25 of the Best Geneticists Near Me

Richard Rogers is a Medical Genetics provider practicing medicine in Greenville, South Carolina. His clinical expertise encompasses Macroglossia, Beckwith-Wiedemann Syndrome, and Autosomal Cleft Palate. Dr. Rogers is currently accepting new patients.

Sara Pajouhanfar is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Great Neck, New York. Her clinical expertise encompasses Liver Failure.

Steven Bleyl is a Medical Genetics provider practicing medicine in Salt Lake City, Utah. His clinical expertise encompasses Agyria Pachygyria Polymicrogyria. Dr. Bleyl is board certified in American Board Of Medical Genetics & Genomics. Dr. Bleyl is currently accepting new patients.

Robert Slotnick is a Medical Genetics specialist and an Obstetrics and Gynecologist practicing medicine in Reno, Nevada.

Erin Cooney is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Galveston, Texas. Dr. Cooney is highly rated in 99 conditions, according to our data. Her clinical expertise encompasses Delayed Growth, Lacrimo-Auriculo-Dento-Digital Syndrome, Caudal Appendage Deafness, and Acrorenal Mandibular Syndrome.

Dr. Natalie M. Gallant is a board-certified UCI Health physician who specializes in clinical genetics and medical biochemical genetics.She provides diagnostic evaluations for newborns and children who are affected by a broad range of genetic conditions at the Stramski Children’s Development Center at Miller Children’s Hospital of Long Beach. These include birth defects, connective tissue disorders, developmental impairment, neurological disorders and skeletal dysplasia.Gallant earned her medical degree at Keck School of Medicine at the University of Southern California in Los Angeles. She completed an internship and a residency in pediatrics and medical genetics with the UCLA Intercampus Medical Genetics Training Program. She also completed a fellowship in medical biochemical genetics with the program, which is jointly run by UCLA, Cedars-Sinai Medical Center, Harbor-UCLA Medical Center and CHOC Children’s Hospital in Orange.Gallant’s research emphasis is in the field of inborn errors of metabolism, especially in urea cycle disorders in children and adults. Dr. Gallant is highly rated in 98 conditions, according to our data. Her clinical expertise encompasses Chromosome 8p Deletion, Chromosome 6q Duplication, Microcephaly, and Microcephaly Deafness Syndrome. Dr. Gallant is board certified in American Board Of Medical Genetics And Genomics - Clinical Genetics And Genomics.

Joseph Ray is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Galveston, Texas. Dr. Ray is highly rated in 95 conditions, according to our data. His clinical expertise encompasses Maternal Hyperphenylalaninemia, Phenylketonuria (PKU), Dihydropteridine Reductase Deficiency, and Fabry Disease.

Nina Powell is a Medical Genetics provider practicing medicine in Wilmington, Delaware. She has been practicing medicine for over 30 years. Dr. Powell is highly rated in 45 conditions, according to our data. Her clinical expertise encompasses Microcephaly, PIK3CA-Related Overgrowth Spectrum, Chromosome 13q Deletion, and Increased Head Circumference. Dr. Powell is board certified in American Board Of Medical Genetics And Genomics.

Andrea Petersen is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Portland, Oregon. Dr. Petersen is highly rated in 94 conditions, according to our data. Her clinical expertise encompasses Neu Laxova Syndrome, Blepharocheilodontic Syndrome, Manitoba Oculotrichoanal Syndrome, and Cardiomyopathy Hypogonadism Metabolic Anomalies.

Leslie Raffel is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Orange, California. Dr. Raffel is highly rated in 92 conditions, according to our data. Her clinical expertise encompasses Chromosome 13q Deletion, Smith-Magenis Syndrome, Miller-Dieker Syndrome, and HNRNPH2-Related Disorder. Dr. Raffel is board certified in American Board Of Pediatrics - Pediatrics.

David Stevenson is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Palo Alto, California. Dr. Stevenson is highly rated in 88 conditions, according to our data. His clinical expertise encompasses Neurofibromatosis, Neurofibromatosis Type 1 (NF1), Cardiomyopathic Lentiginosis, and Noonan Syndrome.

Mafalda Cabral-Dos is a Medical Genetics provider practicing medicine in New York, New York. Dr. Cabral-Dos is highly rated in 88 conditions, according to our data. Her clinical expertise encompasses Oculodentodigital Dysplasia, Woodhouse-Sakati Syndrome, Lacrimo-Auriculo-Dento-Digital Syndrome, and Nicolaides-Baraitser Syndrome.

