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Genetics Research|April 15, 2021
Functional Analysis of DNMT1 SNPs (rs2228611 and rs2114724) Associated with SchizophreniaSonal Saxena, Pranay Amruth Maroju, Sumana Choudhury, et al.
Brain & Development|May 29, 2004
Etiological heterogeneity of familial periventricular heterotopia and hydrocephalusVolney L Sheen, Lina Basel-Vanagaite, Jean R Goodman, et al.
Neurology|January 13, 2012
FLNA genomic rearrangements cause periventricular nodular heterotopiaK R Clapham, T W Yu, V S Ganesh, et al.
Molecular Cell|August 18, 2023
FAM120A couples SREBP-dependent transcription and splicing of lipogenesis enzymes downstream of mTORC1Sungyun Cho, Yujin Chun, Long He, et al.
Scientific Reports|November 27, 2025
Development and validation of an integrated preclinical model mimicking cardiometabolic risk in postmenopausal female ratsP Sainath, Shakta Mani Satyam, Sanjay Bharati, et al.
Revista De Neurologia|October 22, 2002
[Juvenile myoclonic epilepsy in chromosome 6p12: clinical and genetic advances]A V Delgado-Escueta, D Bai, J Bailey, et al.
Scientific Reports|September 19, 2019
Quantification of wild-type and radiation attenuated Plasmodium falciparum sporozoite motility in human skinBéatrice M F Winkel, Clarize M de Korne, Matthias N van Oosterom, et al.
Iscience|June 13, 2024
De novo TLK1 and MDM1 mutations in a patient with a neurodevelopmental disorder and immunodeficiencyMarina Villamor-Payà, María Sanchiz-Calvo, Jordann Smak, et al.
Omics : a Journal of Integrative Biology|April 1, 2021
Proteomic Alterations Associated with Oral Cancer Patients with Tobacco Using HabitsFirdous Ahmad Bhat, Sonali V Mohan, Shankargouda Patil, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
Identification of a de novo mutation in TLK1 associated with a neurodevelopmental disorder and immunodeficiencyMarina Villamor-Payà, María Sanchiz-Calvo, Jordann Smak, et al.
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