Applying multiple frameworks to establish effective virtual collaborative teams in academia: a review and recommendations

por Crites, Gerald E, Berry, Andrea, Hall, Elissa, Kay, Denise, Khalil, Mohammed K, Hurtubise, Larry
Publicado 2020

OR24-6 Non-syndromic Cushing's Disease Due To CDKN1B Mutations: Novel Mutations And Phenotypic Features In A Large Pediatric Cohort

por Hernández-Ramírez, Laura, Chasseloup, Fanny, Faucz, Fabio, Lodish, Maya, Pankratz, Nathan, Chittiboina, Prashant, Lane, John, Kay, Denise, Mills, James, Stratakis, Constantine
Publicado 2019

Validation of a Custom Next-Generation Sequencing Assay for Cystic Fibrosis Newborn Screening

por Sicko, Robert J., Stevens, Colleen F., Hughes, Erin E., Leisner, Melissa, Ling, Helen, Saavedra-Matiz, Carlos A., Caggana, Michele, Kay, Denise M.
Publicado 2021

RF01 | PMON167 Isolated Cushing's Disease Associated With Rare Germline SDHx Variants

por Chittiboina, Prashant, Kay, Denise M, Mills, James L, Stratakis, Constantine A, Hernãndez-Ramírez, Laura C, Pankratz, Nathan, Lane, John, Faucz, Fabio R
Publicado 2022

Utility of Newborn Dried Blood Spots to Ascertain Seroprevalence of SARS-CoV-2 Antibodies Among Individuals Giving Birth in New York State, November 2019 to November 2021

por Damjanovic, Amanda, Styer, Linda M., Nemeth, Katherine, Yauney, Erica, Rock, Jean M., Bievenue, Rachel, Hoen, Rebecca, Ehrbar, Dylan, Kay, Denise M., Caggana, Michele, Parker, Monica M.
Publicado 2022

Multiple Lines of Evidence Risk Assessment of Terrestrial Passerines Exposed to PCDFs and PCDDs in the Tittabawassee River Floodplain, Midland, Michigan, USA

por Fredricks, Timothy B., Giesy, John P., Coefield, Sarah J., Seston, Rita M., Tazelaar, Dustin L., Roark, Shaun A., Kay, Denise P., Newsted, John L., Zwiernik, Matthew J.
Publicado 2011

Reproductive success of three passerine species exposed to dioxin-like compounds near Midland, Michigan, USA

por Fredricks, Timothy B., Zwiernik, Matthew J., Seston, Rita M., Coefield, Sarah J., Glaspie, Cassandra N., Tazelaar, Dustin L., Kay, Denise P., Newsted, John L., Giesy, John P.
Publicado 2012

Passerine Exposure to Primarily PCDFs and PCDDs in the River Floodplains Near Midland, Michigan, USA

por Fredricks, Timothy B., Zwiernik, Matthew J., Seston, Rita M., Coefield, Sarah J., Plautz, Stephanie C., Tazelaar, Dustin L., Shotwell, Melissa S., Bradley, Patrick W., Kay, Denise P., Giesy, John P.
Publicado 2009

Copy number variants in Ebstein anomaly

por Giannakou, Andreas, Sicko, Robert J., Zhang, Wei, Romitti, Paul, Browne, Marilyn L., Caggana, Michele, Brody, Lawrence C., Jelliffe-Pawlowski, Laura, Shaw, Gary M., Kay, Denise M., Mills, James L.
Publicado 2017

Genetic Variants in Isolated Ebstein Anomaly Implicated in Myocardial Development Pathways

por Sicko, Robert J., Browne, Marilyn L., Rigler, Shannon L., Druschel, Charlotte M., Liu, Gang, Fan, Ruzong, Romitti, Paul A., Caggana, Michele, Kay, Denise M., Brody, Lawrence C., Mills, James L.
Publicado 2016

Corticotropinoma as a Component of Carney Complex

por Hernández-Ramírez, Laura C., Tatsi, Christina, Lodish, Maya B., Faucz, Fabio R., Pankratz, Nathan, Chittiboina, Prashant, Lane, John, Kay, Denise M., Valdés, Nuria, Dimopoulos, Aggeliki, Mills, James L., Stratakis, Constantine A.
Publicado 2017