Mindy Li is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Chicago, Illinois. She has been practicing medicine for over 17 years. Dr. Li is highly rated in 87 conditions, according to our data. Her clinical expertise encompasses Delayed Growth, Isolated Ectopia Lentis, Koolen De Vries Syndrome, and Costello Syndrome. Dr. Li is currently accepting new patients in some locations.

Rosemarie Smith is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Portland, Maine. Dr. Smith is highly rated in 86 conditions, according to our data. Her clinical expertise encompasses RASopathies, Cardiomyopathic Lentiginosis, Costello Syndrome, and Leber Hereditary Optic Neuropathy (LHON).

Jeremy Woods is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Los Angeles, California. Dr. Woods is highly rated in 80 conditions, according to our data. His clinical expertise encompasses Athabaskan Brain Stem Dysgenesis, Cockayne Syndrome Type 2, Branchiootorenal Syndrome, Filippi Syndrome, and Deep Brain Stimulation.

Walla Al-Hertani is a Medical Genetics provider practicing medicine in Orange, California. Dr. Al-Hertani is highly rated in 62 conditions, according to our data. Her clinical expertise encompasses Von Gierke Disease, Classic Galactosemia, Glycogen Storage Disease Type 7, and Andersen Disease. Dr. Al-Hertani is currently accepting new patients.

Sarah Little is a Medical Genetics provider practicing medicine in Wilmington, Delaware. Dr. Little is highly rated in 11 conditions, according to our data. Her clinical expertise encompasses Hypochondroplasia, Thanatophoric Dysplasia, Kozlowski Warren Fisher Syndrome, and Kozlowski Spondylometaphyseal Dysplasia. Dr. Little is board certified in National Commission On Certification Of Physician Assistants.

Dr. Stephen Braddock provides genetic evaluations, diagnoses, and counseling for patients of all ages. This includes services not exclusive to pediatric patients, but also prenatal counseling, cancer counseling, and adult genetic disorders. He specializes in delineation of new multiple malformation syndromes, dysmorphology, prevalence and variation of prenatal teratogen exposures and birth defects, and fetal alcohol syndrome. His research interests include teratology, fetal alcohol syndrome, and dysmorphology/syndrome delineation. Dr. Braddock is director of medical genetics and a professor in the Department of Pediatrics, Division of Medical Genetics, at Saint Louis University School of Medicine. He is a fellow of the American College of Medical Genetics and Genomics, and the American Academy of Pediatrics. He is a member of the American Society of Human Genetics, the Teratology Society, and the Organization of Teratogen Information Services. Dr. Braddock is a sports history/trivia buff, particularly baseball history. He owns two Babe Ruth baseball cards. Dr. Braddock is highly rated in 9 conditions, according to our data. His clinical expertise encompasses Chromosome 20 Trisomy, Cerebellar Hypoplasia, Coloboma, and CHARGE Syndrome. Dr. Braddock is board certified in American Board Of Medical Genetics & Genomics , American Board Of Pediatrics , Drug Enforcement Administration , Illinois Department Of Financial & Professional Regulation , Missouri Dept Of Health/Narcotics&Dangerous Drugs , and Missouri State Board Of Registration.

Dr. Joseph Shieh specializes in evaluating complex medical problems of unknown cause as well as inherited disorders. He focuses on rare diseases and syndromes that have components of common disorders, including birth defects, heart disease and brain disorders. He is experienced in providing personalized care to children, adults and families. As a member of the UCSF Institute for Human Genetics, Shieh combines state-of-the-art technology with discovery-based research to decipher how genetics impacts health. His overarching goal is to bring patients the best possible outcomes by emphasizing diagnostic precision, preventive medicine and comprehensive care. Shieh completed his undergraduate studies at Stanford University. He earned his medical degree from the Perelman School of Medicine at the University of Pennsylvania, where he also received his doctoral degree. He completed his residency in pediatrics at Seattle Children's Hospital, an affiliate of the University of Washington. After completing a fellowship in medical genetics at Stanford University, he joined UCSF. Shieh is a member of the American Society of Human Genetics. His work has received support from the National Heart, Lung, and Blood Institute, which is part of the National Institutes of Health. Dr. Shieh is highly rated in 7 conditions, according to our data. His clinical expertise encompasses Myhre Syndrome, Neurofibromatosis Type 1 (NF1), Neurofibromatosis, and Ectodermal Dysplasias. Dr. Shieh is board certified in American Board Of Medical Genetics And Genomics, Clinical Genetics And Genomics. Dr. Shieh is currently accepting new patients.

