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Sherif Gerges
@SherifMorris
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Coptic PhD Student @harvard working on single-cell genetics/omics with Mark Daly & Steve McCarroll. @broadinstitute | @harvardmed | @MGH_RI | 🇪🇬🇺🇸
Boston, MA
Joined April 2011
RT @andrewwhite01: We’ve just finished writing the missing 15,616 Wikipedia articles to get complete coverage of all 19,255 human genes. We…
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@kulesatony Oh very cool! Added to my list of resources for looking up functions of genes. Perhaps this will complement OMIM or even supersede it...
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RT @ElliotHershberg: Hub-and-Spoke Biotechs: Nimbus Therapeutics I wrote about how Nimbus's fundamental business model innovation enabled…
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RT @kulesatony: After today's Nobel, there couldn't be a better day to announce this 📢 Together with ARIA, we are building a new fellowshi…
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RT @MushtaqBilalPhD: Academics paid $1.06 billion (with a B) to five academic publishers from 2015-2018 in publication fees. Publishers' R…
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@ChidiAkusobi felt like my IQ dropped a standard deviation. bloviating hubris and cluelessness masquerading as some insightful analysis
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@SashaGusevPosts Huh very intriguing, BMI is definitely well powered to study this but intrigued as to how this can explain overlap of psychiatric disorders e.g SCZ and BD (can't think of a proper meditator tho).
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Woah, pretty stunning finding. A stretch of 18 bp in a non-coding gene, RNU4-2, linked to a non-trivial percentage of NDD cases. Also interesting is that the de novo variants were all on the maternal allele. Very cool!
So excited that our paper “De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome” is out today in @Nature 🧵 1/16
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