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European Journal of Human Genetics : EJHG|March 20, 2025
Heterozygous CELF4 variants in the N-term region crucial for the RNA-binding activity lead to neurodevelopmental disorder and obesityAnge-Line Bruel, Anneke T Vulto-vanSilfhout, Frédéric Bilan, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|May 20, 2015
Establishing a Nomogram for Stage IA-IIB Cervical Cancer Patients after Complete ResectionHang Zhou, Xiong Li, Yuan Zhang, et al.
Medrxiv : the Preprint Server for Health Sciences|November 22, 2024
Loss of DOT1L disrupts neuronal transcription, behavior, and leads to a neurodevelopmental disorderMarissa J Maroni, Melissa Barton, Katherine Lynch, et al.
Brain : a Journal of Neurology|June 10, 2025
Loss of DOT1L disrupts neuronal transcription and leads to a neurodevelopmental disorderMarissa J Maroni, Melissa Barton, Katherine Lynch, et al.
Brain : a Journal of Neurology|September 15, 2023
TRAPPC6B biallelic variants cause a neurodevelopmental disorder with TRAPP II and trafficking disruptionsHashem Almousa, Sara A Lewis, Somayeh Bakhtiari, et al.
American Journal of Human Genetics|December 25, 2024
Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disabilityPascale Sabeh, Samantha A Dumas, Claudia Maios, et al.
Nature Genetics|July 3, 2013
A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12Yongyong Shi, Li Li, Zhibin Hu, et al.
Journal of Affective Disorders|February 20, 2021
Disrupted hemispheric connectivity specialization in patients with major depressive disorder: Evidence from the REST-meta-MDD ProjectYu-Dan Ding, Ru Yang, Chao-Gan Yan, et al.
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