Photo of Paul Psychogios, MD

Paul Psychogios, MD

Accepting New Patients
181 South Buena Vista Street, Suite 110
Burbank, CA 91505
2273.9 miles away
Medical Groups & Affiliations
Providence Specialty Medical Group
Speaks: French, Greek and English
map

Providence Clinical Genetics and Genomics Program - Burbank

181 South Buena Vista Street, Suite 110, Burbank, CA 91505

Are you covered?

Check to see if your insurance is covered by this provider.

About Paul Psychogios

Dr. Apostolos “Paul” Psychogios is a board-certified medical geneticist. He completed his graduate medical studies and cardiology training at the University of Athens in Greece, medical and clinical genetics at Columbia University, and clinical molecular genetics at Harvard Medical School. Before joining Providence, Dr. Paul worked at Mayo Clinic, Cleveland Clinic, and Vanderbilt University amongst other centers. He founded the first cardiovascular genetics service at the University of Kentucky. His practice focuses on hereditary cancer, cardiovascular disorders, renal disorders, pharmacogenomics, precision medicine, and unknown etiology disorders.

Residency

Columbia University Medical Center
2005

Medical School

University of Athens
1989

Fellowship

Harvard Medical School
2006

Internship

Northeastern Ohio University
2003

Board Certifications
  • American Board of Medical Genetics and Genomics, Clinical Genetics (MD)
  • American Board of Genetics and Genomics, Clinical Genetics
Providence Clinical Genetics and Genomics Program - Burbank
181 South Buena Vista Street, Suite 110
Burbank, CA 91505

Providence Clinical Genetics and Genomics Program - Saint John's
2200 Santa Monica Boulevard
Santa Monica, CA 90404

Medical Groups & Affiliations
Providence Specialty Medical Group

Affiliated Locations
Saint John’s Health Center Cancer Clinic – Santa Monica
Providence Saint Joseph Medical Center
Providence St. Joseph Hospital - Orange

