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Science Advances|July 2, 2025
In situ evidence for serpentinization within the Máaz formation, Jezero crater, MarsNicholas J Tosca, Michael M Tice, Joel A Hurowitz, et al.
Frontiers in Public Health|November 29, 2023
Corrigendum: <i>LetsTalkShots</i>: personalized vaccine risk communicationDaniel A Salmon, Matthew Z Dudley, Janesse Brewer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 30, 2019
De novo and biallelic DEAF1 variants cause a phenotypic spectrumMaria J Nabais Sá, Philip J Jensik, Stacey R McGee, et al.
Nature Communications|November 21, 2024
GPATCH11 variants cause mis-splicing and early-onset retinal dystrophy with neurological impairmentAndrea Zanetti, Gwendal Dujardin, Lucas Fares-Taie, et al.
Experimental Dermatology|October 15, 2020
What causes hidradenitis suppurativa ?-15 years afterChristos C Zouboulis, Farida Benhadou, Angel S Byrd, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 27, 2020
The broad phenotypic spectrum of PPP2R1A-related neurodevelopmental disorders correlates with the degree of biochemical dysfunctionLisa Lenaerts, Sara Reynhout, Iris Verbinnen, et al.
JAMA Dermatology|September 27, 2023
Outcome Measures for the Evaluation of Treatment Response in Hidradenitis Suppurativa for Clinical Practice: A HiSTORIC Consensus StatementNicole Mastacouris, Rachel Tannenbaum, Andrew Strunk, et al.
JAMA Dermatology|November 26, 2025
Standardization of Lesion Classification and Assessment by Investigators in Clinical Trials for Hidradenitis Suppurativa: A Consensus Exercise Using a Modified Delphi ApproachAmit Garg, Andrew Strunk, Bria Midgette, et al.
Kidney International|December 28, 2023
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
American Journal of Human Genetics|May 21, 2024
Etiological involvement of KCND1 variants in an X-linked neurodevelopmental disorder with variable expressivityTassja Kalm, Claudia Schob, Hanna Völler, et al.
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