| Keeping an eye on Bardet-Biedl syndrome: a comprehensive review of the role of Bardet-Biedl syndrome genes in the eye K Weihbrecht, WA Goar, T Pak, JE Garrison, AP DeLuca, EM Stone, ... Medical research archives 5 (9), 2017 | 93 | 2017 |
| Genotypic and phenotypic characterization of the Sdccag8Tn(sb-Tyr)2161B.CA1C2Ove mouse model K Weihbrecht, WA Goar, CS Carter, VC Sheffield, S Seo PLoS One 13 (2), e0192755, 2018 | 11 | 2018 |
| Exome-based investigation of the genetic basis of human pigmentary glaucoma C van der Heide, W Goar, KJ Meyer, WLM Alward, EA Boese, NC Sears, ... BMC genomics 22 (1), 477, 2021 | 8 | 2021 |
| Development and application of a computable genotype model in the GA4GH Variation Representation Specification W Goar, L Babb, S Chamala, M Cline, RR Freimuth, RK Hart, K Kuzma, ... PACIFIC SYMPOSIUM ON BIOCOMPUTING 2023: Kohala Coast, Hawaii, USA, 3–7 …, 2022 | 3 | 2022 |
| Targeted mutation of nuclear bone morphogenetic protein 2 impairs secondary immune response in a mouse model DS Olsen, WA Goar, BA Nichols, KT Bailey, SL Christensen, KR Merriam, ... BioMed research international 2015, 2015 | 3 | 2015 |
| A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigree MJ Schnieders, WA Goar, M Griess, BR Roos, TE Scheetz, EM Stone, ... Eye, 2018 | 2 | 2018 |
| Computational strategies to investigate the genetic cause of human eye disease WA Goar The University of Iowa, 2019 | 1 | 2019 |
| 36. Gene Normalizer: A tool to resolve genetic ambiguity through data harmonization A Smith, J Stevenson, K Kuzma, W Goar, M Cannon, A Wagner Cancer Genetics 278, 11, 2023 | | 2023 |
| 58. Implementing the ClinGen/CGC/VICC oncogenicity guidelines in a pediatric variant classification workflow W Goar, K Kuzma, K Stahl, K Voytovich, M Mathew, E Macke, M Babcock, ... Cancer Genetics 278, 18, 2023 | | 2023 |
| P654: Evaluation of the ClinGen/CGC/VICC Oncogenicity Guidelines to support pediatric variant classification workflows W Goar, K Kuzma, K Stahl, K Voytovich, M Mathew, E Macke, M Babcock, ... Genetics in Medicine Open 1 (1), 2023 | | 2023 |
| EXOME-BASED INVESTIGATION OF THE GENETIC BASIS OF PIGMENT DISPERSION SYNDROME W Goar, C van der Heide, B Roos, WLM Alward, YH Kwon, M Anderson, ... Investigative Ophthalmology & Visual Science 60 (9), 2836-2836, 2019 | | 2019 |
| Exome sequencing analysis in three Bedouin families with Keratoconus W Goar, P Majdalani, CC Searby, SS Whitmore, AP DeLuca, A Imtirat, ... Investigative Ophthalmology & Visual Science 58 (8), 3556-3556, 2017 | | 2017 |
| Examination of sequencing data in three Israeli families with Keratoconus WA Goar, CC Searby, SS Whitmore, AP DeLuca, A Imtirat, EM Stone, ... Investigative Ophthalmology & Visual Science 57 (12), 4823-4823, 2016 | | 2016 |
| Nuclear localized BMP2 promotes cell cycle progression BA Nichols, WA Goar, BT McCune, LC Bridgewater The FASEB Journal 27, 1029.1-1029.1, 2013 | | 2013 |
| Advancing the AI/ML-Readiness of gnomAD Data with GA4GH Genomic Knowledge Standards A Wagner, W Goar, K Ferriter, D Marten, K Laricchia, K Chao, L Babb | | |
| Research Article Targeted Mutation of Nuclear Bone Morphogenetic Protein 2 Impairs Secondary Immune Response in a Mouse Model DS Olsen, WA Goar, BA Nichols, KT Bailey, SL Christensen, KR Merriam, ... | | |
| Targeted mutation of nuclear bone morphogenetic protein 2 (nBMP2) impairs secondary immune response in a mouse model DS Olsen, WA Goar, BA Nichols, KT Bailey, S Loyd, KR Christensen, ... | | |
