VARPRISM: incorporating variant prioritization in tests of de novo mutation association

por Hu, Hao, Coon, Hilary, Li, Man, Yandell, Mark, Huff, Chad D.
Publicado 2016

Genetic analysis of age at onset variation in spinocerebellar ataxia type 2

por Figueroa, K.P., Coon, Hilary, Santos, Nieves, Velazquez, Luis, Mederos, Luis Almaguer, Pulst, Stefan M.
Publicado 2017

A 20‐year study of suicide death in a statewide autism population

por Kirby, Anne V., Bakian, Amanda V., Zhang, Yue, Bilder, Deborah A., Keeshin, Brooks R., Coon, Hilary
Publicado 2019

Association of the CHRNA4 Neuronal Nicotinic Receptor Subunit Gene with Frequency of Binge Drinking in Young Adults

por Coon, Hilary, Piasecki, Thomas M., Cook, Edwin H., Dunn, Diane, Mermelstein, Robin J., Weiss, Robert B., Cannon, Dale S.
Publicado 2014

Severity of cough in idiopathic pulmonary fibrosis is associated with MUC5 B genotype

por Scholand, Mary Beth, Wolff, Roger, Crossno, Peter Fredrick, Sundar, Krishna, Winegar, Molly, Whipple, Spencer, Carey, Patrick, Sunchild, Nicholas, Coon, Hilary
Publicado 2014

Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders

por Cannon, Dale S, Miller, Judith S, Robison, Reid J, Villalobos, Michele E, Wahmhoff, Natalie K, Allen-Brady, Kristina, McMahon, William M, Coon, Hilary
Publicado 2010

Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees

por Coon, Hilary, Villalobos, Michele E, Robison, Reid J, Camp, Nicola J, Cannon, Dale S, Allen-Brady, Kristina, Miller, Judith S, McMahon, William M
Publicado 2010

Genome-wide association study meta-analysis of suicide death and suicidal behavior

por Li, Qingqin S., Shabalin, Andrey A., DiBlasi, Emily, Gopal, Srihari, Canuso, Carla M., Palotie, Aarno, Drevets, Wayne C., Docherty, Anna R., Coon, Hilary
Publicado 2022

Altered transcriptomes, cell type proportions, and dendritic spine morphology in hippocampus of suicide deaths

por Das, Sujan C., Schulmann, Anton, Callor, William B., Jerominski, Leslie, Panicker, Mitradas M., Christensen, Erik D., Bunney, William E., Williams, Megan E., Coon, Hilary, Vawter, Marquis P.
Publicado 2023

Allele-specific expression in a family quartet with autism reveals mono-to-biallelic switch and novel transcriptional processes of autism susceptibility genes

por Lin, Chun-Yen, Chang, Kai-Wei, Lin, Chia-Yi, Wu, Jia-Ying, Coon, Hilary, Huang, Pei-Hsin, Ho, Hong-Nerng, Akbarian, Schahram, Gau, Susan Shur-Fen, Huang, Hsien-Sung
Publicado 2018

Assessment of suicide attempt and death in bipolar affective disorder: a combined clinical and genetic approach

por Monson, Eric T., Shabalin, Andrey A., Docherty, Anna R., DiBlasi, Emily, Bakian, Amanda V., Li, Qingqin S., Gray, Douglas, Keeshin, Brooks, Crowell, Sheila E., Mullins, Niamh, Willour, Virginia L., Coon, Hilary
Publicado 2021

Whole-genome sequencing analysis in families with recurrent pregnancy loss: A pilot study

por Workalemahu, Tsegaselassie, Avery, Cecile, Lopez, Sarah, Blue, Nathan R., Wallace, Amelia, Quinlan, Aaron R., Coon, Hilary, Warner, Derek, Varner, Michael W., Branch, D. Ware, Jorde, Lynn B., Silver, Robert M.
Publicado 2023

A population-wide analysis of the familial risk of suicide in Utah, USA

por Bakian, Amanda V., Chen, Danli, Zhang, Chong, Hanson, Heidi A., Docherty, Anna R., Keeshin, Brooks, Gray, Douglas, Smith, Ken R., VanDerslice, James A., Yu, David Z., Zhang, Yue, Coon, Hilary
Publicado 2023

