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Ricardo Harripaul

Showing results (1-10 of 30) with videos related to

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Cold Spring Harbor Perspectives in Medicine|March 3, 2017
The Use of Next-Generation Sequencing for Research and Diagnostics for Intellectual DisabilityRicardo Harripaul, Abdul Noor, Muhammad Ayub, et al.
American Journal of Medical Genetics. Part A|March 27, 2024
When rare meets common: Treatable genetic diseases are enriched in the general psychiatric populationVenuja Sriretnakumar, Ricardo Harripaul, James L Kennedy, et al.
Journal of Human Genetics|March 5, 2020
A novel biallelic single base insertion in WNK1 in a Pakistani family with congenital insensitivity to painStephen Pastore, Ricardo Harripaul, Matloob Azam, et al.
Human Mutation|February 13, 2018
MeCP2 AT-Hook1 mutations in patients with intellectual disability and/or schizophrenia disrupt DNA binding and chromatin compaction in vitroTaimoor I Sheikh, Ricardo Harripaul, Muhammad Ayub, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 18, 2018
Enrichment of pathogenic variants in genes associated with inborn errors of metabolism in psychiatric populationsVenuja Sriretnakumar, Ricardo Harripaul, John B Vincent, et al.
Genes|September 23, 2022
Biallelic Loss of Function Mutation in Sodium Channel Gene <i>SCN10A</i> in an Autism Spectrum Disorder Trio from PakistanAnsa Rabia, Ricardo Harripaul, Anna Mikhailov, et al.
Scientific Reports|April 22, 2024
Biallelic variants identified in 36 Pakistani families and trios with autism spectrum disorderHamid Khan, Ricardo Harripaul, Anna Mikhailov, et al.
Genes|January 21, 2022
Heterozygous <i>De Novo</i> Truncating Mutation of Nucleolin in an ASD Individual Disrupts Its Nucleolar LocalizationTaimoor I Sheikh, Ricardo Harripaul, Nasim Vasli, et al.
BMC Medical Genomics|August 28, 2021
Exome sequencing identifies novel and known mutations in families with intellectual disabilityMemoona Rasheed, Valeed Khan, Ricardo Harripaul, et al.
Psychiatry Research|May 4, 2020
Prediction of physical violence in schizophrenia with machine learning algorithmsKevin Z Wang, Ali Bani-Fatemi, Christopher Adanty, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Cold Spring Harbor Perspectives in Medicine|March 3, 2017
The Use of Next-Generation Sequencing for Research and Diagnostics for Intellectual DisabilityRicardo Harripaul, Abdul Noor, Muhammad Ayub, et al.
American Journal of Medical Genetics. Part A|March 27, 2024
When rare meets common: Treatable genetic diseases are enriched in the general psychiatric populationVenuja Sriretnakumar, Ricardo Harripaul, James L Kennedy, et al.
Journal of Human Genetics|March 5, 2020
A novel biallelic single base insertion in WNK1 in a Pakistani family with congenital insensitivity to painStephen Pastore, Ricardo Harripaul, Matloob Azam, et al.
Human Mutation|February 13, 2018
MeCP2 AT-Hook1 mutations in patients with intellectual disability and/or schizophrenia disrupt DNA binding and chromatin compaction in vitroTaimoor I Sheikh, Ricardo Harripaul, Muhammad Ayub, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 18, 2018
Enrichment of pathogenic variants in genes associated with inborn errors of metabolism in psychiatric populationsVenuja Sriretnakumar, Ricardo Harripaul, John B Vincent, et al.
Genes|September 23, 2022
Biallelic Loss of Function Mutation in Sodium Channel Gene <i>SCN10A</i> in an Autism Spectrum Disorder Trio from PakistanAnsa Rabia, Ricardo Harripaul, Anna Mikhailov, et al.
Scientific Reports|April 22, 2024
Biallelic variants identified in 36 Pakistani families and trios with autism spectrum disorderHamid Khan, Ricardo Harripaul, Anna Mikhailov, et al.
Genes|January 21, 2022
Heterozygous <i>De Novo</i> Truncating Mutation of Nucleolin in an ASD Individual Disrupts Its Nucleolar LocalizationTaimoor I Sheikh, Ricardo Harripaul, Nasim Vasli, et al.
BMC Medical Genomics|August 28, 2021
Exome sequencing identifies novel and known mutations in families with intellectual disabilityMemoona Rasheed, Valeed Khan, Ricardo Harripaul, et al.
Psychiatry Research|May 4, 2020
Prediction of physical violence in schizophrenia with machine learning algorithmsKevin Z Wang, Ali Bani-Fatemi, Christopher Adanty, et al.
Pageof 3