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T Humphreys

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Circulation. Genomic and Precision Medicine|May 18, 2022

Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome SequencingIngrid Tarr, Stephanie Hesselson, Siiri E Iismaa, et al.

Nature Genetics|December 24, 2025

Designing synthetic regulatory elements using the generative AI framework DNA-DiffusionLucas Ferreira DaSilva, Simon Senan, Judith F Kribelbauer-Swietek, et al.

Human Molecular Genetics|December 4, 2020

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and miceElla M M A Martin, Annabelle Enriquez, Duncan B Sparrow, et al.

The New England Journal of Medicine|August 10, 2017

NAD Deficiency, Congenital Malformations, and Niacin SupplementationHongjun Shi, Annabelle Enriquez, Melissa Rapadas, et al.

Pageof 14

Search research articles

Showing results (131-140 of 134) with videos related to

Sort By:

Pageof 14

You have reached the last page of results.This site can display upto 134 results.

Circulation. Genomic and Precision Medicine|May 18, 2022

Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome SequencingIngrid Tarr, Stephanie Hesselson, Siiri E Iismaa, et al.

Nature Genetics|December 24, 2025

Designing synthetic regulatory elements using the generative AI framework DNA-DiffusionLucas Ferreira DaSilva, Simon Senan, Judith F Kribelbauer-Swietek, et al.

Human Molecular Genetics|December 4, 2020

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and miceElla M M A Martin, Annabelle Enriquez, Duncan B Sparrow, et al.

The New England Journal of Medicine|August 10, 2017

NAD Deficiency, Congenital Malformations, and Niacin SupplementationHongjun Shi, Annabelle Enriquez, Melissa Rapadas, et al.

Pageof 14