An investigation of the effects of lipid-lowering medications: genome-wide linkage analysis of lipids in the HyperGEN study

por Wu, Jun, Province, Michael A, Coon, Hilary, Hunt, Steven C, Eckfeldt, John H, Arnett, Donna K, Heiss, Gerardo, Lewis, Cora E, Ellison, R Curtis, Rao, Dabeeru C, Rice, Treva, Kraja, Aldi T
Publicado 2007

Neurexin 1 variants as risk factors for suicide death

por William, Nancy, Reissner, Carsten, Sargent, Robert, Darlington, Todd M., DiBlasi, Emily, Li, Qingqin S., Keeshin, Brooks, Callor, William B., Ferris, Elliott, Jerominski, Leslie, Smith, Ken R., Christensen, Erik D., Gray, Douglas M., Camp, Nicola J., Missler, Markus, Williams, Megan E., Coon, Hilary
Publicado 2021

Extended familial risk of suicide death is associated with younger age at death and elevated polygenic risk of suicide

por Coon, Hilary, Shabalin, Andrey, Bakian, Amanda V., DiBlasi, Emily, Monson, Eric T., Kirby, Anne, Chen, Danli, Fraser, Alison, Yu, Zhe, Staley, Michael, Callor, William Brandon, Christensen, Erik D., Crowell, Sheila E., Gray, Douglas, Crockett, David K., Li, Qingqin S., Keeshin, Brooks, Docherty, Anna R.
Publicado 2022

The role of rare compound heterozygous events in autism spectrum disorder

por Lin, Bochao Danae, Colas, Fabrice, Nijman, Isaac J., Medic, Jelena, Brands, William, Parr, Jeremy R., van Eijk, Kristel R., Klauck, Sabine M., Chiocchetti, Andreas G., Freitag, Christine M., Maestrini, Elena, Bacchelli, Elena, Coon, Hilary, Vicente, Astrid, Oliveira, Guiomar, Pagnamenta, Alistair T., Gallagher, Louise, Ennis, Sean, Anney, Richard, Bourgeron, Thomas, Luykx, Jurjen J., Vorstman, Jacob
Publicado 2020

A Candidate Gene Approach Identifies the CHRNA5-A3-B4 Region as a Risk Factor for Age-Dependent Nicotine Addiction

por Weiss, Robert B., Baker, Timothy B., Cannon, Dale S., von Niederhausern, Andrew, Dunn, Diane M., Matsunami, Nori, Singh, Nanda A., Baird, Lisa, Coon, Hilary, McMahon, William M., Piper, Megan E., Fiore, Michael C., Scholand, Mary Beth, Connett, John E., Kanner, Richard E., Gahring, Lorise C., Rogers, Scott W., Hoidal, John R., Leppert, Mark F.
Publicado 2008

The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses

por Buxbaum, Joseph D, Bolshakova, Nadia, Brownfeld, Jessica M, Anney, Richard JL, Bender, Patrick, Bernier, Raphael, Cook, Edwin H, Coon, Hilary, Cuccaro, Michael, Freitag, Christine M, Hallmayer, Joachim, Geschwind, Daniel, Klauck, Sabine M, Nurnberger, John I, Oliveira, Guiomar, Pinto, Dalila, Poustka, Fritz, Scherer, Stephen W, Shih, Andy, Sutcliffe, James S, Szatmari, Peter, Vicente, Astrid M, Vieland, Veronica, Gallagher, Louise
Publicado 2014

Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide

por Coon, Hilary, Darlington, Todd M., DiBlasi, Emily, Callor, W. Brandon, Ferris, Elliott, Fraser, Alison, Yu, Zhe, William, Nancy, Das, Sujan C., Crowell, Sheila E., Chen, Danli, Anderson, John S., Klein, Michael, Jerominski, Leslie, Cannon, Dale, Shabalin, Andrey, Docherty, Anna, Williams, Megan, Smith, Ken R., Keeshin, Brooks, Bakian, Amanda V., Christensen, Erik, Li, Qingqin S., Camp, Nicola J., Gray, Douglas
Publicado 2018