HansAnderssonMD(They/Them)
Medical Genetics • New Orleans, LAClinical Biochemical Genetics, Clinical Biochemical/Molecular Genetics, Clinical Genetics
Karen Gore Chair of Human Genetics, Professor of Pediatrics, Tulane University
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Office
1415 Tulane Ave
Tulane University Medical School
New Orleans, LA 70112Phone+1 504-988-2300Fax+1 504-988-8886
Summary
Education & Training
Georg-August University of Goettingen, GERMANYPost-Doctoral Fellowship, 1991 - 1993
National Institutes of Health Clinical CenterFellowship, Medical Genetics and Genomics, 1987 - 1991
Tulane UniversityResidency, Pediatrics, 1984 - 1987- Tulane University School of MedicineClass of 1984
Certifications & Licensure
LA State Medical License 1985 - 2024- American Board of Medical Genetics and Genomics Clinical Biochemical/Molecular Genetics
- American Board of Medical Genetics and Genomics Clinical Genetics
Awards, Honors, & Recognition
- Best Doctor US News & World Report, 2013-2021
- America's Top Doctors Castle Connolly, 2013-2021
- Super Doctor SuperDoctors.com
Clinical Trials
- Clinical and Basic Investigations Into Congenital Disorders of Glycosylation Start of enrollment: 2019 Oct 08
Publications & Presentations
PubMed
- Outcomes in 14 live births resulting from Pegvaliase-treated pregnancies in PKU-affected females.Caide Bier, Kaelin Dickey, Brittan Bibb, Angela Crutcher, Rebecca Sponberg
Molecular Genetics and Metabolism. 2024-03-01 - 2 citationsMaximal dietary responsiveness after tetrahydrobiopterin (BH4) in 19 phenylalanine hydroxylase deficiency patients: What super-responders can expect.Jariya Upadia, Kea Crivelly, Grace Noh, Amy Cunningham, Caroline Cerminaro
Molecular Genetics and Metabolism Reports. 2024-03-01 - 1 citationsBiochemical and molecular characteristics among infants with abnormal newborn screen for very-long-chain acyl-CoA dehydrogenase deficiency: A single center experience.Jariya Upadia, Grace Noh, John J Lefante, Hans C Andersson
Molecular Genetics and Metabolism Reports. 2023-12-01
Other
- A SUCLG1 Mutation in a patient with mitochondrial DNA Depletion and Congenital AnomaliesML Landsverk, VW Zhang, LC Wong, HC Andersson, Molec Gen Metab Rep
http://authors.elsevier.com/sd/article/S2214426914000652
2014
Press Mentions
ONE OF MY TOUGHEST CASES: The Missing EnzymeAugust 12th, 2015
Committees
- Residency Review Comm Member: Medical Genetics, Molecular Genetics Pathology, 2012-2017, Accreditation Council of Graduate Medical Education
Professional Memberships
- American College of Medical Genetics and GenomicsMember
- Society of Inherited Metabolic DiseasesMember
- Society for Pediatric ResearchMember
Other Languages
- German
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