von Willebrand factor antigen levels are associated with burden of rare nonsynonymous variants in the VWF gene

por Sadler, Brooke, Christopherson, Pamela A., Haller, Gabe, Montgomery, Robert R., Di Paola, Jorge
Publicado 2021

Positive Selection on Loci Associated with Drug and Alcohol Dependence

por Sadler, Brooke, Haller, Gabe, Edenberg, Howard, Tischfield, Jay, Brooks, Andy, Kramer, John, Schuckit, Marc, Nurnberger, John, Goate, Alison
Publicado 2015

Rare and de novo duplications containing SHOX in clubfoot

por Sadler, Brooke, Haller, Gabe, Antunes, Lilian, Nikolov, Momchil, Amarillo, Ina, Coe, Bradley, Dobbs, Matthew B., Gurnett, Christina A.
Publicado 2020

Variants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy

por Sadler, Brooke, Haller, Gabe, Agrawal, Arpana, Culverhouse, Rob, Bucholz, Kathleen, Brooks, Andy, Tischfield, Jay, Johnson, Eric O., Edenberg, Howard, Schuckit, Marc, Saccone, Nancy, Bierut, Laura, Goate, Alison
Publicado 2014

Fine Mapping of Genetic Variants in BIN1, CLU, CR1 and PICALM for Association with Cerebrospinal Fluid Biomarkers for Alzheimer's Disease

por Kauwe, John S. K., Cruchaga, Carlos, Karch, Celeste M., Sadler, Brooke, Lee, Mo, Mayo, Kevin, Latu, Wayne, Su'a, Manti, Fagan, Anne M., Holtzman, David M., Morris, John C., Goate, Alison M.
Publicado 2011

Whole-exome analysis of adolescents with low VWF and heavy menstrual bleeding identifies novel genetic associations

por Sadler, Brooke, Minard, Charles G., Haller, Gabe, Gurnett, Christina A., O’Brien, Sarah H., Wheeler, Allison, Jain, Shilpa, Sharma, Mutka, Zia, Ayesha, Kulkarni, Roshni, Mullins, Eric, Ragni, Margaret V., Sidonio, Robert, Dietrich, Jennifer E., Kouides, Peter A., Di Paola, Jorge, Srivaths, Lakshmi
Publicado 2022

Interleukin-7 Reverses Lymphopenia and Improves T-Cell Function in Coronavirus Disease 2019 Patient With Inborn Error of Toll-Like Receptor 3: A Case Report

por Mazer, Monty B., Turnbull, Isaiah R., Miles, Sydney, Blood, Teresa M., Sadler, Brooke, Hess, Annie, Botney, Mitchell D., Martin, Robert S., Bosanquet, James P., Striker, David A., Anand, Nitin S., Morre, Michel, Caldwell, Charles C., Brakenridge, Scott C., Moldawer, Lyle L., Di Paola, Jorge A., Hotchkiss, Richard S., Remy, Kenneth E.
Publicado 2021

A missense variant in SLC39A8 is associated with severe idiopathic scoliosis

por Haller, Gabe, McCall, Kevin, Jenkitkasemwong, Supak, Sadler, Brooke, Antunes, Lilian, Nikolov, Momchil, Whittle, Julia, Upshaw, Zachary, Shin, Jimann, Baschal, Erin, Cruchaga, Carlos, Harms, Matthew, Raggio, Cathleen, Morcuende, Jose A., Giampietro, Philip, Miller, Nancy H., Wise, Carol, Gray, Ryan S., Solnica-Krezel, Lila, Knutson, Mitchell, Dobbs, Matthew B., Gurnett, Christina A.
Publicado 2018

Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders

por Yang, Chengran, Farias, Fabiana H.G., Ibanez, Laura, Suhy, Adam, Sadler, Brooke, Fernandez, Maria Victoria, Wang, Fengxian, Bradley, Joseph L., Eiffert, Brett, Bahena, Jorge A., Budde, John P., Li, Zeran, Dube, Umber, Sung, Yun Ju, Mihindukulasuriya, Kathie A., Morris, John C., Fagan, Anne M., Perrin, Richard J., Benitez, Bruno A., Rhinn, Herve, Harari, Oscar, Cruchaga, Carlos
Publicado 2021