Geneticist Search Results
Richard Chang is a Medical Genetics provider practicing medicine in Orange, California. Dr. Chang is highly rated in 156 conditions, according to our data. His clinical expertise encompasses Phenylketonuria (PKU), Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Maternal Hyperphenylalaninemia, and Adrenoleukodystrophy (ALD). Dr. Chang is currently accepting new patients.
City Of Hope's Helford Clinical Research Hospital
Raju Pillai is a Medical Genetics provider practicing medicine in Duarte, California. Dr. Pillai is highly rated in 7 conditions, according to our data. His clinical expertise encompasses Smoldering Multiple Myeloma, Relapsed Refractory Multiple Myeloma (RRMM), T-Cell Lymphoma, Myeloproliferative Neoplasms (MPN), and Liver Embolization.
Lpch Medical Group Div Of Lucile
David Stevenson is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Palo Alto, California. Dr. Stevenson is highly rated in 100 conditions, according to our data. His clinical expertise encompasses Neurofibromatosis Type 1 (NF1), Neurofibromatosis, RASopathies, Costello Syndrome, and Deep Brain Stimulation.
UC Irvine Medical Center
Dr. Virginia E. Kimonis is a board-certified UCI Health clinician-scientist who specializes in the diagnosis and treatment of children and adults with neuromuscular, neurodegenerative, dysmorphia and other complex disorders.Her clinical interests include inclusion body myopathy, Paget disease, Pompe disease, frontotemporal dementia, Prader Willi syndrome, morbid obesity and craniosynostosis.Kimonis earned her medical degree at the University of Southampton Medical School in Southampton, England. She completed a residency in pediatrics at Massachusetts General Hospital in Boston, followed by a fellowship in clinical and biochemical genetics at the National Institutes of Health (NIH) and Children's National Hospital in Washington, D.C.The author or co-author of more than 175 peer-reviewed publications in prestigious journals, Kimonis has focused her research primarily on inherited muscle disorders, lysosomal storage diseases, Prader Willi and several other rare disorders. She developed the Lysosomal Disease Program, established a registry study among a large cohort of patients with Pompe disease, and conducted a study of resistance training for axial and respiratory muscles in Pompe disease as an adjunct to enzyme replacement treatment.She also discovered multisystem proteinopathy, a new disease type associated with mutations in the VCP gene that overlaps with Pompe disease. She has received research funding from numerous agencies, including NIH, the Muscular Dystrophy Association, the Paget Foundation and other rare disease foundations.Kimonis also is a lead investigator with the newly establishedNational Organization for Rare Disorders (NORD) Rare Disease Center of Excellence, a joint program of UCI Health and Children's Hospital of Orange County (CHOC). Dr. Kimonis is highly rated in 17 conditions, according to our data. Her clinical expertise encompasses Prader-Willi Syndrome, Pompe Disease, Fabry Disease, Danon Disease, and Hormone Replacement Therapy (HRT). Dr. Kimonis is board certified in American Board Of Medical Genetics And Genomics - Clinical Genetics And Genomics.
City Of Hope Medical Foundation
Stephen Gruber is a Medical Genetics specialist and an Oncologist practicing medicine in Duarte, California. Dr. Gruber is highly rated in 10 conditions, according to our data. His clinical expertise encompasses Colorectal Cancer, Familial Colorectal Cancer, Lynch Syndrome, Melanoma, and Colonoscopy.
Lpch Medical Group Div Of Lucile
Gregory Enns is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Palo Alto, California. Dr. Enns is highly rated in 54 conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Methylmalonic Acidemia, Arginase Deficiency, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Dr. Enns is currently accepting new patients.
Raymond Wang is a Medical Genetics provider practicing medicine in Orange, California. Dr. Wang is highly rated in 47 conditions, according to our data. His clinical expertise encompasses Mucopolysaccharidosis Type 4A (MPS IVA, Morquio Syndrome Type A), Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome), Mucopolysaccharidoses (MPS), and Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Dr. Wang is currently accepting new patients.
Jose Abdenur is a Medical Genetics provider practicing medicine in Orange, California. Dr. Abdenur is highly rated in 42 conditions, according to our data. His clinical expertise encompasses Von Gierke Disease, Glycogen Storage Disease Type 9, Glycogen Storage Disease Type 3, and Malonyl-CoA Decarboxylase Deficiency. Dr. Abdenur is currently accepting new patients.
Lpch Medical Group Div Of Lucile
Dena Matalon is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Palo Alto, California. Dr. Matalon is highly rated in 137 conditions, according to our data. Her clinical expertise encompasses Campomelia Cumming Type, Microcephaly, Microcephaly Deafness Syndrome, and Coffin-Lowry Syndrome.
Lpch Medical Group Div Of Lucile
Christina Tise is a Medical Genetics provider practicing medicine in Palo Alto, California. Dr. Tise is highly rated in 133 conditions, according to our data. Her clinical expertise encompasses Zellweger Syndrome, 2q37 Deletion Syndrome, Urea Cycle Disorders (UCD), and Adrenoleukodystrophy (ALD).
Rady Children's Hospital San Diego
Lynne Bird is a Medical Genetics specialist and a Pediatrics provider practicing medicine in San Diego, California. Dr. Bird is highly rated in 32 conditions, according to our data. Her clinical expertise encompasses Angelman Syndrome, Prader-Willi Syndrome, VACTERL Association, Mucolipidosis Type 4, and Gastrostomy.
The Regents Of The University Of California
Deborah Krakow is a Medical Genetics specialist and an Obstetrics and Gynecologist practicing medicine in Los Angeles, California. Dr. Krakow is highly rated in 29 conditions, according to our data. Her clinical expertise encompasses Osteogenesis Imperfecta, Chondrodystrophy, Acromicric Dysplasia, and Acrofacial Dysostosis Catania Type.
