Mohammad A. Faghihi

Medical Genetics
9000 SW 152nd St Ste 209
Palmetto Bay, FL 33157

Last Updated: 09/26/2026

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Found 53 publications

Analysis of a deeply-phenotyped familial hypercholesterolemia cohort from Mexico shows a role for both rare and common alleles across known dyslipidemia genes and reveals structural variation in a novel locus.

Analysis of a deeply-phenotyped familial hypercholesterolemia cohort from Mexico shows a role for both rare and common alleles across known dyslipidemia genes and reveals structural variation in a novel locus.

Journal: Human genomics
Published: July 31, 2025

Identification of Candidate Genes for Pigmentation in Camels Using Genotyping-by-Sequencing.

Identification of Candidate Genes for Pigmentation in Camels Using Genotyping-by-Sequencing.

Journal: Animals : an open access journal from MDPI
Published: February 18, 2022

Genetic Testing in Various Neurodevelopmental Disorders Which Manifest as Cerebral Palsy: A Case Study From Iran.

Genetic Testing in Various Neurodevelopmental Disorders Which Manifest as Cerebral Palsy: A Case Study From Iran.

Journal: Frontiers in pediatrics
Published: July 01, 2021

A novel knockout mouse model of the noncoding antisense Brain-Derived Neurotrophic Factor (Bdnf) gene displays increased endogenous Bdnf protein and improved memory function following exercise.

A novel knockout mouse model of the noncoding antisense Brain-Derived Neurotrophic Factor (Bdnf) gene displays increased endogenous Bdnf protein and improved memory function following exercise.

Journal: Heliyon
Published: April 20, 2021

Generalized exfoliative skin rash as an early predictor of supratherapeutic voriconazole trough levels in a leukemic child: A case report.

Generalized exfoliative skin rash as an early predictor of supratherapeutic voriconazole trough levels in a leukemic child: A case report.

Journal: Current medical mycology
Published: April 09, 2021

High-throughput imaging of ATG9A distribution as a diagnostic functional assay for adaptor protein complex 4-associated hereditary spastic paraplegia.

High-throughput imaging of ATG9A distribution as a diagnostic functional assay for adaptor protein complex 4-associated hereditary spastic paraplegia.

Journal: Brain communications
Published: April 07, 2021

Molecular diagnostic assays for COVID-19: an overview.

Molecular diagnostic assays for COVID-19: an overview.

Journal: Critical reviews in clinical laboratory sciences
Published: February 17, 2021

Genomic prediction for growth using a low-density SNP panel in dromedary camels.

Genomic prediction for growth using a low-density SNP panel in dromedary camels.

Journal: Scientific reports
Published: November 15, 2020

Role of IgG against N-protein of SARS-CoV2 in COVID19 clinical outcomes.

Role of IgG against N-protein of SARS-CoV2 in COVID19 clinical outcomes.

Journal: Scientific reports
Published: September 29, 2020

A Neurite Outgrowth Assay and Neurotoxicity Assessment with Human Neural Progenitor Cell-Derived Neurons.

A Neurite Outgrowth Assay and Neurotoxicity Assessment with Human Neural Progenitor Cell-Derived Neurons.

Journal: Journal of visualized experiments : JoVE
Published: August 25, 2020

Potential voriconazole associated posterior reversible leukoencephalopathy in children with malignancies: Report of two cases.

Potential voriconazole associated posterior reversible leukoencephalopathy in children with malignancies: Report of two cases.

Journal: Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
Published: July 22, 2020

Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.

Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.

Journal: Frontiers in genetics
Published: July 19, 2020
Showing 1-12 of 53

Last Updated: 09/26/2026