Medical College of Wisconsin
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Mariko Suchi MD, PhD

Mariko Suchi MD, PhD profile photo picture

Associate Professor

Institution: Medical College of Wisconsin
Department: Pathology
Division: Administration
Program: Pediatrics

View Curriculum Vitae

Publications (58)

  • Diffuse Esophageal Papillomatosis. (Bashir A, Suchi M, Martinez AM) J Pediatr Gastroenterol Nutr 2022 Aug 03 PMID: 35929991 08/06/2022    
  • ALK-positiveA histiocytosis: a new clinicopathologic spectrum highlighting neurologic involvement and responses to ALK inhibition. (Kemps PG, Picarsic J, Durham BH, H??lias-Rodzewicz Z, Hiemcke-Jiwa L, van den Bos C, van de Wetering MD, van Noesel CJM, van Laar JAM, Verdijk RM, Flucke UE, Hogendoorn PCW, Woei-A-Jin FJSH, Sciot R, Beilken A, Feuerhake F, Ebinger M, M??hle R, Fend F, Bornemann A, Wiegering V, Ernestus K, M??ry T, Gryniewicz-Kwiatkowska O, Dembowska-Baginska B, Evseev DA, Potapenko V, Baykov VV, Gaspari S, Rossi S, Gessi M, Tamburrini G, H??ritier S, Donadieu J, Bonneau-Lagacherie J, Lamaison C, Farnault L, Fraitag S, Julli?? ML, Haroche J, Collin M, Allotey J, Madni M, Turner K, Picton S, Barbaro PM, Poulin A, Tam IS, El Demellawy D, Empringham B, Whitlock JA, Raghunathan A, Swanson AA, Suchi M, Brandt JM, Yaseen NR, Weinstein JL, Eldem I, Sisk BA, Sridhar V, Atkinson M, Massoth LR, Hornick JL, Alexandrescu S, Yeo KK, Petrova-Drus K, Peeke SZ, Mu??oz-Arcos LS, Leino DG, Grier DD, Lorsbach R, Roy S, Kumar AR, Garg S, Tiwari N, Schafernak KT, Henry MM, van Halteren AGS, Abla O, Diamond EL, Emile JF) Blood 2022 01 13;139(2):256-280 PMID: 34727172 PMCID: PMC8759533 SCOPUS ID: 2-s2.0-85122787125 11/03/2021       7 Citations
  • Esophageal Granular Cell Tumor. (Bashir A, Suchi M, Martinez AM, Lerner D) J Pediatr Gastroenterol Nutr 2021 12 01;73(6):e126 PMID: 34347679 SCOPUS ID: 2-s2.0-85122111088 08/05/2021       1 Citation
  • Bone Marrow Suppression Associated With Celiac Disease in a 4-Year-Old Boy. (Watson A, Kolinski J, Suchi M, Elkadri A) ACG Case Rep J 2021 Feb;8(2):e00538 PMID: 33644248 PMCID: PMC7904273 03/02/2021    
  • Liver failure and x-linked immunodeficiency type 47. (Gumm AJ, Basel DG, Thakrar P, Suchi M, Telega G) Pediatr Transplant 2020 12;24(8):e13808 PMID: 32790950 SCOPUS ID: 2-s2.0-85089391265 08/14/2020       1 Citation
  • Multimodal Therapy Including Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy Can Result in Long-term Disease-free Survival in Pediatric Desmoplastic Small Round Cell Tumor With Extraperitoneal Disease. (Xiao J, Browning MB, Boyd KP, Suchi M, Turaga KK, Firat SY, Mortland LJ, Lal DR) J Pediatr Hematol Oncol 2021 08 01;43(6):228-231 PMID: 32555030 SCOPUS ID: 2-s2.0-85086724925 06/20/2020    
  • Submucosal Supernumerary Smooth Muscle Coat: A Common Histologic Finding in Mowat-Wilson Syndrome With or Without Hirschsprung Disease. (Suchi M, Calkins CM, Chogle A, Bond JS, Kapur RP) Pediatr Dev Pathol 2020 Sep-Oct;23(5):372-379 PMID: 32469269 SCOPUS ID: 2-s2.0-85085628515 05/30/2020    
