25 of the Best Geneticists Near Me

Kari Casas, MD, is a specialist in pediatric and metabolic genetics. Dr. Casas is highly rated in 3 conditions, according to our data. Her clinical expertise encompasses Ornithine Transcarbamylase Deficiency, Ornithine Translocase Deficiency, Phenylketonuria (PKU), and Increased Head Circumference. Dr. Casas is board certified in American Board Of Medical Genetics: Clinical Genetics Br> American Board Of Medical Genetics: Clinical Biochemical Genetics.

Jesse Thoene is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Thoene is highly rated in 2 conditions, according to our data. His clinical expertise encompasses Argininosuccinic Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Glycine Encephalopathy, and Inborn Amino Acid Metabolism Disorder. Dr. Thoene is board certified in Clinical Biochemical Genetics and Pediatrics.

Dr. David Valle is a professor of pediatrics and ophthalmology at the Johns Hopkins School of Medicine and former director of the Johns Hopkins Department of Genetic Medicine. He also serves as a geneticist for the Johns Hopkins Children’s Center. Dr. Valle holds a bachelor’s degree and medical degree from Duke University. He completed a pediatric residency at Johns Hopkins University before joining the Johns Hopkins faculty. He is interested in the genetic contributions to health and disease. He is the founding director of the Johns Hopkins Center for Inherited Disease Research. Over the years, his laboratory has discovered the genetic causation for more than 20 diseases, including those responsible for inborn errors of metabolism, inherited retinal degeneration, disorders of cellular organelle biogenesis and genetic variations that contribute risk for common disorders such as schizophrenia. Dr. Valle also serves as director of the Predoctoral Training Program in Human Genetics, as well as co-director of the Genes to Society program. He was a 2014 recipient of the annual Victor A. McKusick Leadership Award from the American Society of Human Genetics, which recognizes individuals whose professional achievements have fostered and enriched the development of human genetics as well as its assimilation into the broader context of science, medicine and health. Dr. Valle is highly rated in 2 conditions, according to our data. His clinical expertise encompasses Spondyloepimetaphyseal Dysplasia Strudwick Type, Micrognathia, Urea Cycle Disorders (UCD), and Spondyloepiphyseal Dysplasia Congenita. Dr. Valle is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

Willa Thorson is a Medical Genetics provider practicing medicine in Miami, Florida. Dr. Thorson is highly rated in 2 conditions, according to our data. Her clinical expertise encompasses CHARGE Syndrome, Classic Galactosemia, KBG Syndrome, and Galactosemia. Dr. Thorson is currently accepting new patients.

Craig Baker is a Medical Genetics provider practicing medicine in Omaha, Nebraska. He has been practicing medicine for over 11 years. Dr. Baker is highly rated in 2 conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Propionic Acidemia, Methylmalonic Acidemia, and Adrenoleukodystrophy (ALD).

Kumarie Latchman is a Medical Genetics provider practicing medicine in Boca Raton, Florida. Dr. Latchman is highly rated in 2 conditions, according to our data. Her clinical expertise encompasses Classic Galactosemia, Early Infantile Epileptic Encephalopathy, Choanal Atresia, and Galactokinase Deficiency. Dr. Latchman is currently accepting new patients.

Joseph Tucker is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Farmington, Connecticut. He has been practicing medicine for over 21 years. Dr. Tucker is highly rated in 1 condition, according to our data. His clinical expertise encompasses Phenylketonuria (PKU) and Klinefelter Syndrome. Dr. Tucker is board certified in American Board Of Medical Genetics And Genomics, Clinical Genetics And Genomics (MD), Clinical Genetics And Genomics and American Board Of Pediatrics. Dr. Tucker is currently accepting new patients.

Shira Ziegler is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Baltimore, Maryland. Dr. Ziegler is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Hypercementosis, Inborn Amino Acid Metabolism Disorder, Homocystinuria, and Maple Syrup Urine Disease. Dr. Ziegler is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

Changqing Xia is a Medical Genetics provider practicing medicine in Omaha, Nebraska. He has been practicing medicine for over 27 years. Dr. Xia is highly rated in 1 condition, according to our data. His clinical expertise encompasses Chromosome 13q Deletion and Wolf-Hirschhorn Syndrome.

Marta Waberski is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Fairfax, Virginia. Dr. Waberski is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Perlman Syndrome, Fabry Disease, Multiple Sulfatase Deficiency, and Megalencephalic Leukoencephalopathy with Subcortical Cysts.

