RichardJSchroerMD

Medical Genetics • North Charleston, SC

Clinical Biochemical Genetics, Clinical Genetics

Physician

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Office
3520 W Montague Ave Ste 104
North Charleston, SC 29418
Phone+1 843-746-1001

Fax+1 843-746-1002
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Summary

Dr. Richard Schroer, MD is a board certified medical geneticist in North Charleston, South Carolina. He is currently licensed to practice medicine in South Carolina and North Carolina. He is affiliated with Prisma Health Richland Hospital.

Education & Training

Wake Forest University School of MedicineResidency, Pediatrics, 1976 - 1978
Wake Forest University School of MedicineInternship, Pediatrics, 1975 - 1976
Wake Forest School of Medicine of Wake Forest Baptist Medical CenterClass of 1975

Certifications & Licensure

SC State Medical License 1978 - 2025
NC State Medical License 1975 - 2002
American Board of Medical Genetics and Genomics Clinical Biochemical Genetics
American Board of Medical Genetics and Genomics Clinical Genetics
American Board of Pediatrics Pediatrics

Publications & Presentations

PubMed

5 citations
Autistic Disorder: A 20 Year Chronicle.
Cindy Skinner, Rini Pauly, Steven A. Skinner, Richard J. Schroer, Richard J. Simensen, Harold A. Taylor, Michael J. Friez, Barbara R. DuPont, Roger E. Stevenson> ;Journal of Autism and Developmental Disorders. 2021 Feb 1
Clinical utility of the X-chromosome array
Yuri A. Zarate, Alka Dwivedi, Frank O. Bartel, M. Allison Bellomo, Sara S. Cathey, Neena L. Champaigne, L. Kate Clarkson, Barbara R. DuPont, David B. Everman, Joseph S...> ;American Journal of Medical Genetics. Part A. 2013 Jan 1
163 citations
Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders.
Luigi Boccuto, Maria Lauri, Sara M. Sarasua, Cindy Skinner, Daniela Buccella, Alka Dwivedi, Daniela Orteschi, Julianne S. Collins, Marcella Zollino, Paola Visconti, Ba...> ;European Journal of Human Genetics. 2013 Mar 1
10 citations
Duplication of OCRL and adjacent genes associated with autism but not Lowe syndrome.
Richard J. Schroer, Arthur L. Beaudet, Marwan Shinawi, Trilochan Sahoo, Ankita Patel, Qin Sun, Cindy Skinner, Roger E. Stevenson> ;American Journal of Medical Genetics. Part A. 2012 Oct 1
97 citations
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism
Patrícia B. S. Celestino-Soper, Sara Violante, Emily L. Crawford, Rui Luo, Anath C. Lionel, Elsa Delaby, Guiqing Cai, Bekim Sadikovic, Kwanghyuk Lee, Charlene Lo, Kun ...> ;Proceedings of the National Academy of Sciences of the United States of America. 2012 May 22
37 citations
Deletions in chromosome 6p22.3-p24.3, including ATXN1 , are associated with developmental delay and autism spectrum disorders
Patrícia B. S. Celestino-Soper, Cindy Skinner, Richard J. Schroer, Patricia A. Eng, Jayant P. Shenai, Malgorzata M.J. Nowaczyk, Deborah Terespolsky, Donna Cushing, Gay...> ;Molecular Cytogenetics. 2012 Apr 5
21 citations
Two patients with hepatic mtDNA depletion syndromes and marked elevations of S-adenosylmethionine and methionine.
S. Harvey Mudd, Conrad Wagner, Zigmund Luka, Sally P. Stabler, Robert H. Allen, Richard J. Schroer, Tim Wood, Jing Wang, Lee-Jun C. Wong> ;Molecular Genetics and Metabolism. 2012 Feb 1
22 citations
Primary Carnitine Deficiency Presents Atypically with Long QT Syndrome: A Case Report.
Irene De Biase, Neena L. Champaigne, Richard J. Schroer, Laura M. Pollard, Nicola Longo, Tim Wood> ;JIMD Reports. 2011 Jan 1
56 citations
Natural history of Christianson syndrome.
Richard J. Schroer, Kenton R. Holden, Patrick S. Tarpey, Maria Giselle Matheus, David A. Griesemer, Michael J. Friez, Jane Zheng Fan, Richard J. Simensen, Petter Strøm...> ;American Journal of Medical Genetics. Part A. 2010 Nov 1
18 citations
Diagnosis, Treatment, and Long-Term Outcomes of Late-Onset (Type III) Multiple Acyl-CoA Dehydrogenase Deficiency
Laura Pollard, Nolan R. Williams, Lesby Espinoza, Tim Wood, Elaine B. Spector, Richard J. Schroer, Kenton R. Holden> ;Journal of Child Neurology. 2010 Aug 1
90 citations
