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Nature Genetics|August 9, 2018
Author Correction: Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body compositionKerrin S Small, Marijana Todorčević, Mete Civelek, et al.
Nature Genetics|April 11, 2018
Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body compositionKerrin S Small, Marijana Todorčević, Mete Civelek, et al.
The CRISPR Journal|October 23, 2020
Reactions to the National Academies/Royal Society Report on Heritable Human Genome EditingMisha Angrist, Rodolphe Barrangou, Françoise Baylis, et al.
American Journal of Medical Genetics. Part A|February 8, 2023
A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall statureAlanna Strong, Soumya Rao, Sandra von Hardenberg, et al.
Circulation. Cardiovascular Genetics|April 20, 2010
Candidate gene association resource (CARe): design, methods, and proof of conceptKiran Musunuru, Guillaume Lettre, Taylor Young, et al.
Nature|May 20, 2021
In vivo CRISPR base editing of PCSK9 durably lowers cholesterol in primatesKiran Musunuru, Alexandra C Chadwick, Taiji Mizoguchi, et al.
The New England Journal of Medicine|May 15, 2025
Patient-Specific In Vivo Gene Editing to Treat a Rare Genetic DiseaseKiran Musunuru, Sarah A Grandinette, Xiao Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2023
De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset strokeTheresa Brunet, Benedikt Zott, Victoria Lieftüchter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 16, 2026
New genotype-phenotype correlations and management recommendations for individuals with RERE variantsDavid Curtis, Xiaonan Zhao, Nichole M Owen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Stankiewicz-Isidor syndrome: expanding the clinical and molecular phenotypeBertrand Isidor, Frédéric Ebstein, Anna Hurst, et al.
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