Matthew Deardorff is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Los Angeles, California. Dr. Deardorff is highly rated in 27 conditions, according to our data. His clinical expertise encompasses Cornelia De Lange Syndrome, Coffin-Siris Syndrome, Mosaicism, and Beckwith-Wiedemann Syndrome.
UC Davis Medical Center MIND Institute
Suma Shankar is a Medical Genetics provider practicing medicine in Sacramento, California. Dr. Shankar is highly rated in 16 conditions, according to our data. Her clinical expertise encompasses Gaucher Disease Type 1, RASopathies, Costello Syndrome, and Fabry Disease. Dr. Shankar is board certified in Medical Genetics And Genomics Clin Genetics & Genomic. Dr. Shankar is currently accepting new patients.
Lpch Medical Group Div Of Lucile
Anne Niehaus is a Medical Genetics provider practicing medicine in Palo Alto, California. Dr. Niehaus is highly rated in 115 conditions, according to our data. Her clinical expertise encompasses Microcephaly, Cardiomyopathy Hypogonadism Metabolic Anomalies, WAGR Syndrome, and Atelosteogenesis Type 1.
UC Davis Medical Center MIND Institute
Madelena Martin is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Sacramento, California. Dr. Martin is highly rated in 12 conditions, according to our data. Her clinical expertise encompasses Danon Disease, Pompe Disease, Phenylketonuria (PKU), and Fabry Disease. Dr. Martin is board certified in Medical Genetics And Genomics Clin Genetics & Genomic and Medical Genetics And Genomics Clin Biochemical Genetic. Dr. Martin is currently accepting new patients.
Southern California Permanente Medical Group
Moin Vera is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Los Angeles, California. Dr. Vera is highly rated in 11 conditions, according to our data. His clinical expertise encompasses Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidoses (MPS), Triple X Syndrome, and Chromosome 10q Deletion.
Lpch Medical Group Div Of Lucile
Suha Bachir is a Medical Genetics provider practicing medicine in Palo Alto, California. Dr. Bachir is highly rated in 110 conditions, according to our data. Her clinical expertise encompasses Early Infantile Epileptic Encephalopathy, 2q37 Deletion Syndrome, Costello Syndrome, and Atelosteogenesis Type 1.
Katherine Rauen is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Sacramento, California. Dr. Rauen is highly rated in 9 conditions, according to our data. Her clinical expertise encompasses RASopathies, Costello Syndrome, Legius Syndrome, and Cardiofaciocutaneous Syndrome.
Dr. Eric J. Vilain is a board-certified UCI Health pediatrician who specializes in genetic and genomic medicine.Vilain serves as associate vice chancellor for clinical and translational research and scientific affairs for the Susan and Henry Samueli College of Health Sciences and director of the Institute for Clinical and Translational Sciences at UC Irvine.He received his medical degree at the Faculté de Médecine Paris-Descartes and a doctor of Philosophy degree in genetics from the Université Pierre-et-Marie-Curie in Paris, France. Next. he completed residencies in general pediatrics and pediatric endocrinology at the Necker-Enfants Malades Hospital, followed by a residency in pediatric medical genetics and a fellowship at clinical biochemical genetics at the David Geffen School of Medicine at UCLA, where he went on to serve as a faculty member, physician and prolific genetics researcher for two decades.Before joining the UCI School of Medicine and the College of Health Sciences, he most recently worked at the Children's National Medical Center in Washington, D.C., where he served as director of the Center for Genetic Medicine Research and was the A. James Clark Distinguished Professor of Molecular Genetics.Vilain's clinical and research emphasis has long been on differences of sex development and medical genetics.He sees patients atUCI Medical Centerin Orange. Dr. Vilain is highly rated in 5 conditions, according to our data. His clinical expertise encompasses Pyle Disease, Intersex, Beckwith-Wiedemann Syndrome, Hypospadias, and Orchiectomy. Dr. Vilain is board certified in American Board Of Medical Genetics And Genomics - Clinical Genetics And Genomics.
Valley Childrens Medical Group
David Dimmock is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Modesto, California. Dr. Dimmock is highly rated in 5 conditions, according to our data. His clinical expertise encompasses Phenylketonuria (PKU), Increased Head Circumference, Micrognathia, and Dihydropteridine Reductase Deficiency. Dr. Dimmock is currently accepting new patients.
Stephen Cederbaum is a Medical Genetics provider practicing medicine in Los Angeles, California. Dr. Cederbaum is highly rated in 4 conditions, according to our data. His clinical expertise encompasses Arginase Deficiency, Urea Cycle Disorders (UCD), Phenylketonuria (PKU), and Argininosuccinic Aciduria.
Rebecca Mardach is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Los Angeles, California. Dr. Mardach is highly rated in 4 conditions, according to our data. Her clinical expertise encompasses Gaucher Disease Type 1, Gaucher Disease, Propionic Acidemia, and Farber Lipogranulomatosis.
Sequenom Center For Molecular Medicine LLC
Nilesh Dharajiya is a Medical Genetics provider practicing medicine in San Diego, California. Dr. Dharajiya is highly rated in 3 conditions, according to our data. His clinical expertise encompasses Chromosome 13q Duplication, Trisomy 13, Trisomy 18, and Tissue Biopsy.
Seymour Packman is a Medical Genetics provider practicing medicine in San Francisco, California. Dr. Packman is highly rated in 2 conditions, according to our data. His clinical expertise encompasses Gaucher Disease Type 1, Gaucher Disease, Fabry Disease, and Acid Sphingomyelinase Deficiency (ASMD).