OR2802 A Novel CABLES1 Missense Variant Associated With Cushing's Disease Disrupts Protein Structure And Stability

por Franco-Álvarez, Alexa L, Morán, Mariana Torres, Rebollar-Vega, Rosa G, Pankratz, Nathan, Lane, John, Faucz, Fabio R, Chittiboina, Prashant, Kay, Denise M, Mills, James L, Stratakis, Constantine A, Hernández-Ramírez, Laura C
Publicado 2023

Copy-number variants and candidate gene mutations in isolated split hand/foot malformation

por Carter, Tonia C., Sicko, Robert J., Kay, Denise M., Browne, Marilyn L., Romitti, Paul A., Edmunds, Zoë L., Liu, Aiyi, Fan, Ruzong, Druschel, Charlotte M., Caggana, Michele, Brody, Lawrence C., Mills, James L.
Publicado 2017

Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis

por Fadista, João, Skotte, Line, Geller, Frank, Bybjerg-Grauholm, Jonas, Gørtz, Sanne, Romitti, Paul A, Caggana, Michele, Kay, Denise M, Matsson, Hans, Boyd, Heather A, Hougaard, David M, Nordenskjöld, Agneta, Mills, James L, Melbye, Mads, Feenstra, Bjarke
Publicado 2019

Hepatic P450 Enzyme Activity, Tissue Morphology and Histology of Mink (Mustela vison) Exposed to Polychlorinated Dibenzofurans

por Moore, Jeremy N., Newsted, John L., Hecker, Markus, Zwiernik, Matthew J., Fitzgerald, Scott D., Kay, Denise P., Zhang, Xiaowei, Higley, Eric B., Aylward, Lesa L., Beckett, Kerrie J., Budinsky, Robert A., Bursian, Steven J., Giesy, John P.
Publicado 2009

A genetic basis for the variable effect of smoking/nicotine on Parkinson's disease

por Hill-Burns, Erin M., Singh, Navjot, Ganguly, Prabarna, Hamza, Taye H., Montimurro, Jennifer, Kay, Denise M., Yearout, Dora, Sheehan, Patricia, Frodey, Kevin, Mclear, Julie A., Feany, Mel B., Hanes, Steven D., Wolfgang, William J., Zabetian, Cyrus P., Factor, Stewart A., Payami, Haydeh
Publicado 2012

Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects

por Pangilinan, Faith, Molloy, Anne M, Mills, James L, Troendle, James F, Parle-McDermott, Anne, Kay, Denise M, Browne, Marilyn L, McGrath, Emily C, Abaan, Hatice Ozel, Sutton, Marie, Kirke, Peadar N, Caggana, Michele, Shane, Barry, Scott, John M, Brody, Lawrence C
Publicado 2014

Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson’s disease

por Hamza, Taye H, Zabetian, Cyrus P, Tenesa, Albert, Laederach, Alain, Montimurro, Jennifer, Yearout, Dora, Kay, Denise M, Doheny, Kimberly F, Paschall, Justin, Pugh, Elizabeth, Kusel, Victoria I, Collura, Randall, Roberts, John, Griffith, Alida, Samii, Ali, Scott, William K, Nutt, John, Factor, Stewart A, Payami, Haydeh
Publicado 2010

Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing’s disease

por Hernández-Ramírez, Laura C, Gam, Ryhem, Valdés, Nuria, Lodish, Maya B, Pankratz, Nathan, Balsalobre, Aurelio, Gauthier, Yves, Faucz, Fabio R, Trivellin, Giampaolo, Chittiboina, Prashant, Lane, John, Kay, Denise M, Dimopoulos, Aggeliki, Gaillard, Stephan, Neou, Mario, Bertherat, Jérôme, Assié, Guillaume, Villa, Chiara, Mills, James L, Drouin, Jacques, Stratakis, Constantine A
Publicado 2017

Missed Cystic Fibrosis Newborn Screening Cases due to Immunoreactive Trypsinogen Levels below Program Cutoffs: A National Survey of Risk Factors

por Kharrazi, Martin, Sacramento, Charlene, Comeau, Anne Marie, Hale, Jaime E., Caggana, Michele, Kay, Denise M., Lee, Rachel, Reilly, Brendan, Thompson, John D., Nasr, Samya Z., Kleyn, Mary, Hoffman, Gary, Baker, Mei W., Clarke, Colleen, Harris, Cheryl L., Dorley, M. Christine, Fryman, Hilary, Sutaria, Ankit, Hietala, Amy, Winslow, Holly, Richards, Holly, Therrell, Bradford L.
Publicado 2022