This issue of the SFARI newsletter includes: (1) 2017 SFARI Pilot and Research, Explorer and Bridge to Independence Awards announced, (2) Simons Simplex Collection, (3) Simons VIP, (4) SPARK, (5) SFARI Gene, (6) SFARI channel on BioRxiv, (7) SFARI.org relaunch, (8) SFARI funding, (9) SFARI-funded publications, (10) Simons Foundation Autism Research lecture series.
This issue of the SFARI newsletter includes: (1) SFARI 2017 Explorer awardees announced, (2) SFARI 2017 Bridge to Independence Award finalists announced, (3) A Conversation with SFARI investigator David Ginty, (4) SFARI Explorer Awards - Request for Applications, (5) SFARI-Funded publications, (6) Past lecture: Daniel Geschwind, “Autism genetics: Searching for coherence”.
This issue of the SFARI newsletter includes: (1) SFARI 2017 Pilot and Research awardees announced, (2) SFARI Gene: New data release, (3) Whole-exome sequencing of SPARK: New data release, (4) SFARI Social at Neuroscience 2017, (5) Presentations by SFARI Investigators at Neuroscience 2017, (6) 2018 Pilot and Research Awards -— Request for Applications, (7) Highlights of SFARI-Funded Research, (8) Upcoming lecture: Daniel Geschwind, “Autism genetics: Searching for coherence”, (9) Past lecture: Paola Arlotta, “Understanding autism and other neurodevelopmental disorders: From the embryo to brain organoids”, (10) Past lecture: David Ledbetter, “Leveraging long-term health data and exome sequencing for autism-related gene discovery”.
This issue of the SFARI newsletter includes: (1) 2018 Pilot and Research Awards - Request for Applications, (2) Whole-genome sequencing of the Simons Simplex Collection: New data release, (3) Simons Variation in Individuals Project (Simons VIP): New data release, (4) Newly redesigned SFARI website, (5) Newly redesigned SFARI Gene website, (6) SFARI's 2018 funding priorities, (7) 2018 Pilot and Research Award applications: The review process, (8) A Conversation with Sharmila Banerjee-Basu about SFARI Gene, (9) Upcoming lecture: David Ledbetter, “Leveraging long-term health data and exome sequencing for autism-related gene discovery”.