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Faculty, UW–Madison


ROBERT STEINER, MD

 * Pediatric Genetics and Metabolism


About
Practice locations
Education & credentials
Areas of expertise
Research & publications
Robert Steiner
About
Practice locations
Education & credentials
Areas of expertise
Research & publications
 
More
+
About
Practice locations
Education & credentials
Areas of expertise
Research & publications


ABOUT



Dr. Steiner has a longstanding interest and expertise in biochemical genetic
disorders, including those affecting bone metabolism. Steiner is a graduate of
the University of Wisconsin and was awarded an MD from the University of
Wisconsin School of Medicine and Public Health (formerly UW Medical School),
Madison, WI. He completed residency in pediatrics at Cincinnati Children’s
Hospital Medical Center and fellowship in medical genetics at the University of
Washington and Seattle Children’s Hospital Regional Medical Center. Dr. Steiner
is board certified in pediatrics, clinical genetics, and clinical biochemical
genetics, and is a member of the faculty of the Division of Genetics and
Metabolism. 



Dr. Steiner is an active pediatric genetics clinician, with particular interests
in pediatric metabolic bone diseases, inherited metabolic diseases, lysosomal
storage diseases, cholesterol disorders, and newborn screening.

Languages spoken
 * English

University affiliation
 * Department of Pediatrics


PRACTICE LOCATIONS




 * AMERICAN FAMILY CHILDREN'S HOSPITALPEDIATRIC BONE AND MINERAL METABOLISM
   CLINIC
   
   
    * 1675 Highland Ave / Madison, WI
    * (608) 263-6420
    * 


EDUCATION & CREDENTIALS


Board certifications
 * Clinical Biochemical Genetics
 * Clinical Genetics and Genomics
 * Pediatrics

Medical School
 * University of Wisconsin School of Medicine and Public Health (formerly UW
   Medical School), Madison, WI

Fellowships
 * University of Washington Medical Center, Seattle, WA

Residencies
 * Children's Hospital Medical Center, Cincinnati, OH


AREAS OF EXPERTISE


 * Cystinosis
 * Fibrodysplasia Ossificans Progressiva
 * Hypophosphatasia
 * Hypophosphatemic Rickets
 * Low Bone Mineral Density in Children
 * Lysosomal Storage Disorders
 * Osteogenesis Imperfecta
 * Osteopetrosis
 * Pediatric genetic specialists
 * Rickets (Vitamin D Deficiency)
 * Smith-Lemli-Opitz Syndrome


RESEARCH & PUBLICATIONS

Dr. Steiner has served as the Principal Investigator for more than a dozen
clinical trials and clinical research studies with continuous research funding
from the National Institutes of Health for nearly 20 years. He currently serves
as an editorial board member of the _Journal of Inherited Metabolic Disease and
New Horizons in Translational Medicine,_ and is Deputy Editor for
Nature/Springer Publishing’s _Genetics in Medicine_.


Published works (PubMed)

May 17, 2024
Implementing Evidence-Based Assertions of Clinical Actionability in the Context
of Secondary Findings: Updates from the ClinGen Actionability Working Group
May 06, 2024
It is Time to Screen for Homozygous Familial Hypercholesterolemia in the United
States
Mar 16, 2024
Quantifying preferences for urea cycle disorder treatments using a discrete
choice experiment
Mar 15, 2024
Guidance on Use of Race, Ethnicity, and Geographic Origin as Proxies for Genetic
Ancestry Groups in Biomedical Publications
Mar 14, 2024
Guidance on use of race, ethnicity, and geographic origin as proxies for genetic
ancestry groups in biomedical publications
Mar 13, 2024
Guidance on use of race, ethnicity, and geographic origin as proxies for genetic
ancestry groups in biomedical publications
Mar 13, 2024
Guidance on use of race, ethnicity, and geographic origin as proxies for genetic
ancestry groups in biomedical publications
Mar 12, 2024
Guidance on Use of Race, Ethnicity, and Geographic Origin as Proxies for Genetic
Ancestry Groups in Biomedical Publications
Jan 12, 2024
Identification of pathogenic genetic variants in patients with acquired
early-onset bilateral cataracts using next-generation sequencing
Dec 19, 2023
Living with Cerebrotendinous Xanthomatosis: Patient, Caregiver, and Expert
Perspectives
Jul 18, 2023
COL11A2 as a candidate gene for vertebral malformations and congenital scoliosis
Apr 02, 2023
Taste-masked formulation of sodium phenylbutyrate (ACER-001) for the treatment
of urea cycle disorders
Jan 17, 2023
Allelic prevalence and geographic distribution of cerebrotendinous xanthomatosis
Nov 14, 2022
Statins for Smith-Lemli-Opitz syndrome
Oct 04, 2022
Myhre syndrome is caused by dominant-negative dysregulation of SMAD4 and other
co-factors
Sep 14, 2022
Dental manifestations in adult hypophosphatasia and their correlation with
biomarkers
Mar 28, 2022
ClinGen's Pediatric Actionability Working Group: Clinical actionability of
secondary findings from genome-scale sequencing in children and adolescents
Feb 25, 2022
Real-world effectiveness of burosumab in children with X-linked hypophosphatemic
rickets
Dec 09, 2021
Remediation of <em>ABCG5</em>-Linked Macrothrombocytopenia With
Ezetimibe Therapy
Jan 01, 1993
<em>COL1A1/2</em> Osteogenesis Imperfecta
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