ºÚÁÏÍø

Skip to main content

Shawn Ahmed’s group reports on a novel mechanism of gene silencing in Caenorhabditis elegans, termed “multigenerational RNAe”

September 14, 2015
The title of the article, published in PNAS, is “Lack of pairing during meiosis triggers multigenerational transgene silencing in Caenorhabditis elegans.” Co-first authors are Luciana Leopold, a graduate student in the Curriculum in Genetics and Molecular Biology, and Bree Heestand, a postdoctoral fellow in Shawn’s lab. This silencing process can...

Genetics and Medicine faculty team up for a study of microRNAs in Crohn’s disease

July 27, 2015
Bailey Peck, a Genetics and Molecular Biology graduate student in Praveen Sethupathy’s lab, is first author of a collaborative paper, with Bioinformatics and Computational Biology grad student Matthew Weiser (Furey lab), Shehzad Sheikh, Assistant Professor of Medicine and Genetics (senior author), and Drs. Sethupathy and Furey as coauthors. The article...

Jim Evans prominent in national discussions on Genomic Medicine

February 20, 2015
Jim was one of four discussants on NPR’s “On Point” and coauthor of an editorial in JAMA The “On Point” discussion, related to President Obama’s announcement regarding the Precision Medicine Initiative, is available as a podcast. In the JAMA Viewpoint article, Jim and Michael Watson of the ACMG Foundation for...

Sara Selitsky has first-authored a paper published in Scientific Reports (Nature’s open access journal).

January 16, 2015
The title of the paper is “Small tRNA-derived RNAs are increased and more abundant than microRNAs in chronic hepatitis B and C.” Sara is a BCB graduate student who is co-mentored by Praveen Sethupathy and Stan Lemon (Department of Medicine). In this study, Selitsky et al. identify for the first...

Article by Terry Furey’s group highlighted in Genetics

November 11, 2014
Matt Weiser, a graduate student in Terry’s lab, is first author on the paper, entitled “Novel Distal eQTL Analysis Demonstrates Effect of Population Genetic Architecture on Detecting and Interpreting Associations.” Standard eQTL mapping methods carry significant multiple testing burdens, limiting their ability to detect eQTL distal to the affected gene....

Shawn Ahmed and colleagues publish a paper in PNAS demonstrating a novel function of two C. elegans RNA interference proteins

October 27, 2014
Shawn and Eric Miska at the University of Cambridge are senior authors on the paper, and Shawn’s former postdoc, Aisa Sakaguchi, and former graduate student, Matt Simon, as co-first authors with Peter Sarkies from Dr. Miska’s lab. This study establishes a role for small RNAs in promoting transgenerational fertility via...

Fernando Pardo-Manuel de Villena has been elected to the Board of Directors of the Genetics Society of America (GSA).

September 22, 2014
Fernando will serve a three-year term beginning January 1, 2015. See the official announcement on the GSA web site. The GSA is the professional membership organization for scientific researchers and educators in the field of genetics, with over 5,000 members. Society members work to advance knowledge in the basic mechanisms...

Three Department of Genetics faculty members are ranked as most cited in their fields

July 2, 2014
Yun Li, Karen Mohlke, and Chuck Perou are among the top 1% most cited world researchers in their subject fields for 2014. Thomson Reuters has listed Yun and Karen among the most highly cited in Molecular Biology & Genetics and Chuck in Clinical Medicine. To see the complete list and...

Jim Evans and Chuck Perou are featured in a Special Section on Breast Cancer in Science

April 14, 2014
Evans and Perou are quoted regarding the risks of reporting germline mutations in numerous genes implicated in rare forms of hereditary predispositions to breast cancer. Chuck points out that there are probably 10 – 100 genes in addition to BRCA1 and BRCA2 that may contribute to breast cancer susceptibility. Both...

Terry Furey and Praveen Sethupathy coauthor a Perspective in Science

November 15, 2013
The article discusses three reports on DNA variants in the human genome that affect gene regulation epigenetically, via sequence-specific binding-affinity of transcription factors.