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- Specialties
- View section
- Allergology
- Angiology and Vascular Surgery
- Digestive System
- Cardiology
- Interventional Cardiology
- Pediatric Cardiology
- Cardiovascular Surgery
- General Surgery
- Oral and Maxillofacial Surgery
- Plastic and Aesthetic Surgery
- Thoracic Surgery
- Oncological Support Team
- Advanced Dermatology
- Endocrinology
- Medical Physics
- Physical Therapy and Rehabilitation
- Medical Genetics
- Gynecology and Obstetrics
- Hematology and Hemotherapy
- Immunology
- Clinical Analysis Laboratory
- Intensive Care Medicine
- Internal Medicine
- Nuclear Medicine
- Clinical Microbiology
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- Neurosurgery
- Neurology
- Dentistry
- Ophthalmology
- Medical Oncology
- Radiation Oncology
- Otorhinolaryngology
- Pediatrics, Adolescence, and Young Adults
- Radiological Protection
- Psychiatry
- Gamma Radiosurgery and Functional Neurosurgery
- Radiodiagnosis
- Rheumatology
- Traumatology
- Sports Traumatology
- Assisted Reproduction
- Urology
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Juan Bernar Solano
Especialista en Genética Médica. Formado en la Universidad de California en Los Ángeles (UCLA) . Experto en metabolopatías, retraso del neurodesarrollo y métodos diagnósticos.
Jefe de Equipo de Unidad de Genética Médica- Hospital Ruber Internacional
Especialista en Genética Médica. Formado en la Universidad de California en Los Angeles (UCLA) y "fellow" en los Institutos Nacionales de la Salud de Bethesda, Maryland especializándose en metabolopatías, retraso del neurodesarrollo y métodos diagnósticos.
En 1991, y tras la estancia en EE.UU, establece el laboratorio de Genética Médica del Hospital Ruber Internacional realizando citogenética clásica y molecular aplicada al diagnóstico prenatal principalmente. También citogenética molecular (FISH) aplicada a determinados tipos de tumores. Desde el punto de vista clínico, valoración de pacientes con retraso mental, epilepsia y malformaciones congénitas. Consejo genético a pacientes y familias con enfermedades hereditarias.
1991-actualidad|Laboratorio de Genética Médica del Hospital Ruber Internacional.
1984|American Board Medical Genetics, EE.UU.
1980|Licenciado en Medicina y cirugía, por la Universidad Complutense de Madrid.
- Valoración y diagnóstico de pacientes con retraso mental:
- Malformaciones congénitas:
2023|Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia. Enviado para publicación.
2018| Specificity of electroclinical features in the diagnosis of ring chromosome 20. Epilepsy and behaviour. 2018 mar; 80, 215–220.
2016|Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie Syndrome. PLoS One 2016 Apr 28;11(4):e0153757.
2009|Familial cerebral cavernous malformations associated with a splice site CCM2 deletion. J Neurol. 2009 Jan;256(1):137-8.
2008|Multiple motor system dysfunction associated with a heterozygous ceruloplasmin gene mutation. J Neurol. 2008 Jul;255(7):1083-4.
Sociedades científicas a las que pertenece:
-American College of Medical Genetics.
-American Society of Human genetics.