Baylor College of Medicine Internal Medicine/Medical Genetics and Genomics

Residency · Houston, TX

Sponsored by Baylor College of Medicine · Director Reid Sutton

Reid Sutton, MD
Program Director
Clinical biochemical genetics physician, Professor at Baylor College of Medicine
Osteogenesis imperfecta/brittle bone disease, Achondroplasia, Creatine transporter deficiency, Aicardi syndrome
April Adams, MD, MS
Assistant Professor
Obstetrician-gynecologist, Assistant Professor of Obstetrics & Gynecology at Baylor College of Medicine
Brendan Lee, MD, PhD
Chair
Clinical biochemical genetics physician, Chair at Baylor College of Medicine
Developmental, translational and clinical studies of skeletal dysplasias and inborn errors of metabolism
Bridget Kiely, MD
Resident
Internal Medicine resident, Baylor College of Medicine
Carlos Bacino, MD
Professor
Clinical cytogenetics and genomics physician, Chief at Baylor College of Medicine
Clinical studies in patients with imprinting disorders (Angelman Syndrome), skeletal dysplasias, and genomic disorders
Charlene Radler, MD
Resident
Internal Medicine resident, Baylor College of Medicine
Chaya Murali, MD
Assistant Professor
Pediatrician, Assistant Professor of Molecular & Human Genetics at Baylor College of Medicine
Christine Eng, MD
Professor
Medical genetics and genomics physician, Professor at Baylor College of Medicine
Genetic testing for inherited diseases, Natural history, molecular genetics, and treatment of lysosomal storage disorders
Daryl Scott, MD, PhD
Professor
Medical genetics / clinical genetics (m.d.) physician, Professor at Baylor College of Medicine
Identifying and characterizing genes responsible for common birth defects
Evan Schauer, MD
Physician
Internist at Mary Washington Hospital
Fernando Scaglia, MD
Professor
Clinical genetics and genomics physician, Professor at Baylor College of Medicine
Mitochondrial cytopathies, other inborn errors of metabolism, Molecular bases of pediatric mitochondrial encephalomyopathies, Stable isotope studies in MELAS syndrome to evaluate nitric oxide flux production and glucose kinetics, EPI-746 clinical trial for Leigh syndrome
Gregory Boyek, MD, MSE
Resident
Internal Medicine resident, Baylor College of Medicine
Ignatia Van den Veyver, MD
Henry and Emma Meyer Chair and Professor
Obstetrician-gynecologist, Henry and Emma Meyer Chair and Professor at Baylor College of Medicine
Genetics and epigenetics of reproductive disorders; Aicardi syndrome; prenatal gene-environment interactions; prenatal genetics
Keren Machol, MD, PhD
Assistant Professor
Clinical genetics and genomics physician, Assistant Professor at Baylor College of Medicine
Kevin Glinton, MD, PhD
Assistant Professor
Clinical genetics and genomics physician, Assistant Professor at Baylor College of Medicine
Laurie Robak, MD, PhD
Assistant Professor
Clinical genetics and genomics physician, Assistant Professor at Baylor College of Medicine
Genetics of Parkinson's disease, Lysosomal storage disorders, Genetics of neurodegenerative diseases
Lilei Zhang, MD, PhD
Associate Professor
Clinical genetics and genomics physician, Associate Professor at Baylor College of Medicine
Genetic and Epigenetic regulation of heart failure and cardiomyopathies, Investigate the pathogenesis and treatment for inherited cardiac diseases using iPSC-CM model
Lindsay Burrage, MD, PhD
Associate Professor
Medical genetics / clinical genetics (m.d.) physician, Associate Professor at Baylor College of Medicine
Inborn errors of metabolism, skeletal dysplasia, pediatric genetics, undiagnosed genetic disorders, Molecular Genetics and Metabolism, . 21:1977-1986.
Lorraine Potocki, MD
Professor
Pediatric Pathology fellow, Alpert Medical School
Michael Wangler, MD
Associate Professor
Medical genetics / clinical genetics (m.d.) physician, Associate Professor at Baylor College of Medicine
Molecular and Developmental Mechanisms of Mendelian Disorders, Pediatric genetics, Peroxisomal disorders
Monika Weisz-Hubshman, MD, PhD
Assistant Professor
Medical genetics / clinical genetics (m.d.) physician, Assistant Professor at Baylor College of Medicine
Undiagnosed rare genetic disorders, Cartilage and bone disorders; neurodevelopmental disorders
Ronit Marom, MD, PhD
Assistant Professor
Clinical genetics and genomics physician, Assistant Professor at Baylor College of Medicine
Pediatric genetics, Inborn errors of metabolism, Undiagnosed genetic disorders, Cell Rep
Sandesh Nagamani, MD, MBBS
Professor
Clinical genetics and genomics physician, Professor at Baylor College of Medicine
Sanmati Cuddapah, MD
Associate Professor
Clinical genetics and genomics physician, Associate Professor at Baylor College of Medicine
Inherited Metabolic Disorders, Williams Syndrome, Collaborative Registry for Williams Syndrome (CReWS), Priestley JRC, Pace LM, Sen K, Aggarwal A, Alves CAPF, Campbell IM