Alterations in CDH15 and KIRREL3 in Patients with Mild to Severe Intellectual Disability
Kavita Bhalla, Yue Luo, Tim Buchan, Michael A. Beachem, Gregory F. Guzauskas, Sydney Ladd, Shelly J. Bratcher, Richard J. Schroer, Janne Balsamo, Barbara R. DuPont, Ja...> ;American Journal of Human Genetics. 2008 Dec 12
58 citations
Analysis of the neuroligin 4Y gene in patients with autism.
Jin Yan, Jinong Feng, Richard J. Schroer, Wenyan Li, Cindy Skinner, Charles E. Schwartz, Edwin H. Cook, Steve S. Sommer> ;Psychiatric Genetics. 2008 Aug 1
17 citations
Nonsyndromic X-linked mental retardation: review and mapping of MRX29 to Xp21.
Bernhard Hane, Richard J. Schroer, J F Arena, Herbert A. Lubs, Charles E. Schwartz, Roger E. Stevenson> ;Clinical Genetics. 2008 Jun 28
112 citations
Neurexin 1α structural variants associated with autism
Jin Yan, Katie Noltner, Jinong Feng, Wenyan Li, Richard J. Schroer, Cindy Skinner, Wenqi Zeng, Charles E. Schwartz, Steve S. Sommer> ;Neuroscience Letters. 2008 Jun 27
16 citations
Duplication-deletion syndrome in a family with pericentric inversion of chromosome 6.
Richard J. Schroer, Donna M. Culp, Roger E. Stevenson, William E. Potts, Harold A. Taylor, Richard J. Simensen> ;Clinical Genetics. 2008 Apr 23
421 citations
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.
Andrew J. Sharp, Heather C Mefford, Kelly Li, Carl Baker, Cindy Skinner, Roger E. Stevenson, Richard J. Schroer, Francesca Novara, Manuela De Gregori, Roberto Ciccone,...> ;Nature Genetics. 2008 Mar 1
68 citations
Expanded newborn screening identifies maternal primary carnitine deficiency.
Lisa A. Schimmenti, Eric Crombez, Bernd Schwahn, Bryce A. Heese, Tim Wood, Richard J. Schroer, Kristi Bentler, Stephen D. Cederbaum, Kyriakie Sarafoglou, Mark McCann, ...> ;Molecular Genetics and Metabolism. 2007 Apr 1
240 citations
High frequency of neurexin 1beta signal peptide structural variants in patients with autism
Steve S. Sommer, Jinong Feng, Jin Yan> ;Neuroscience Letters. 2007 Sep 21
55 citations
Epimerase-Deficiency Galactosemia Is Not a Binary Condition
Kimberly K. Openo, Jenny M. Schulz, Claudia A. Vargas, Corey S. Orton, Michael P. Epstein, Rhonda E. Schnur, Fernando Scaglia, Gerard T. Berry, Gary S. Gottesman, Can ...> ;American Journal of Human Genetics. 2006 Jan 1
38 citations
Array-based comparative genomic hybridization analysis of recurrent chromosome 15q rearrangements.
Trilochan Sahoo, Chad A. Shaw, Andrew S. Young, Nathan L. Whitehouse, Richard J. Schroer, Roger E. Stevenson, Arthur L. Beaudet> ;American Journal of Medical Genetics. Part A. 2005 Dec 1
107 citations
A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A.
Yong-hui Jiang, Trilochan Sahoo, Ron C. Michaelis, Dani Bercovich, Jan Bressler, Catherine D. Kashork, Qian Liu, Lisa G. Shaffer, Richard J. Schroer, David W. Stockton...> ;American Journal of Medical Genetics. Part A. 2004 Nov 15
31 citations
Genetic syndromes among individuals with mental retardation.
Roger E. Stevenson, Ashley M. Procopio-Allen, Richard J. Schroer, Julianne S. Collins> ;American Journal of Medical Genetics. Part A. 2003 Nov 15
12 citations
The HOXA1 A218G polymorphism and autism: lack of association in white and black patients from the South Carolina Autism Project.
Julianne S. Collins, Richard J. Schroer, Jeffrey Bird, Ron C. Michaelis> ;Journal of Autism and Developmental Disorders. 2003 Jun 1
39 citations
Absence of MeCP2 mutations in patients from the South Carolina autism project
Fe Lobo-Menendez, Khalid Sossey-Alaoui, Jennifer M. Bell, Susan A. Copeland-Yates, Sara M. Plank, Stewart O. Sanford, Cindy Skinner, Richard J. Simensen, Richard J. Sc...> ;American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics. 2003 Feb 15
37 citations
Genomic rearrangements of EYA1 account for a large fraction of families with BOR syndrome
Virginie S. Vervoort, Richard J.H. Smith, Jane E. O'Brien, Richard J. Schroer, Albert G. Abbott, Roger E. Stevenson, Charles E. Schwartz> ;European Journal of Human Genetics. 2002 Nov 1
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Hospital Affiliations

Prisma Health Richland HospitalColumbia, South Carolina