Mental Health Repository

JOURNAL PROFILE

Gene

Publications (565)

Education in Twins and Their Parents Across Birth Cohorts Over 100 years: An Individual-Level Pooled Analysis of 42-Twin Cohorts

Journal: Twin Res Hum Genet

Publication Year: 2017

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Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference

Journal: Nat Genet

Publication Year: 2024

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Genome-wide analysis of a model-derived binge eating disorder phenotype identifies risk loci and implicates iron metabolism

Journal: Nat Genet

Publication Year: 2023

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A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program

Journal: PLoS Genet

Publication Year: 2022

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PGAP3-related hyperphosphatasia with mental retardation syndrome: Report of 10 new patients and a homozygous founder mutation

Journal: Clin Genet

Publication Year: 2018

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Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability

Journal: Am J Hum Genet

Publication Year: 2014

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Influence of COVID-19 pandemic lockdown on a sample of Egyptian children with Down syndrome

Journal: Egypt J Med Hum Genet

Publication Year: 2022

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Analysis of selected polymorphisms in FOXP3 gene in a cohort of Egyptian patients with schizophrenia

Journal: J Genet Eng Biotechnol

Publication Year: 2022

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Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features

Journal: Am J Hum Genet

Publication Year: 2016

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Pathogenic variants in PIDD1 lead to an autosomal recessive neurodevelopmental disorder with pachygyria and psychiatric features

Journal: Eur J Hum Genet

Publication Year: 2021

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An integrated multiomic approach as an excellent tool for the diagnosis of metabolic diseases: our first 3720 patients

Journal: Eur J Hum Genet

Publication Year: 2022

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Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome

Journal: Am J Hum Genet

Publication Year: 2020

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Bi-allelic GOT2 Mutations Cause a Treatable Malate-Aspartate Shuttle-Related Encephalopathy

Journal: Am J Hum Genet

Publication Year: 2019

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The Challenges and Opportunities for Mental Health Twin Research in Nigeria

Journal: Behav Genet

Publication Year: 2024

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Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16-20 October 2015

Journal: Psychiatr Genet

Publication Year: 2016

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Family History of Twinning and Fertility Traits in Nigerian Mothers of Dizygotic Twins

Journal: Twin Res Hum Genet

Publication Year: 2024

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Bidirectional Causal Associations Between Same-Sex Attraction and Psychological Distress: Testing Moderation and Mediation Effects

Journal: Behav Genet

Publication Year: 2023

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Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry

Journal: Am J Hum Genet

Publication Year: 2021

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Genotype-phenotype feasibility studies on khat abuse, traumatic experiences and psychosis in Ethiopia

Journal: Psychiatr Genet

Publication Year: 2020

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The oligogenic model of amyotrophic lateral sclerosis; phenotypes of three Tunisian families

Journal: Clin Genet

Publication Year: 2022

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Phylogenetic and amino acid signature analysis of the SARS-CoV-2s lineages circulating in Tunisia

Journal: Infect Genet Evol

Publication Year: 2022

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Expanding the phenotype of TARDBP mutation in a Tunisian family with clinical phenotype heterogeneity

Journal: Amyotroph Lateral Scler Frontotemporal Degener

Publication Year: 2022

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CDC14A phosphatase is essential for hearing and male fertility in mouse and human

Journal: Hum Mol Genet

Publication Year: 2018

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Optineurin in patients with Amyotrophic Lateral Sclerosis associated to atypical Parkinsonism in Tunisian population

Journal: Amyotroph Lateral Scler Frontotemporal Degener

Publication Year: 2024

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A novel frame shift mutation in the PQBP1 gene identified in a Tunisian family with X-linked mental retardation

Journal: Eur J Med Genet

Publication Year: 2011

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Prenatal diagnosis of chromosome disorders in Tunisian population

Journal: Ann Genet

Publication Year: 2001

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Comorbidity of bathing suit ichthyosis and limb-girdle muscular dystrophy type 2 A in a Tunisian patient revealed by Whole Exome Sequencing

Journal: Gene

Publication Year: 2024

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New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families

Journal: Neurogenetics

Publication Year: 2004

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A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum

Journal: Neurogenetics

Publication Year: 2010

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Explanatory models for the cause of Fragile X Syndrome in rural Cameroon

Journal: J Genet Couns

Publication Year: 2021

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Cascade Testing for Fragile X Syndrome in a Rural Setting in Cameroon (Sub-Saharan Africa)

Journal: Genes (Basel)

Publication Year: 2020

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Association between serotonin transporter gene polymorphisms and increased suicidal risk among HIV positive patients in Uganda

Journal: BMC Genet

Publication Year: 2017

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Internalizing Mental Disorders and Accelerated Cellular Aging Among Perinatally HIV-Infected Youth in Uganda

Journal: Front Genet

Publication Year: 2019

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Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Journal: Am J Hum Genet

Publication Year: 2016

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Cytogenetic analysis of 5572 patients referred for suspected chromosomal abnormalities in Morocco

Journal: Genet Test Mol Biomarkers

Publication Year: 2012

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Mowat-Wilson syndrome in a Moroccan consanguineous family

Journal: Indian J Hum Genet

Publication Year: 2007

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A recurrent mutation in Moroccan patients with Dyggve-Melchior-Clausen syndrome: Report of a new case and review

Journal: Indian J Hum Genet

Publication Year: 2011

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The prolactin receptor (PRLR) gene is linked to and associated with the comorbidity of depression and type 2 diabetes in Italian families

Journal: Genes Dis

Publication Year: 2023

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The role of melatonin receptor 1B gene (MTNR1B) in the susceptibility to depression and type 2 diabetes comorbidity

Journal: Genes Dis

Publication Year: 2023

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Objective evaluation of facial features in Congolese newborns by facial measurements. The need for population-specific measurements

Journal: Am J Med Genet A

Publication Year: 2022

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