  • Large expansile lesion of left posterior mandible. (Gill D, Padilla R, Giorgadze T, Suchi M, Brookes C) Oral Surg Oral Med Oral Pathol Oral Radiol 2020 Mar;129(3):177-183 PMID: 31932252 SCOPUS ID: 2-s2.0-85077718793 01/15/2020    
  • Diffuse Midline Glioma With Osseous Metastases at Diagnosis: A Case Report. (Bhatt NS, Houser K, Belongia M, Ellison DW, Foy A, Jarzembowski J, Kelly T, Maheshwari M, Suchi M, Knipstein J) J Pediatr Hematol Oncol 2020 10;42(7):e673-e676 PMID: 31568066 SCOPUS ID: 2-s2.0-85091808908 10/01/2019       4 Citations
  • Ganglioglioma in a Survivor of Infantile Glioblastoma. (Scheuermann A, Belongia M, Lawlor MW, Suchi M, Kaufman B, Vasudevaraja V, Serrano J, Snuderl M, Knipstein J) J Pediatr Hematol Oncol 2020 01;42(1):e56-e60 PMID: 30676438 SCOPUS ID: 2-s2.0-85060368706 01/25/2019       2 Citations
  • Spheno-Orbital Aneurysmal Bone Cyst in a 10-Month-Old Infant. (Arocho-Quinones EV, Self S, Suchi M, Zwagerman NT, Lew SM) World Neurosurg 2018 Sep;117:371-376 PMID: 30157596 SCOPUS ID: 2-s2.0-85050132264 08/31/2018       1 Citation
  • A Rare Case Of a 2-year-old Boy With Alagille Syndrome and Type 3 Hereditary Hemochromatosis With TFR2 Mutation. (Khayat AA, Suchi M, Vitola B) J Pediatr Gastroenterol Nutr 2019 Apr;68(4):e68-e70 PMID: 29985876 SCOPUS ID: 2-s2.0-85063633970 07/10/2018       1 Citation
  • A model of TH17-associated ileal hyperplasia that requires both IL-17A and IFNI? to generate self-tolerance and prevent colitis. (Jeschke JC, Mayne CG, Ziegelbauer J, DeCiantis CL, Singh S, Kumar SN, Suchi M, Iwakura Y, Drobyski WR, Salzman NH, Williams CB) Mucosal Immunol 2018 07;11(4):1127-1137 PMID: 29728642 PMCID: PMC6571016 SCOPUS ID: 2-s2.0-85046438531 05/08/2018       2 Citations
  • Expanding the Phenotype of ALK-positive Histiocytosis: A Report of 2 Cases. (Huang H, Gheorghe G, North PE, Suchi M) Pediatr Dev Pathol 2018 Sep-Oct;21(5):449-455 PMID: 29224419 SCOPUS ID: 2-s2.0-85053878415 12/12/2017       20 Citations
  • Successful Treatment of Invasive Conidiobolus Infection During Therapy for Acute Lymphoblastic Leukemia. (Erker C, Huppler AR, Walsh TJ, McCormick ME, Suchi M, Bhatt NS, Kehl SC, Southwood J, Harker-Murray P) J Pediatr Hematol Oncol 2018 10;40(7):e446-e449 PMID: 28991126 PMCID: PMC5904005 SCOPUS ID: 2-s2.0-85031495362 10/11/2017       6 Citations
  • Herpes Simplex Virus Esophagitis in Immunocompetent Children: A Harbinger of Eosinophilic Esophagitis? (Fritz J, Lerner D, Suchi M) J Pediatr Gastroenterol Nutr 2018 04;66(4):609-613 PMID: 28937540 SCOPUS ID: 2-s2.0-85044226710 09/25/2017       23 Citations
  • Langerhans cell histiocytosis of the digestive tract identified on an upper gastrointestinal examination. (Zei M, Meyers AB, Boyd KP, Larson-Nath C, Suchi M) Pediatr Radiol 2016 Aug;46(9):1341-4 PMID: 26886914 SCOPUS ID: 2-s2.0-84958817648 02/18/2016       3 Citations
