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Nature Communications|December 23, 2015
NSD1 mutations generate a genome-wide DNA methylation signatureS Choufani, C Cytrynbaum, B H Y Chung, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2024
Integrated clinical risk prediction of type 2 diabetes with a multifactorial polygenic risk scoreScott C Ritchie, Henry J Taylor, Yujian Liang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2026
KMT2A and KMT2B episignatures address diagnostic challenges associated with rare neurodevelopmental disordersZain Awamleh, Anthony Chen, Sanaa Choufani, et al.
The Journal of Antibiotics|February 5, 2015
A new antibiotic with potent activity targets MscLIrene Iscla, Robin Wray, Paul Blount, et al.
Cancer Research|March 14, 2018
Activation of the Receptor Tyrosine Kinase AXL Regulates the Immune Microenvironment in GlioblastomaHirokazu Sadahiro, Kyung-Don Kang, Justin T Gibson, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|August 2, 2017
Laying Waste to Mercury: Inexpensive Sorbents Made from Sulfur and Recycled Cooking OilsMax J H Worthington, Renata L Kucera, Inês S Albuquerque, et al.
Journal of the American Chemical Society|December 3, 2025
Making and Unmaking Poly(trisulfides) with Light: Precise Regulation of Radical Concentrations via Pulsed LED IrradiationThomas P Nicholls, Jasmine M M Pople, Madison R Harvey, et al.
BMC Genomics|November 18, 2009
Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridizationJm Friedman, Shelin Adam, Laura Arbour, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 19, 2019
Rare SUZ12 variants commonly cause an overgrowth phenotypeSharri S Cyrus, Ana S A Cohen, Ruky Agbahovbe, et al.
Medrxiv : the Preprint Server for Health Sciences|May 9, 2025
Identifying Rare Germline Variants Associated with Metastatic Prostate Cancer Through an Extreme Phenotype StudyYen-Yi Lin, Hamideh Sharifi Noghabi, Stanislav Volik, et al.
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