New Grant!!

We received our first R01 from NIDCR to study the causes of Van der Woude syndrome, the most common syndromic form of orofacial clefts. In the next 5 years, we hope to identify the genes that when mutated cause VWS in the 25% of VWS families that currently have no known cause. We also hope to identify genetic modifiers that explain the highly variable phenotypes within VWS families.

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Craniofacial genetics: where are we going?

We teamed up with colleagues Seth Weinberg (University of Pittsburgh) and Rob Cornell (University of Iowa) to curate a special craniofacial genetics collection for PLOS Genetics. We selected published papers in PLOS journals reflecting our particular areas of interest: craniofacial morphogenesis, dysmorphology and syndromes, and normal human facial variation. We highlighted papers that made substantial contributions to the craniofacial field and looked to the future in high-throughput functional studies, phenotyping, and genomics.

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We're presenting at ACPA!

We'll be at the 75th Annual American Cleft Palate-Craniofacial Association meeting in Pittsburgh, PA. Elizabeth will be presenting a talk, "A Systematic Analysis Of Orofacial Clefts Reveals Subtype-Specific Genetic Effects" at the Genetics Concurrent Session on Friday, April 13 at 11am. It looks to be a great session with a focus on a the genetic risk factors for subtle and not-so-subtle craniofacial phenotypes.

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