Gregory Cooper, Ph.D.
Affiliations: | Genome Sciences | University of Washington, Seattle, Seattle, WA |
Google:
"Gregory Cooper"
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. |
| Hiatt SM, Lawlor JM, Handley LH, et al. (2024) Long-read genome sequencing and variant reanalysis increase diagnostic yield in neurodevelopmental disorders. Medrxiv : the Preprint Server For Health Sciences |
| Rahman MA, Cai C, Bo N, et al. (2023) An individualized Bayesian method for estimating genomic variants of hypertension. Bmc Genomics. 23: 863 |
| Moyers BA, Loupe JM, Felker SA, et al. (2023) Allele biased transcription factor binding across human brain regions gives mechanistic insight into eQTLs. Biorxiv : the Preprint Server For Biology |
| Felker SA, Lawlor JM, Hiatt SM, et al. (2023) Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testing. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100884 |
| Felker SA, Lawlor JM, Hiatt SM, et al. (2023) Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testing. Biorxiv : the Preprint Server For Biology |
| Hiatt SM, Trajkova S, Sebastiano MR, et al. (2022) Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype. American Journal of Human Genetics |
| Bowling KM, Thompson ML, Kelly MA, et al. (2022) Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing. Genome Medicine. 14: 131 |
| Hiatt SM, Lawlor JMJ, Handley LH, et al. (2021) Long-read genome sequencing for the molecular diagnosis of neurodevelopmental disorders. Hgg Advances. 2 |
| Scott TM, Guo H, Eichler EE, et al. (2020) BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability and autism spectrum disorder. Human Mutation |
| Carapito R, Ivanova EL, Morlon A, et al. (2019) ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder. American Journal of Human Genetics |