID: 35976468