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Reymundo Lozano, MD, Medical Genetics, New York, NY

ReymundoLozanoMD

Medical Genetics • New York, NY

Clinical Genetics, Ph.D. Medical Genetics, Pediatric Medical Genetics

Assistant Professor

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Education & Training

  • Universidad de Guadalajara
    Universidad de GuadalajaraClass of 2005

Certifications & Licensure

  • CA State Medical License
    CA State Medical License 2010 - Present
  • NY State Medical License
    NY State Medical License 2015 - 2025
  • American Board of Pediatrics Pediatrics
  • American Board of Medical Genetics and Genomics Clinical Genetics and Genomics

Awards, Honors, & Recognition

  • Early career Achievement Award Universidad de Guadalajara, 2014
  • The winner, Annual Resident’s week New York University, 2008
  • 2nd Prize, Best Poster of Research Brooklyn Pediatric Society, 2008
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Clinical Trials

Publications & Presentations

PubMed

Journal Articles

  • New FOXP1 mutation causes autism and severe hypotonia  
    Lozano R, Lozano C, Deroziti P, Human Mutation, 1/20/2015
  • Methadone use in a male with the fmr1 premutation and FXTAS  
    Muzar Z, Lozano R, Schneider A, Adams P., Faradz S, Tassone F, Hagerman R, AJMG, 1/10/2015
  • A novel ZRS mutation leads to preaxial polydactyly type 2 in a heterozygous form and Werner Mesomelic syndrome in a homozygous form  
    VanderMeer J., Lozano R., Sun M., Xue Y., Wang Jabs E., Wilcox W., Ahituv N., Hum Mutat, 1/28/2014
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Books/Book Chapters

  • New Developments in Treatment for Neurodevelopmental Disorders 
    Chapter: Treatment of Fragile X syndrome and Fragile X- associated Disorders 
    Lozano R., Hare E. and Hagerman REditors: Robert L. Hendren, Randi and Hagerman.
  • Health Care for people with Intellectual and Developmental Disabilities across the lifespan 
    Chapter: Fragile X syndrome 
    Hare E., Lozano R, Partington L and Hagerman REditors: Rubin and Crocker.Edition 3rd,
  • Molecular and genetic Basis of Neurological and Psychiatric Disease 
    Chapter: Genetic Basis of Psychiatric Diseases 
    Lozano R. Hare E. and Hagerman REdition 5th,

Abstracts/Posters

  • Macroorchidism in Premutation Carriers
    Lozano R, International National Foundation for Fragile X syndrome, 1/1/2014
  • Gabaergic Treatments for children with FXS
    Lozano R, International National Foundation for Fragile X syndrome, 1/1/2014
  • FMR1 Base Second Hit Model in Premutation Carriers
    Lozano R, American Society of Human Genetics, 1/1/2014
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Lectures

  • Outreach engagement “Colombia project of Hope” 
    1/24/2015
  • Genetic Diagnosis and treatments for Autism 
    1/12/2015
  • Gabaergic treatments for FXS 
    1/24/2014
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Other

  • University Radio/ Fragile X syndrome and Autism 
    Lozano R, University of Guadalajara
    1/1/2015
  • Clinical, genetic and psychological considerations of neurological disorders: focus on intellectual disability 
    Lozano R, PCHD19 Alliance and Ambry Genetics, Autism awareness month webinar
    1/8/2014
  • Clinic work-flow in the clinics at the MIND institute 
    Lozano R, MIND Institute, UC Davis advertisement
    1/1/2014
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Press Mentions

  • Daily Checkup: Down Syndrome Is Most Common Chromosomal Condition; Increased Risk of Other Health Issues
    Daily Checkup: Down Syndrome Is Most Common Chromosomal Condition; Increased Risk of Other Health IssuesNovember 22nd, 2015

Dr. Reymundo Lozano, Dr. Reymundo Lozano, MD, Dr. R Lozano