  • A Case of Necrotizing Epiglottitis Due to Nontoxigenic Corynebacterium diphtheriae. (Lake JA, Ehrhardt MJ, Suchi M, Chun RH, Willoughby RE) Pediatrics 2015 Jul;136(1):e242-5 PMID: 26055849 SCOPUS ID: 2-s2.0-84934289025 06/10/2015       9 Citations
  • Lingual hamartoma associated with a cleft palate in a newborn. (Daramola OO, Suchi M, Chun RH) Ear Nose Throat J 2014 Oct-Nov;93(10-11):E9-11 PMID: 25397398 SCOPUS ID: 2-s2.0-84949195415 11/15/2014       2 Citations
  • Bronchogenic cyst in the intradiaphragmatic location. (Subramanian S, Chandra T, Whitehouse J, Suchi M, Arca M, Maheshwari M) WMJ 2013 Dec;112(6):262-4 PMID: 24511867 SCOPUS ID: 2-s2.0-84890546003 02/12/2014       9 Citations
  • Pancreatic histopathology of hyperinsulinism (Suchi M, Bhatti TR, Ruchelli E) Frontiers in Diabetes 2012;21:57-70 SCOPUS ID: 2-s2.0-84859166213 04/04/2012    
  • The pancreas (Suchi M) Stocker and Dehner's Pediatric Pathology: Third Edition 28 March 2012 SCOPUS ID: 2-s2.0-84973517690 03/28/2012    
  • Pancreatic histopathology of hyperinsulinism (Suchi M, Bhattic TR, Ruchellic ED) Monogenic Hyperinsulinemic Hypoglycemia Disorders February 16, 2012;21:57-70 SCOPUS ID: 2-s2.0-84909995837 02/16/2012       3 Citations
  • Cecal granular cell tumor. (Sultan MI, Suchi M, Werlin SL) J Pediatr Gastroenterol Nutr 2011 Apr;52(4):375 PMID: 21407113 SCOPUS ID: 2-s2.0-79953822080 03/17/2011       4 Citations
  • Fetal lung interstitial tumor (FLIT): A proposed newly recognized lung tumor of infancy to be differentiated from cystic pleuropulmonary blastoma and other developmental pulmonary lesions. (Dishop MK, McKay EM, Kreiger PA, Priest JR, Williams GM, Langston C, Jarzembowski J, Suchi M, Dehner LP, Hill DA) Am J Surg Pathol 2010 Dec;34(12):1762-72 PMID: 21107081 SCOPUS ID: 2-s2.0-78650396655 11/26/2010       44 Citations
  • Multifocal vulvar smooth muscle tumor with an unusual intravascular growth pattern and multiple local recurrences in a 10-year-old child: a diagnostic dilemma. (Harrington A, Bell E, Suchi M, Behmaram B, Uyar D) Pediatr Dev Pathol 2011 May-Jun;14(3):235-9 PMID: 21090988 SCOPUS ID: 2-s2.0-80054051952 11/26/2010       1 Citation
  • An autoinflammatory disease due to homozygous deletion of the IL1RN locus. (Reddy S, Jia S, Geoffrey R, Lorier R, Suchi M, Broeckel U, Hessner MJ, Verbsky J) N Engl J Med 2009 Jun 04;360(23):2438-44 PMID: 19494219 PMCID: PMC2803085 SCOPUS ID: 2-s2.0-66649113371 06/06/2009       307 Citations
  • Extremes of clinical and enzymatic phenotypes in children with hyperinsulinism caused by glucokinase activating mutations. (Sayed S, Langdon DR, Odili S, Chen P, Buettger C, Schiffman AB, Suchi M, Taub R, Grimsby J, Matschinsky FM, Stanley CA) Diabetes 2009 Jun;58(6):1419-27 PMID: 19336674 PMCID: PMC2682682 SCOPUS ID: 2-s2.0-66649108506 04/02/2009       80 Citations
  • Diagnosis and localization of focal congenital hyperinsulinism by 18F-fluorodopa PET scan. (Hardy OT, Hernandez-Pampaloni M, Saffer JR, Suchi M, Ruchelli E, Zhuang H, Ganguly A, Freifelder R, Adzick NS, Alavi A, Stanley CA) J Pediatr 2007 Feb;150(2):140-5 PMID: 17236890 SCOPUS ID: 2-s2.0-33846198883 01/24/2007       124 Citations
  • Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism. (Suchi M, MacMullen CM, Thornton PS, Adzick NS, Ganguly A, Ruchelli ED, Stanley CA) Mod Pathol 2006 Jan;19(1):122-9 PMID: 16357843 SCOPUS ID: 2-s2.0-32844459139 12/17/2005       60 Citations
  • Erratum: Molecular characterization of histidinemia: Identification of four missense mutations in the histidase gene (Human Genetics (2005) vol. 116 (340-346) 10.1007/s00439-004-1232-5) (Kawai Y, Moriyama A, Asai K, Coleman-Campbell CM, Sumi S, Morishita H, Suchi M) Human Genetics December 2005;118(3-4):531-532 SCOPUS ID: 2-s2.0-30744438330 12/01/2005    
  • Chromophobe renal cell carcinoma in a pediatric living-related kidney transplant recipient. (Greco AJ, Baluarte JH, Meyers KE, Sellers MT, Suchi M, Biegel JA, Kaplan BS) Am J Kidney Dis 2005 Jun;45(6):e105-8 PMID: 15957121 SCOPUS ID: 2-s2.0-20444397065 06/16/2005       19 Citations
  • Molecular characterization of histidinemia: identification of four missense mutations in the histidase gene. (Kawai Y, Moriyama A, Asai K, Coleman-Campbell CM, Sumi S, Morishita H, Suchi M) Hum Genet 2005 Apr;116(5):340-6 PMID: 15806399 SCOPUS ID: 2-s2.0-17144419687 04/05/2005       19 Citations
  • Erratum: Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation (The Journal of Clinical Endocrinology and Metabolism (2004) 89 (288-296)) (Stanley CA, Thornton PS, Ganguly A, MacMullen C, Underwood P, Bhatia P, Steinkrauss L, Wanner L, Kaye R, Ruchelli E, Suchi M, Adzick NS) Journal of Clinical Endocrinology and Metabolism January 2005;90(1):189 SCOPUS ID: 2-s2.0-19944427004 01/01/2005       2 Citations
  • Congenital hyperinsulinism: intraoperative biopsy interpretation can direct the extent of pancreatectomy. (Suchi M, Thornton PS, Adzick NS, MacMullen C, Ganguly A, Stanley CA, Ruchelli ED) Am J Surg Pathol 2004 Oct;28(10):1326-35 PMID: 15371948 SCOPUS ID: 2-s2.0-5044232961 09/17/2004       55 Citations
  • Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation. (Stanley CA, Thornton PS, Ganguly A, MacMullen C, Underwood P, Bhatia P, Steinkrauss L, Wanner L, Kaye R, Ruchelli E, Suchi M, Adzick NS) J Clin Endocrinol Metab 2004 Jan;89(1):288-96 PMID: 14715863 SCOPUS ID: 2-s2.0-10744221944 01/13/2004       101 Citations
  • Histopathology of congenital hyperinsulinism: retrospective study with genotype correlations. (Suchi M, MacMullen C, Thornton PS, Ganguly A, Stanley CA, Ruchelli ED) Pediatr Dev Pathol 2003 Jul-Aug;6(4):322-33 PMID: 14692646 SCOPUS ID: 2-s2.0-0141650394 12/25/2003       63 Citations
  • Noncardiogenic pulmonary edema as the chief manifestation of a pheochromocytoma: a case report of MEN 2A with pedigree analysis of the RET proto-oncogene. (Okada Y, Suchi M, Takeyama H, Hodgson ME, Kato T, Manabe T) Tohoku J Exp Med 1999 Jun;188(2):177-87 PMID: 10526879 SCOPUS ID: 2-s2.0-0033143130 10/20/1999       8 Citations