Zhenya Tang is a Medical Genetics provider practicing medicine in Omaha, Nebraska. He has been practicing medicine for over 37 years. Dr. Tang is highly rated in 6 conditions, according to our data. His clinical expertise encompasses Smoldering Multiple Myeloma, Small Lymphocytic Lymphoma (SLL), T-Cell Lymphoma, Osteotomy, and Splenectomy.

Peter Hulick, MD, a clinical geneticist and chair of personalized medicine at Endeavor Health, helps patients understand how genomic information can inform care and improve health outcomes. With a career rooted in genetics since high school, he works to integrate genomic data into everyday decision-making for patients and clinicians. Dr. Hulick focuses on risk assessment, early detection and treatment guidance by combining science, patient context and team collaboration. He also leads efforts to make genomic care more accessible across the health system. Dr. Hulick is highly rated in 5 conditions, according to our data. His clinical expertise encompasses Ehlers-Danlos Syndrome (EDS), Retinopathy Pigmentary Mental Retardation, BRCA Positive Breast Cancer, and Li-Fraumeni Syndrome. Dr. Hulick is board certified in American Board Of Internal Medicine and American Board Of Medical Genetics.

Dr. Natalie Hauser is a specialty care physician board certified in clinical and biochemical genetics at Inova Health System. She joined Inova in 2015 and has been practicing since 2010. Prior to joining Inova, Dr. Hauser worked as a clinical geneticist in Fresno, CA. Dr. Hauser is highly rated in 5 conditions, according to our data. Her clinical expertise encompasses Focal or Multifocal Malformations in Neuronal Migration, Increased Head Circumference, Vici Syndrome, and Centronuclear Myopathy.

Dr. Keegan is a physician-scientist boarded in Medical Genetics. She completed her Medical Genetics training at University of Michigan in 2001 and has been a faculty member in the Department of Pediatrics since 2002. She currently serves as Director of the Division of Genetics, Metabolism, and Genomic Medicine in the Department of Pediatrics. She has served as the Program Director for the Medical Genetics and Genomics Residency Program since 2017. She is Co-Director of the Michigan Medicine NORD Center of Excellence and Medical Director of the Michigan Medical Genetics Laboratory. As a practicing Pediatric Medical Geneticist, she cares for patients with a wide variety of known or suspected genetic disorders and has an interest in undiagnosed rare genetic diseases. She has significant clinical expertise in genetic evaluation of patients with Differences of Sex Development (DSDs). She also participates in a multidisciplinary clinic for patients with Turner syndrome.In her spare time, she likes to travel and spend time at her cottage in Northern Michigan. Dr. Keegan is highly rated in 3 conditions, according to our data. Her clinical expertise encompasses Intersex, Aarskog Syndrome, Turner Syndrome, and Hydrocephalus due to Congenital Stenosis of Aqueduct of Sylvius.

Sara Elrefai is a Medical Genetics provider practicing medicine in Charlotte, North Carolina. Dr. Elrefai is highly rated in 3 conditions, according to our data. Her clinical expertise encompasses HER2 Negative Breast Cancer, Li-Fraumeni Syndrome, BRCA Positive Breast Cancer, and Hypothalamic Hamartomas. Dr. Elrefai is board certified in American Board Of Medical Genetics.

Dr. Paul Hillman earned his medical degree at Texas A&M College of Medicine. He completed his internship in pediatrics and his residency in pediatrics and medical genetics at McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth). In practice since 2015, Dr. Hillman is board certified in both pediatrics and medical genetics. His primary clinical interests are medical genetics, inborn errors of metabolism, lysosomal storage disorders, imprinting disorders and epigenetics. He treats patients of all ages. Dr Hillman makes certain that his patients understand the process of genetic testing and dedicates as much time as necessary to answer questions about their diagnoses. His patients value the time and effort he spends to secure genetic testing and to fully explain the meaning of the results after testing is complete. He is a fellow of the American College of Medical Genetics and an assistant professor of pediatrics at McGovern Medical School. Dr. Hillman is a resident of Houston. Dr. Hillman is highly rated in 3 conditions, according to our data. His clinical expertise encompasses Smith-Lemli-Opitz Syndrome, Angelman Syndrome, Microcephaly, and Tetrasomy 9p.