Reid Sutton, MD
Program Director
Clinical biochemical genetics physician, Professor at Baylor College of Medicine
Osteogenesis imperfecta/brittle bone disease, Achondroplasia, Creatine transporter deficiency, Aicardi syndrome
April Adams, MD, MS
Assistant Professor
Obstetrician-gynecologist, Assistant Professor of Obstetrics & Gynecology at Baylor College of Medicine
Brendan Lee, MD, PhD
Chair
Clinical biochemical genetics physician, Chair at Baylor College of Medicine
Developmental, translational and clinical studies of skeletal dysplasias and inborn errors of metabolism
Bridget Kiely, MD
Resident
Internal Medicine resident, Baylor College of Medicine
Carlos Bacino, MD
Professor
Clinical cytogenetics and genomics physician, Chief at Baylor College of Medicine
Clinical studies in patients with imprinting disorders (Angelman Syndrome), skeletal dysplasias, and genomic disorders
Charlene Radler, MD
Resident
Internal Medicine resident, Baylor College of Medicine
Chaya Murali, MD
Assistant Professor
Pediatrician, Assistant Professor of Molecular & Human Genetics at Baylor College of Medicine
Christine Eng, MD
Professor
Medical genetics and genomics physician, Professor at Baylor College of Medicine
Genetic testing for inherited diseases, Natural history, molecular genetics, and treatment of lysosomal storage disorders
Daryl Scott, MD, PhD
Professor
Medical genetics / clinical genetics (m.d.) physician, Professor at Baylor College of Medicine
Identifying and characterizing genes responsible for common birth defects
Evan Schauer, MD
Physician
Internist at Mary Washington Hospital
Fernando Scaglia, MD
Professor
Clinical genetics and genomics physician, Professor at Baylor College of Medicine
Mitochondrial cytopathies, other inborn errors of metabolism, Molecular bases of pediatric mitochondrial encephalomyopathies, Stable isotope studies in MELAS syndrome to evaluate nitric oxide flux production and glucose kinetics, EPI-746 clinical trial for Leigh syndrome
Gregory Boyek, MD, MSE
Resident
Internal Medicine resident, Baylor College of Medicine
Ignatia Van den Veyver, MD
Henry and Emma Meyer Chair and Professor
Obstetrician-gynecologist, Henry and Emma Meyer Chair and Professor at Baylor College of Medicine
Genetics and epigenetics of reproductive disorders; Aicardi syndrome; prenatal gene-environment interactions; prenatal genetics
Keren Machol, MD, PhD
Assistant Professor
Clinical genetics and genomics physician, Assistant Professor at Baylor College of Medicine
Kevin Glinton, MD, PhD
Assistant Professor
Clinical genetics and genomics physician, Assistant Professor at Baylor College of Medicine
Laurie Robak, MD, PhD
Assistant Professor
Clinical genetics and genomics physician, Assistant Professor at Baylor College of Medicine
Genetics of Parkinson's disease, Lysosomal storage disorders, Genetics of neurodegenerative diseases
Lilei Zhang, MD, PhD
Associate Professor
Clinical genetics and genomics physician, Associate Professor at Baylor College of Medicine
Genetic and Epigenetic regulation of heart failure and cardiomyopathies, Investigate the pathogenesis and treatment for inherited cardiac diseases using iPSC-CM model
Lindsay Burrage, MD, PhD
Associate Professor
Medical genetics / clinical genetics (m.d.) physician, Associate Professor at Baylor College of Medicine
Inborn errors of metabolism, skeletal dysplasia, pediatric genetics, undiagnosed genetic disorders, Molecular Genetics and Metabolism, . 21:1977-1986.
Lorraine Potocki, MD
Professor
Pediatric Pathology fellow, Alpert Medical School
Michael Wangler, MD
Associate Professor
Medical genetics / clinical genetics (m.d.) physician, Associate Professor at Baylor College of Medicine
Molecular and Developmental Mechanisms of Mendelian Disorders, Pediatric genetics, Peroxisomal disorders
Monika Weisz-Hubshman, MD, PhD
Assistant Professor
Medical genetics / clinical genetics (m.d.) physician, Assistant Professor at Baylor College of Medicine
Undiagnosed rare genetic disorders, Cartilage and bone disorders; neurodevelopmental disorders
Ronit Marom, MD, PhD
Assistant Professor
Clinical genetics and genomics physician, Assistant Professor at Baylor College of Medicine
Pediatric genetics, Inborn errors of metabolism, Undiagnosed genetic disorders, Cell Rep
Sandesh Nagamani, MD, MBBS
Professor
Clinical genetics and genomics physician, Professor at Baylor College of Medicine
Sanmati Cuddapah, MD
Associate Professor
Clinical genetics and genomics physician, Associate Professor at Baylor College of Medicine
Inherited Metabolic Disorders, Williams Syndrome, Collaborative Registry for Williams Syndrome (CReWS), Priestley JRC, Pace LM, Sen K, Aggarwal A, Alves CAPF, Campbell IM