  • Hereditary orotic aciduria heterozygotes accompanied with neurological symptoms. (Imaeda M, Sumi S, Imaeda H, Suchi M, Kidouchi K, Togari H, Wada Y) Tohoku J Exp Med 1998 May;185(1):67-70 PMID: 9710947 SCOPUS ID: 2-s2.0-0032064818 08/26/1998       7 Citations
  • [Hereditary orotic aciduria]. (Mizuno H, Suchi M, Wada Y) Ryoikibetsu Shokogun Shirizu 1998(18 Pt 1):484-6 PMID: 9590108 SCOPUS ID: 2-s2.0-0031629731 05/20/1998    
  • Isolation of a rat histidase cDNA sequence and expression in Escherichia coli--evidence of extrahepatic/epidermal distribution. (Sano H, Tada T, Moriyama A, Ogawa H, Asai K, Kawai Y, Hodgson ME, Kato T, Wada Y, Suchi M) Eur J Biochem 1997 Nov 15;250(1):212-21 PMID: 9432011 SCOPUS ID: 2-s2.0-9844256437 02/07/1998       11 Citations
  • Molecular cloning of the human UMP synthase gene and characterization of point mutations in two hereditary orotic aciduria families. (Suchi M, Mizuno H, Kawai Y, Tsuboi T, Sumi S, Okajima K, Hodgson ME, Ogawa H, Wada Y) Am J Hum Genet 1997 Mar;60(3):525-39 PMID: 9042911 PMCID: PMC1712531 SCOPUS ID: 2-s2.0-0031028360 03/01/1997       51 Citations
  • Pyrimidine metabolism in hereditary orotic aciduria. (Sumi S, Suchi M, Kidouchi K, Morishita H, Ohba S, Wada Y) J Inherit Metab Dis 1997 Mar;20(1):104-5 PMID: 9061575 SCOPUS ID: 2-s2.0-0031043601 03/01/1997       4 Citations
  • Microsatellite instability in in situ and invasive sporadic breast cancers of Japanese women. (Toyama T, Iwase H, Iwata H, Hara Y, Omoto Y, Suchi M, Kato T, Nakamura T, Kobayashi S) Cancer Lett 1996 Nov 29;108(2):205-9 PMID: 8973596 SCOPUS ID: 2-s2.0-0030606263 11/29/1996       21 Citations
  • Microsatellite instability in sporadic human breast cancers. (Toyama T, Iwase H, Yamashita H, Iwata H, Yamashita T, Ito K, Hara Y, Suchi M, Kato T, Nakamura T, Kobayashi S) Int J Cancer 1996 Nov 15;68(4):447-51 PMID: 8945614 SCOPUS ID: 2-s2.0-0029658742 11/15/1996       54 Citations
  • Identification and expression of a missense mutation (Y446C) in the acid sphingomyelinase gene from a Japanese patient with type A Niemann-Pick disease. (Takahashi T, Suchi M, Sato W, Ten SB, Sakuragawa N, Desnick RJ, Schuchman EH, Takada G) Tohoku J Exp Med 1995 Oct;177(2):117-23 PMID: 8693491 SCOPUS ID: 2-s2.0-0029386150 10/01/1995       7 Citations
  • Molecular cloning and structural characterization of the human histidase gene (HAL). (Suchi M, Sano H, Mizuno H, Wada Y) Genomics 1995 Sep 01;29(1):98-104 PMID: 8530107 SCOPUS ID: 2-s2.0-0029151627 09/01/1995       38 Citations
  • Molecular cloning of a cDNA encoding human histidase. (Suchi M, Harada N, Wada Y, Takagi Y) Biochim Biophys Acta 1993 Nov 16;1216(2):293-5 PMID: 7916645 SCOPUS ID: 2-s2.0-0027496435 11/16/1993       24 Citations
  • Toward gene therapy for Niemann-Pick disease (NPD): separation of retrovirally corrected and noncorrected NPD fibroblasts using a novel fluorescent sphingomyelin. (Dinur T, Schuchman EH, Fibach E, Dagan A, Suchi M, Desnick RJ, Gatt S) Hum Gene Ther 1992 Dec;3(6):633-9 PMID: 1482703 SCOPUS ID: 2-s2.0-0027021259 12/01/1992       15 Citations