Andrew Feinberg studied mathematics and humanities at Yale in the Directed Studies honors program, and he received his B.A. (1973) and M.D. (1976) from the accelerated medical program at Johns Hopkins University, as well as an M.P.H. from Johns Hopkins (1981). He performed a postdoctoral fellowship in developmental biology at UCSD, clinical training in medicine at University of Pennsylvania, and genetics research and clinical training at Johns Hopkins. Dr. Feinberg is considered the founder of the field of cancer epigenetics, having discovered altered DNA methylation in cancer in the early 1980’s with Bert Vogelstein. Over the decades since, Feinberg and his colleagues have shaped the landscape of our understanding of DNA methylation and other epigenetic changes, and their applications to epidemiology and medicine, and have introduced groundbreaking statistical and laboratory methods to the study of the epigenome. He and his colleagues discovered human imprinted genes and loss of imprinting (LOI) in cancer, and they proved the epigenetic hypothesis of cancer through their work on Beckwith-Wiedemann syndrome. Most recently, they pioneered genome-scale epigenetics (epigenomics), with the first NIH funded Epigenome Center, pioneering methods including the first comprehensive genome-scale methylation discovering the major target for epigenetic variation in humans, CpG island shores. He led the first whole genome bisulfite sequencing analysis of human cancer, discovering large hypomethylated blocks that correspond to nuclear lamina-associated heterochromatin, as well as a mechanism for disruption of these blocks in epithelial-mesenchymal transition. He has also helped to create the field of epigenetic epidemiology, discovering epigenetic mediation of genetic variants in disease. He has made several important theoretical contributions as well, including the epigenetic progenitor hypothesis of cancer and the role of entropy in epigenetic development and disease. He is a Bloomberg Distinguished Professor in the Johns Hopkins University Schools of Medicine, Engineering and Public Health, where he is Director of the Center for Epigenetics. He is a recipient of an NIH Director’s Pioneer Award, is a member of the National Institute of Medicine, the American Academy of Arts and Science, the NIH Council of Councils, and he has received honorary doctorates from the University of Uppsala, the Karolinska Institute, and the University of Amsterdam. Feinberg Lab Website. Dr. Feinberg is highly rated in 1 condition, according to our data. His clinical expertise encompasses Autism Spectrum Disorder, Acute Myeloid Leukemia (AML), Leukemia, and Metabolic Syndrome. Dr. Feinberg is board certified in American Board Of Medical Genetics And Genomics and American Board Of Internal Medicine.

Dr. Rachel Li specializes in clinical and pediatric genetics. Dr. Li is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Early Infantile Epileptic Encephalopathy, Periventricular Heterotopia, Focal or Multifocal Malformations in Neuronal Migration, and Phenylketonuria (PKU). Dr. Li is board certified in American Board Of Medical Genetics And GenomicsAmerican Board Of Pediatrics.

D. Isum Ward, MD,provides a variety of services in medical genetics. He commonly treats metabolic disease and offers personalized care to those with rare conditions. Dr. Ward is highly rated in 1 condition, according to our data. His clinical expertise encompasses Glutaric Acidemia Type 2, Temple Syndrome, Tetrasomy 9p, and Chromosome 11 Uniparental Disomy. Dr. Ward is board certified in American Board Of PediatricsAmerican Board Of Medical Genetics.

Joel Gabre is a Medical Genetics specialist and a Gastroenterologist practicing medicine in New York, New York. Dr. Gabre is highly rated in 1 condition, according to our data. His clinical expertise encompasses Barrett Esophagus, Esophageal Cancer, DICER1 Syndrome, and Colorectal Cancer. Dr. Gabre is board certified in Internal Medicine. Dr. Gabre is currently accepting new patients.

Amna Othman is a Medical Genetics provider practicing medicine in Ann Arbor, Michigan. Dr. Othman is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Rhizomelic Syndrome, Pfeiffer Syndrome, and Williams Syndrome.

Nicholas Borja is a Medical Genetics provider practicing medicine in Miami, Florida. Dr. Borja is highly rated in 1 condition, according to our data. His clinical expertise encompasses KBG Syndrome, Sotos Syndrome, Coffin-Siris Syndrome, and Mosaicism. Dr. Borja is currently accepting new patients.

