about
Evaluation and identification of damaged single nucleotide polymorphisms in COL1A1 gene involved in osteoporosis.Computational Analysis of Breast Cancer GWAS Loci Identifies the Putative Deleterious Effect of STXBP4 and ZNF404 Gene Variants.MED12 is recurrently mutated in Middle Eastern colorectal cancer.Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus.Mutation in MPDZ causes severe congenital hydrocephalus.Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.Molecular modelling and dynamics of CA2 missense mutations causative to carbonic anhydrase 2 deficiency syndromeWhole-Exome Sequencing of Matched Primary and Metastatic Papillary Thyroid CancerEvolution and Impact of Subclonal Mutations in Papillary Thyroid CancerPrognostic significance of DNMT3A alterations in Middle Eastern papillary thyroid carcinomaTGFβ-induced SMAD4-dependent Apoptosis Proceeded by EMT in CRCPrevalence, spectrum, and founder effect of BRCA1 and BRCA2 mutations in epithelial ovarian cancer from the Middle EastStructural prediction, whole exome sequencing and molecular dynamics simulation confirms p.G118D somatic mutation of PIK3CA as functionally important in breast cancer patients
P50
Q37321850-D6D21289-B782-4384-AFB4-A498C10A7C15Q38830789-2AE00744-9391-4560-9A89-5CA6CBCC0950Q38968909-13A99907-A1FB-40C8-BEAA-A54711104BC3Q45342398-274D88D5-9B78-44EF-B01B-57D06D0E29A5Q47830125-CE98DAD7-7EE3-4345-AB33-A6DC5B1EE7CEQ53640716-034F4957-8D2F-47DB-95B8-B4CC1467F8D2Q90203753-5E3D8B87-7D38-45FC-A8DC-17AF4488328BQ91021310-BAE687D2-92C1-45F9-AE8D-692A2C636896Q91024032-893FDB71-0B60-4FBB-80E3-EA483FF7B2EEQ91678942-7A91AAD3-1E9B-43BB-9B6C-66292B837B7DQ91750472-622364DB-B7D7-4600-8592-5DD490917676Q92067332-F7BC9A7A-0AE6-4164-8BB2-E250B697CF80Q92588084-12739BE5-BC7E-47A6-B83B-8096D60CDD74
P50
description
investigador
@es
researcher
@en
name
Tariq Ahmad Masoodi
@en
type
label
Tariq Ahmad Masoodi
@en
prefLabel
Tariq Ahmad Masoodi
@en
P108
P31
P496
0000-0002-9186-6349