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Reymundo Lozano

University of California, Davis
Icahn School of Medicine at Mount Sinai

45

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684

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The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder.

2021 Human Mutation
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Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptoms.

2021 Molecular Autism
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Identity and Reproductive Aspects in Females with Fragile X Syndrome

2021
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Strong evidence for genotype-phenotype correlations in Phelan-McDermid syndrome: Results from the developmental Synaptopathies consortium.

2021 Human Molecular Genetics
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Prospective and detailed behavioral phenotyping in DDX3X syndrome

2021 medRxiv
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Focused Revision: ACMG practice resource: Genetic evaluation of short stature.

2021 Genetics in Medicine
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SURAMIN INTRAVENOUS INFUSION FOR TREATING BOYS WITH AUTISM SPECTRUM DISORDER: RESULTS OF A 14-WEEK, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTIDOSE, PHASE 2 STUDY

2021 Journal of the American Academy of Child and Adolescent Psychiatry
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Prospective and detailed behavioral phenotyping in DDX3X syndrome.

2021 Molecular Autism
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FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring.

2021 Journal of Neurodevelopmental Disorders
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Response to Placebo in Fragile X Syndrome Clinical Trials: An Initial Analysis.

2020 Brain Sciences
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