Dr. Falah is a Medical Doctor specializing in Medical Genetics and Metabolic Disorders. She is a former assistant professor in the Department of Pediatrics, Division of Genetics and Metabolism, at West Virginia University. Additionally, she previously served on the West Virginia Advisory Council on Rare Diseases, with a particular focus on rare diseases.Dr. Falah earned her medical degree from Tripoli University of Medical Science in Tripoli, Libya. She then completed a residency in clinical genetics at the University of Miami Leonard M. Miller School of Medicine/Jackson Health System. Following this, Dr. Falah pursued a fellowship in clinical pharmacology at the Indiana University School of Medicine/IU Health. She also holds a Master of Science degree in Clinical Investigation from Vanderbilt University in Nashville, Tennessee. To further advance her expertise in genetics, she completed a medical biochemical fellowship at Duke University.Dr. Falah is board-certified in Medical Genetics and Medical Biochemical Genetics by the American Board of Medical Genetics and Genomics (ABMGG). She has been a member of the American College of Medical Genetics and Genomics and the American Medical Association since 2014. Dr. Falah’s work has been published in peer-reviewed journals, and she has presented at various medical conferences. She also serves as a reviewer for several medical journals and as a consultant for private pharmaceutical companies. Dr. Falah is highly rated in 1 condition, according to our data. Her clinical expertise encompasses 46XX Testicular Disorder of Sex Development, Waardenburg Syndrome Type 1, Pelizaeus-Merzbacher Disease, and Waardenburg Syndrome. Dr. Falah is board certified in American Board Of Medical Genetics.

As the Medical Director for the Adult Genetics Clinic at BCM I am proud to say that this is one of the largest Adult Genetics Clinic in the country. My primary clinical focus lies in diagnosis and management of adults with genetic conditions, known or suspected. These include diagnosis and management of single gene disorders, chromosomal disorders and familial cancer syndromes; risk assessment for cancer and reproductive planning as well as testing for known genetic disorders in the family. I have developed a keen interest and a valuable expertise in management of connective tissue disorders such as Ehlers Danlos syndrome as patients from far and near come to me for evaluation. I am also involved in education of medical students at BCM particularly in the field of adult genetics. I am one of the track directors for the Genetics track, the first such medical school track of its kind in the country, where students get an unparalleled experience in genetics over and above what they learn in their core courses. My research focus is on diagnosing rare genetic disorders and I am the team leader for adult genetics for the Undiagnosed Disease Network Project currently ongoing at BCM in collaboration with several other centers across the nation. Dr. Dhar is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Ehlers-Danlos Syndrome (EDS), Autism Spectrum Disorder, Clouston Syndrome, and Ectodermal Dysplasias.

Marie Beall is a Neonatologist and a Medical Genetics provider practicing medicine in Van Nuys, California. Her clinical expertise encompasses Gestational Diabetes, Premature Infant, Placenta Previa, and ABO Incompatibility. Dr. Beall is board certified in Medical Genetics And Genomics Clin Genetics & Genomic, OB & Gyn (Sub: Maternal And Fetal Medicine), and Obstetrics & Gynecology. Dr. Beall is currently accepting new patients.

John Thorson is a Medical Genetics provider practicing medicine in San Diego, California. His clinical expertise encompasses Retinopathy Pigmentary Mental Retardation, Myeloproliferative Neoplasms (MPN), Chromosome 13q Duplication, and Trisomy 13.

Candace Gamble is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Fort Worth, Texas. Her clinical expertise encompasses Hypotonia, Achondroplasia, Smith-Magenis Syndrome, and Miller-Dieker Syndrome.

Roger Klein is a Medical Genetics provider practicing medicine in Portsmouth, Ohio. His clinical expertise encompasses Fasciotomy and Reconstructive Urology Surgery.

Sandesh Sreenath Nagamani, MD, is dedicated to delivering high-quality, compassionate care to Houston and nearby communities. Sandesh Sreenath Nagamani specializes in Clinical Genetics and Genomics and works at BCM-Adult Genetics. To make an appointment, please call (713) 798-7820. To review all accepted insurance carriers, please visit: https://www.stlukeshealth.org/patients-visitors/patients/billing-insurance/insurances-accepted. His clinical expertise encompasses Osteogenesis Imperfecta and Neurofibromatosis Type 1 (NF1). Dr. Nagamani is currently accepting new patients.

Miguel Rivera is a Medical Genetics provider practicing medicine in Boston, Massachusetts. His clinical expertise encompasses ALK-Positive Non-Small Cell Lung Cancer.

Alexandra Flores is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Fort Worth, Texas. Her clinical expertise encompasses Hypotonia, Mixed Gonadal Dysgenesis, Turner Syndrome, and Chromosome 13q Deletion.