Methamphetamine-Induced Sleep Impairments and Subsequent Slow-Wave and Rapid Eye Movement Sleep Rebound in Male Rhesus Monkeys

por Berro, Laís F., Overton, John S., Rowlett, James K.
Publicado 2022

In silico mutagenesis: a case study of the melanocortin 4 receptor

por Bromberg, Yana, Overton, John, Vaisse, Christian, Leibel, Rudolph L., Rost, Burkhard
Publicado 2009

Epidemiology of DYT1 dystonia: Estimating prevalence via genetic ascertainment

por Park, Joseph, Damrauer, Scott M., Baras, Aris, Reid, Jeffrey G., Overton, John D., Gonzalez-Alegre, Pedro
Publicado 2019

Causal Effect of Adiposity Measures on Blood Pressure Traits in 2 Urban Swedish Cohorts: A Mendelian Randomization Study

por Giontella, Alice, Lotta, Luca A., Overton, John D., Baras, Aris, Minuz, Pietro, Melander, Olle, Gill, Dipender, Fava, Cristiano
Publicado 2021

Association of Thyroid Function with Blood Pressure and Cardiovascular Disease: A Mendelian Randomization

por Giontella, Alice, Lotta, Luca A., Overton, John D., Baras, Aris, Sartorio, Andrea, Minuz, Pietro, Gill, Dipender, Melander, Olle, Fava, Cristiano
Publicado 2021

Flexible and scalable genotyping-by-sequencing strategies for population studies

por Heffelfinger, Christopher, Fragoso, Christopher A, Moreno, Maria A, Overton, John D, Mottinger, John P, Zhao, Hongyu, Tohme, Joe, Dellaporta, Stephen L
Publicado 2014

CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing data

por Packer, Jonathan S., Maxwell, Evan K., O’Dushlaine, Colm, Lopez, Alexander E., Dewey, Frederick E., Chernomorsky, Rostislav, Baras, Aris, Overton, John D., Habegger, Lukas, Reid, Jeffrey G.
Publicado 2016

Large-scale exome datasets reveal a new class of adaptor-related protein complex 2 sigma subunit (AP2σ) mutations, located at the interface with the AP2 alpha subunit, that impair...

por Gorvin, Caroline M, Metpally, Raghu, Stokes, Victoria J, Hannan, Fadil M, Krishnamurthy, Sarath B, Overton, John D, Reid, Jeffrey G, Breitwieser, Gerda E, Thakker, Rajesh V
Publicado 2018

Somatic HRAS p.G12S Mutation Causes Woolly Hair and Epidermal Nevi

por Levinsohn, Jonathan L., Teng, Joyce, Craiglow, Brittany G., Loring, Erin C., Burrow, T. Andrew, Mane, Shrikant S., Overton, John D., Lifton, Richard P., McNiff, Jennifer M., Lucky, Anne W., Choate, Keith A.
Publicado 2013

UGT1A1 genetic variants are associated with increases in bilirubin levels in rheumatoid arthritis patients treated with sarilumab

por Lin, Nan, Damask, Amy, Boyapati, Anita, Hamilton, Jennifer D., Hamon, Sara, Ternes, Nils, Nivens, Michael C., Penn, John, Lopez, Alexander, Reid, Jeffrey G., Overton, John, Shuldiner, Alan R., Abecasis, Goncalo, Baras, Aris, Paulding, Charles
Publicado 2022

Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation

por Romberg, Neil, Al Moussawi, Khatoun, Nelson-Williams, Carol, Stiegler, Amy L, Loring, Erin, Choi, Murim, Overton, John, Meffre, Eric, Khokha, Mustafa K, Huttner, Anita J, West, Brian, Podoltsev, Nikolai A, Boggon, Titus J, Kazmierczak, Barbara I, Lifton, Richard P
Publicado 2014

Whole exome sequencing reveals somatic mutations in HRAS and KRAS which cause nevus sebaceus

por Levinsohn, Jonathan L., Tian, Li C., Boyden, Lynn M., McNiff, Jennifer M., Narayan, Deepak, Loring, Erin S., Yun, Duri, Sugarman, Jeffrey L., Overton, John D., Mane, Shrikant M., Lifton, Richard P., Paller, Amy S., Wagner, Annette M., Antaya, Richard J., Choate, Keith A.
Publicado 2012

Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn’s Disease

por Horowitz, Julie E., Warner, Neil, Staples, Jeffrey, Crowley, Eileen, Gosalia, Nehal, Murchie, Ryan, Van Hout, Cristopher, Fiedler, Karoline, Welch, Gabriel, King, Alejandra Klauer, Reid, Jeffrey G., Overton, John D., Baras, Aris, Shuldiner, Alan R., Griffiths, Anne, Gottesman, Omri, Muise, Aleixo M., Gonzaga-Jauregui, Claudia
Publicado 2021

ERAP1, ERAP2, and Two Copies of HLA-Aw19 Alleles Increase the Risk for Birdshot Chorioretinopathy in HLA-A29 Carriers

por Gelfman, Sahar, Monnet, Dominique, Ligocki, Ann J., Tabary, Thierry, Moscati, Arden, Bai, Xiaodong, Freudenberg, Jan, Cooper, Blerta, Kosmicki, Jack A., Wolf, Sarah, Ferreira, Manuel A. R., Overton, John, Weyne, Jonathan, Stahl, Eli A., Baras, Aris, Romano, Carmelo, Cohen, Jacques H. M., Coppola, Giovanni, Brézin, Antoine
Publicado 2021

Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations

por Kranzler, Henry R., Zhou, Hang, Kember, Rachel L., Vickers Smith, Rachel, Justice, Amy C., Damrauer, Scott, Tsao, Philip S., Klarin, Derek, Baras, Aris, Reid, Jeffrey, Overton, John, Rader, Daniel J., Cheng, Zhongshan, Tate, Janet P., Becker, William C., Concato, John, Xu, Ke, Polimanti, Renato, Zhao, Hongyu, Gelernter, Joel
Publicado 2019

Author Correction: Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations

por Kranzler, Henry R., Zhou, Hang, Kember, Rachel L., Smith, Rachel Vickers, Justice, Amy C., Damrauer, Scott, Tsao, Philip S., Klarin, Derek, Baras, Aris, Reid, Jeffrey, Overton, John, Rader, Daniel J., Cheng, Zhongshan, Tate, Janet P., Becker, William C., Concato, John, Xu, Ke, Polimanti, Renato, Zhao, Hongyu, Gelernter, Joel
Publicado 2019

Author Correction: Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations

por Kranzler, Henry R., Zhou, Hang, Kember, Rachel L., Smith, Rachel Vickers, Justice, Amy C., Damrauer, Scott, Tsao, Philip S., Klarin, Derek, Baras, Aris, Reid, Jeffrey, Overton, John, Rader, Daniel J., Cheng, Zhongshan, Tate, Janet P., Becker, William C., Concato, John, Xu, Ke, Polimanti, Renato, Zhao, Hongyu, Gelernter, Joel
Publicado 2019

Positional Cloning of “Lisch-like”, a Candidate Modifier of Susceptibility to Type 2 Diabetes in Mice

por Dokmanovic-Chouinard, Marija, Chung, Wendy K., Chevre, Jean-Claude, Watson, Elizabeth, Yonan, Jason, Wiegand, Beebe, Bromberg, Yana, Wakae, Nao, Wright, Chris V., Overton, John, Ghosh, Sujoy, Sathe, Ganesh M., Ammala, Carina E., Brown, Kathleen K., Ito, Rokuro, LeDuc, Charles, Solomon, Keely, Fischer, Stuart G., Leibel, Rudolph L.
Publicado 2008

Genome‐wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals

por Gao, Chuan, Marcketta, Anthony, Backman, Joshua D., O'Dushlaine, Colm, Staples, Jeffrey, Ferreira, Manuel Allen Revez, Lotta, Luca A., Overton, John D., Reid, Jeffrey G., Mirshahi, Tooraj, Regeneron Genetics Center, Geisinger Regeneron Discovehr Collaboration, Baras, Aris, Abecasis, Gonçalo, Shuldiner, Alan R., Van Hout, Cristopher V., McCarthy, Shane
Publicado 2021

Genomic landscape of cutaneous T cell lymphoma

por Choi, Jaehyuk, Goh, Gerald, Walradt, Trent, Hong, Bok S., Bunick, Christopher G., Chen, Kan, Bjornson, Robert D., Maman, Yaakov, Wang, Tiffany, Tordoff, Jesse, Carlson, Kacie, Overton, John D., Liu, Kristina J., Lewis, Julia M., Devine, Lesley, Barbarotta, Lisa, Foss, Francine M., Subtil, Antonio, Vonderheid, Eric C., Edelson, Richard L., Schatz, David G., Boggon, Titus J., Girardi, Michael, Lifton, Richard P.
Publicado 2015