Genetic variation: ExAC boosts clinical variant interpretation in Human genomics: A deep dive into genetic variation. “Disease study lets gene mutations off the hook” on The AustralianĮxome Aggregation Consortium (ExAC) Editorials and other coverage “Human variation decoded” on University of Sydney News “Going Deep and Wide” on Harvard Medical School News “Exome Data From 60K-Person Cohort Yields Novel Rare Variants” on GenomeWeb “Largest Human Genetic Variation Repository Yet” on The Scientist We’re finally starting to understand when those differences matter” on STAT “Largest collection of human exome sequence data yields unprecedented tool for diagnosing rare disease” on Broad Institute Media Release website

“How Data-Wranglers Are Building the Great Library of Genetic Variation” on the Atlantic by my favorite blogger Ed Yong “The Exome Aggregation Consortium (ExAC) database: shedding light on human genetic variation” – video made by Broad Institute Communication for the General Public “Improving the Diagnosis of Neuromuscular Diseases” on AANEM News on “AAA Fellows Angela and Monkol Lek continue positive impact on rare disease research” on the Australian American Association website “Monkol Lek on his humble Blacktown beginnings to the forefront of science at Harvard” on the Daily Telegraph “The Gene Bank that Weeds out Benign Mutations” on The Australian “Interview with Daniel MacArthur and Monkol Lek” on Broad Ignite Podcast “The Muscle Detectives” on the Broad Institute Giving website

“Researcher with LGMD Aims to Bring Genetic Diagnoses to People Around the World” on Muscular Dystrophy Association website On Boston Channel 5 (ABC) News promoting Strength Science and Stories of Inspiration Charity event 2017 My Journey with Muscular Dystrophy into AcademiaĪn article in Chinese that students from Prof Hongwen Zhou’s lab wrote about my journey

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