Donna M. Werling, B.S.
Affiliations: | University of California, Los Angeles, Los Angeles, CA |
Area:
Neurogenetics, AutismGoogle:
"Donna Werling"Mean distance: 16.45 (cluster 6) | S | N | B | C | P |
Parents
Sign in to add mentorDaniel Geschwind | grad student | 2009-2014 | UCLA | |
(Investigation of sex-differential genetic risk factors for autism spectrum disorders.) | ||||
Stephan J. Sanders | post-doc | UCSF | ||
Matthew W. State | post-doc |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Liang L, Fazel Darbandi S, Pochareddy S, et al. (2021) Developmental dynamics of voltage-gated sodium channel isoform expression in the human and mouse brain. Genome Medicine. 13: 135 |
Kissel LT, Werling DM. (2020) Neural Transcriptomic Analysis of Sex Differences in Autism Spectrum Disorder: Current Insights and Future Directions. Biological Psychiatry |
Werling DM, Pochareddy S, Choi J, et al. (2020) Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex. Cell Reports. 31: 107489 |
Werling DM. (2019) Clinically Defined Subtypes of Bipolar Disorder Are Reflected in Genomic Architecture. Biological Psychiatry. 86: 78-80 |
Werling D, Pochareddy S, Choi J, et al. (2019) 29 BRAINVAR DATA SET: WHOLE-GENOME AND RNA SEQUENCING REVEAL VARIATION AND TRANSCRIPTOMIC COORDINATION IN THE DEVELOPING HUMAN PREFRONTAL CORTEX European Neuropsychopharmacology. 29: S75-S76 |
An J, Lin K, Zhu L, et al. (2019) INSIGHTS INTO THE CONTRIBUTION OF RARE NONCODING VARIATION IN AUTISM SPECTRUM DISORDER THROUGH FAMILY-BASED WHOLE-GENOME SEQUENCING European Neuropsychopharmacology. 29: S36 |
Werling D, Brand H, An J, et al. (2019) LIMITED CONTRIBUTION OF RARE, NONCODING VARIATION TO AUTISM SPECTRUM DISORDER FROM SEQUENCING OF 2,076 GENOMES IN QUARTET FAMILIES European Neuropsychopharmacology. 29: S784-S785 |
Li M, Santpere G, Imamura Kawasawa Y, et al. (2018) Integrative functional genomic analysis of human brain development and neuropsychiatric risks. Science (New York, N.Y.). 362 |
An JY, Lin K, Zhu L, et al. (2018) Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder. Science (New York, N.Y.). 362 |
Werling DM, Brand H, An JY, et al. (2018) An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. Nature Genetics |