  • Identification and expression of five mutations in the human acid sphingomyelinase gene causing types A and B Niemann-Pick disease. Molecular evidence for genetic heterogeneity in the neuronopathic and non-neuronopathic forms. (Takahashi T, Suchi M, Desnick RJ, Takada G, Schuchman EH) J Biol Chem 1992 Jun 25;267(18):12552-8 PMID: 1618760 SCOPUS ID: 2-s2.0-0026622926 06/25/1992       51 Citations
  • Retroviral-mediated transfer of the human acid sphingomyelinase cDNA: correction of the metabolic defect in cultured Niemann-Pick disease cells. (Suchi M, Dinur T, Desnick RJ, Gatt S, Pereira L, Gilboa E, Schuchman EH) Proc Natl Acad Sci U S A 1992 Apr 15;89(8):3227-31 PMID: 1565614 PMCID: PMC48839 SCOPUS ID: 2-s2.0-0026607916 04/15/1992       29 Citations
  • An MspI polymorphism in the human acid sphingomyelinase gene (SMPD1). (Schuchman EH, Levran O, Suchi M, Desnick RJ) Nucleic Acids Res 1991 Jun 11;19(11):3160 PMID: 1711683 PMCID: PMC328296 SCOPUS ID: 2-s2.0-0025822034 06/11/1991       11 Citations
  • Human acid sphingomyelinase. Isolation, nucleotide sequence and expression of the full-length and alternatively spliced cDNAs. (Schuchman EH, Suchi M, Takahashi T, Sandhoff K, Desnick RJ) J Biol Chem 1991 May 05;266(13):8531-9 PMID: 1840600 SCOPUS ID: 2-s2.0-0025819971 05/05/1991       200 Citations
  • Isolation of cDNA clones encoding human acid sphingomyelinase: occurrence of alternatively processed transcripts. (Quintern LE, Schuchman EH, Levran O, Suchi M, Ferlinz K, Reinke H, Sandhoff K, Desnick RJ) EMBO J 1989 Sep;8(9):2469-73 PMID: 2555181 PMCID: PMC401234 SCOPUS ID: 2-s2.0-0024423426 09/01/1989       134 Citations
  • Molecular cloning of human UMP synthase. (Suchi M, Harada N, Tsuboi T, Asai K, Okajima K, Wada Y, Takagi Y) Adv Exp Med Biol 1989;253A:511-8 PMID: 2624233 SCOPUS ID: 2-s2.0-0024824453 01/01/1989       3 Citations
  • A screening method for dihydropyrimidine dehydrogenase deficiency with colorimetric detection of urinary uracil. (Okajima K, Yamamoto T, Suchi M, Wada Y) Adv Exp Med Biol 1989;253A:119-22 PMID: 2624179 SCOPUS ID: 2-s2.0-0024824451 01/01/1989       1 Citation
  • Bioavailability of a film-coated tablet of valproate in nonfasting volunteers. (Ishikawa T, Horie M, Furuyama M, Ohuchi M, Awaya A, Sobajima H, Suchi M, Yamaguchi A, Okajima K, Wanibe M) Jpn J Psychiatry Neurol 1987 Dec;41(4):693-8 PMID: 3134567 SCOPUS ID: 2-s2.0-0023623768 12/01/1987       5 Citations
  • Increase of protein synthesis by uridine supplement in lectin-stimulated peripheral blood lymphocytes and EB virus-transformed B cell line of hereditary orotic aciduria type I. (Yazaki M, Okajima K, Suchi M, Morishita H, Wada Y) Tohoku J Exp Med 1987 Nov;153(3):189-95 PMID: 2829387 SCOPUS ID: 2-s2.0-0023551459 11/01/1987       4 Citations
    • Last update: 08/06/2022