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  1. Article

    Open Access

    Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82

    Alopecia areata is a complex genetic disease that results in hair loss due to the autoimmune-mediated attack of the hair follicle. We previously defined a role for both rare and common variants in our earlier ...

    Stephanie O. Erjavec, Sahar Gelfman, Alexa R. Abdelaziz in Nature Communications (2022)

  2. Article

    Open Access

    Publisher Correction: TCF7L2 polymorphisms are associated with amygdalar volume in elderly individuals with Type 2 Diabetes

    An amendment to this paper has been published and can be accessed via a link at the top of the paper.

    Ithamar Ganmore, Abigail Livny, Ramit Ravona-Springer, Itzik Cooper in Scientific Reports (2020)

  3. Article

    Open Access

    TCF7L2 polymorphisms are associated with amygdalar volume in elderly individuals with Type 2 Diabetes

    The association between several Single Nucleotide Polymorphisms (SNPs) within the transcription factor 7-like 2 (TCF7L2) gene and Type 2 Diabetes (T2D) as well as additional T2D-related traits is well established...

    Ithamar Ganmore, Abigail Livny, Ramit Ravona-Springer, Itzik Cooper in Scientific Reports (2019)

  4. No Access

    Article

    Noncoding deletions reveal a gene that is critical for intestinal function

    Large-scale genome sequencing is poised to provide a substantial increase in the rate of discovery of disease-associated mutations, but the functional interpretation of such mutations remains challenging. Here...

    Danit Oz-Levi, Tsviya Olender, Ifat Bar-Joseph, Yiwen Zhu, Dina Marek-Yagel in Nature (2019)