Therese Gadomski, MD
Assistant Professor
Ob/Gyn, Reproductive Sciences
School of Medicine

Education & Training

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• Residency Obstetrics & Gynecology Zucker School of Medicine at Hofstra/Northwell at Lenox Hill 2021
• MD Medicine Tulane University School of Medicine 2017
• BS Biochemistry & Cell Biology University of California, San Diego 2010

Publications (9)

Top publication keywords:
Glycogen Storage DiseaseTransferrinCardiomyopathiesGlycosylationGene DuplicationMutationGalactoseCongenital Disorders of GlycosylationPregnancy Complications, InfectiousPregnancy Complications, CardiovascularIsoelectric FocusingSeizuresN-AcetylglucosaminyltransferasesCognitionMutation Rate

• Implementation of a Standardized Post-Cesarean Delivery Order Set with Multimodal Combination Analgesia Reduces Inpatient Opioid Usage.
  Journal of clinical medicine 2020 Bornstein E, Husk G, Lenchner E, Grunebaum A, Gadomski T, Zottola C, Werner S, Hirsch JS, Chervenak FA
• Myocardial injury associated with coronavirus disease 2019 in pregnancy.
  American journal of obstetrics and gynecology 2020 Pachtman Shetty SL, Meirowitz N, Blitz MJ, Gadomski T, Weinberg CR
• ALG13-CDG in a male with seizures, normal cognitive development, and normal transferrin isoelectric focusing.
  American journal of medical genetics. Part A 2017 Gadomski TE, Bolton M, Alfadhel M, Dvorak C, Ogunsakin OA, Nelson SL, Morava E
• Oral D-galactose supplementation in PGM1-CDG.
  Genetics in medicine : official journal of the American College of Medical Genetics 2017 Wong SY, Gadomski T, van Scherpenzeel M, Honzik T, Hansikova H, Holmefjord KSB, Mork M, Bowling F, Sykut-Cegielska J, Koch D, Hertecant J, Preston G, Jaeken J, Peeters N, Perez S, Nguyen DD, Crivelly …
• Galactose Supplementation in Patients With TMEM165-CDG Rescues the Glycosylation Defects.
  The Journal of clinical endocrinology and metabolism 2017 Morelle W, Potelle S, Witters P, Wong S, Climer L, Lupashin V, Matthijs G, Gadomski T, Jaeken J, Cassiman D, Morava E, Foulquier F

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• Defining the Phenotype and Assessing Severity in Phosphoglucomutase-1 Deficiency.
  The Journal of pediatrics 2016 Wong SY, Beamer LJ, Gadomski T, Honzik T, Mohamed M, Wortmann SB, Brocke Holmefjord KS, Mork M, Bowling F, Sykut-Cegielska J, Koch D, Ackermann A, Stanley CA, Rymen D, Zeharia A, Al-Sayed M, Marquardt…
• Frequency and Complexity of De Novo Structural Mutation in Autism.
  American journal of human genetics 2016 Brandler WM, Antaki D, Gujral M, Noor A, Rosanio G, Chapman TR, Barrera DJ, Lin GN, Malhotra D, Watts AC, Wong LC, Estabillo JA, Gadomski TE, Hong O, Fajardo KV, Bhandari A, Owen R, Baughn M, Yuan J, …
• Congenital disorders of glycosylation: new defects and still counting.
  Journal of inherited metabolic disease 2014 Scott K, Gadomski T, Kozicz T, Morava E
• Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.
  Cell 2012 Michaelson JJ, Shi Y, Gujral M, Zheng H, Malhotra D, Jin X, Jian M, Liu G, Greer D, Bhandari A, Wu W, Corominas R, Peoples A, Koren A, Gore A, Kang S, Lin GN, Estabillo J, Gadomski T, Singh B, Zhang K…