Clinical Interests

  • Abdominal Wall Defect
  • Achondroplasia
  • Acrocephalosyndactyly
  • Adrenoleukodystrophy (Ald)
  • Aicardi Syndrome
  • Alagille Syndrome
  • Albinism
  • Alpha 1 Antitrypsin Deficiency
  • Alport Syndrome
  • Anal Stenosis
  • Androgen Insensitivity
  • Angelman Syndrome
  • Aniridia
  • Apc Gene
  • Arteriovenous Malformation (Avm)
  • Autism
  • Axin2 Gene
  • Bap1 Gene
  • Bard1 Gene
  • Barth Syndrome
  • Becker Muscular Dystrophy
  • Beckwith Wiedemann Syndrome
  • Blepharophimosis
  • Blood Disorders
  • Blue Diaper Syndrome
  • Bmpr1a Gene
  • Bohring Opitz Syndrome (Bos)
  • Bone Disorders
  • Brca
  • Breast Cancer Genetic Testing
  • Breast Cancer Genetics
  • Brugada Syndrome
  • C Syndrome
  • Cafe Au Lait Spots
  • Cancer Predisposition Syndromes
  • Cardiac Genetics
  • Cardiomyopathy
  • Carnitine Deficiency
  • Cataract
  • Cdh13 Gene
  • Cdk4 Gene
  • Cdkl5 Mutation
  • Cdkn2a Gene
  • Cerebellar Anomalies
  • Cerebral Anomalies
  • Cerebral Palsy
  • Charcot Marie Tooth Disease
  • Charge Syndrome
  • Checkpoint Kinase 2
  • Childhood Obesity
  • Chromosomal Microarray Analysis
  • Chromosome Abnormality
  • Chronic Granulomatous Disorder
  • Cirrhosis
  • Cleidocranial Dysostosis
  • Coloboma
  • Congenital Adrenal Hyperplasia
  • Congenital Diaphragmatic Hernia (Cdh)
  • Congenital Esophageal Atresia
  • Congenital Generalized Lipodystrophy
  • Congenital Heart Disease
  • Congenital Hyperinsulinism
  • Congenital Limb Defects
  • Connective Tissue Disorder
  • Cornelia De Lange Syndrome
  • Costello Syndrome
  • Cutis Aplasia
  • Cyp2c19 Mutation
  • Cyp2d6 Mutation
  • Cystic Fibrosis
  • Cystic Fibrosis Gene Carrier
  • Deafness
  • Denys Drash Syndrome (Dds)
  • Developmental Delay
  • Developmental Regression
  • Diabetes Mellitus
  • Diaphragmatic Hernia
  • Dicer1 Gene
  • Digeorge Syndrome
  • Disorders Of Sexual Differentiation
  • Down Syndrome
  • Duane Syndrome
  • Duchenne Muscular Dystrophy
  • Dup15q Syndrome
  • Dystonia
  • Ectodermal Dysplasias
  • Edema
  • Ehlers Danlos
  • Ellis-Van Creveld Syndrome
  • Epcam Gene
  • Epilepsy
  • Esophageal Atresia
  • Exercise Intolerance
  • Facial Asymmetry
  • Facioscapulohumeral Muscular Dystrophy
  • Failure To Thrive
  • Familial Medullary Thyroid Cancer (Fmtc)
  • Familial Partial Lipodystrophy
  • Familial Spinal Muscle Atrophy
  • Family History Of Birth Defects
  • Family History Of Cancer
  • Family History Of Colon Cancer
  • Family History Of Colon Polyps
  • Family History Of Glaucoma
  • Fatal Familial Insomnia (Ffi)
  • Fetal Alcohol Syndrome
  • Fetal Growth Restriction
  • Fish Cancer Test
  • Flcn Gene
  • Fracture
  • Fragile X Syndrome
  • Frasier Syndrome
  • Galnt12 Gene
  • Gaucher Disease
  • Genetic Counseling
  • Genetic Disorders
  • Genetic Dystonia
  • Genetic Testing Colon Cancer
  • Genetic Testing Ovarian Cancer
  • Glaucoma
  • Glaucoma Of Childhood
  • Glucose Galactose Malabsorption (Ggm)
  • Glycogen Storage Disease
  • Gorlin Syndrome
  • Grem1 Gene
  • Grin Mutation
  • Hearing Loss
  • Hearing Loss (Genetic)
  • Hemihypertrophy
  • Hemochromatosis
  • Hemoglobinopathies
  • Hemophagocytic Lymphohistiocytosis
  • Hemophilia
  • Hemophilia Inhibitors
  • Her2 Positive Breast Cancer
  • Hereditary Hemorrhagic Telangiectasia
  • Hereditary Polyposis
  • Hereditary Retinoblastoma
  • Hereditary Spastic Paraplegia
  • Hermansky Pudlak Syndrome
  • Hirschsprung's Disease
  • Holt-Oram Syndrome
  • Hormone Receptor Positive Breast Cancer
  • Hoxb13 Gene
  • Hunter Syndrome
  • Hurler Syndrome
  • Hydrocephalus
  • Hypermobility Syndrome
  • Hypertrophic Cardiomyopathy
  • Hypoglycemia
  • Hypophosphatasia
  • Hypospadias
  • Hypotonia
  • Immune Deficiency
  • Inborn Errors Of Metabolism
  • Infertility
  • Intellectual Disabilities
  • Intestinal Atresia
  • Ipex Syndrome
  • Kabuki Syndrome
  • Kcnb1 Mutation
  • Kearns Sayre Syndrome
  • Kidney Dysplasia
  • Kit Gene
  • Klinefelter Syndrome
  • Klippel Trenaunay Syndrome
  • Learning Disabilities
  • Learning Disorders
  • Leigh's Disease
  • Leukodystrophy
  • Li Fraumeni Syndrome
  • Lissencephaly
  • Long Qt Syndrome
  • Lynch Syndrome
  • Lysosomal Diseases
  • Macrocephaly
  • Marfan Syndrome
  • Maroteaux Lamy Syndrome
  • Maturity Onset Diabetes Of The Young
  • Max Gene
  • Mckusick-Kaufman Syndrome (Mkks)
  • Met Gene
  • Met Proto-Oncogene Receptor Tyrosine Kinase Mutation
  • Metabolic Acidosis
  • Metabolic Disorders (Inherited)
  • Microcephaly
  • Micrognathia
  • Microphthalmos
  • Mitf Gene
  • Mitochondrial Disorders