Addressing the routine failure to clinically identify monogenic cases of common disease

por Murray, Michael F., Khoury, Muin J., Abul-Husn, Noura S.
Publicado 2022

An Emerging Role for the Delta Opioid Receptor in the Regulation of Mu Opioid Receptor Function

por Rozenfeld, Raphael, Abul-Husn, Noura S., Gomez, Ivone, Devi, Lakshmi A.
Publicado 2007

Implementation and utilization of genetic testing in personalized medicine

por Abul-Husn, Noura S, Owusu Obeng, Aniwaa, Sanderson, Saskia C, Gottesman, Omri, Scott, Stuart A
Publicado 2014

Genomic Screening Identifies Individuals at High Risk for Hereditary Transthyretin Amyloidosis

por Soper, Emily R., Suckiel, Sabrina A., Braganza, Giovanna T., Kontorovich, Amy R., Kenny, Eimear E., Abul-Husn, Noura S.
Publicado 2021

The intersection of genetics and COVID-19 in 2021: preview of the 2021 Rodney Howell Symposium

por Rasmussen, Sonja A., Abul-Husn, Noura S., Casanova, Jean-Laurent, Daly, Mark J., Rehm, Heidi L., Murray, Michael F.
Publicado 2021

COVID-19 outcomes and the human genome

por Murray, Michael F., Kenny, Eimear E., Ritchie, Marylyn D., Rader, Daniel J., Bale, Allen E., Giovanni, Monica A., Abul-Husn, Noura S.
Publicado 2020

Perspectives of diverse Spanish- and English-speaking patients on the clinical use of polygenic risk scores

por Suckiel, Sabrina A., Braganza, Giovanna T., Aguiñiga, Karla López, Odgis, Jacqueline A., Bonini, Katherine E., Kenny, Eimear E., Hamilton, Jada G., Abul-Husn, Noura S.
Publicado 2022

Chronic Morphine Alters the Presynaptic Protein Profile: Identification of Novel Molecular Targets Using Proteomics and Network Analysis

por Abul-Husn, Noura S., Annangudi, Suresh P., Ma'ayan, Avi, Ramos-Ortolaza, Dinah L., Stockton, Steven D., Gomes, Ivone, Sweedler, Jonathan V., Devi, Lakshmi A.
Publicado 2011

SNAVI: Desktop application for analysis and visualization of large-scale signaling networks

por Ma'ayan, Avi, Jenkins, Sherry L, Webb, Ryan L, Berger, Seth I, Purushothaman, Sudarshan P, Abul-Husn, Noura S, Posner, Jeremy M, Flores, Tony, Iyengar, Ravi
Publicado 2009

Physician Attitudes toward Adopting Genome-Guided Prescribing through Clinical Decision Support

por Overby, Casey Lynnette, Erwin, Angelika Ludtke, Abul-Husn, Noura S., Ellis, Stephen B., Scott, Stuart A., Obeng, Aniwaa Owusu, Kannry, Joseph L., Hripcsak, George, Bottinger, Erwin P., Gottesman, Omri
Publicado 2014

Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank

por Abul-Husn, Noura S., Soper, Emily R., Odgis, Jacqueline A., Cullina, Sinead, Bobo, Dean, Moscati, Arden, Rodriguez, Jessica E., Loos, Ruth J. F., Cho, Judy H., Belbin, Gillian M., Suckiel, Sabrina A., Kenny, Eimear E.
Publicado 2019

Admixture mapping of peripheral artery disease in a Dominican population reveals a putative risk locus on 2q35

por Cullina, Sinead, Wojcik, Genevieve L., Shemirani, Ruhollah, Klarin, Derek, Gorman, Bryan R., Sorokin, Elena P., Gignoux, Christopher R., Belbin, Gillian M., Pyarajan, Saiju, Asgari, Samira, Tsao, Philip S., Damrauer, Scott M., Abul-Husn, Noura S., Kenny, Eimear E.
Publicado 2023

Implementing genomic screening in diverse populations

por Abul-Husn, Noura S., Soper, Emily R., Braganza, Giovanna T., Rodriguez, Jessica E., Zeid, Natasha, Cullina, Sinead, Bobo, Dean, Moscati, Arden, Merkelson, Amanda, Loos, Ruth J. F., Cho, Judy H., Belbin, Gillian M., Suckiel, Sabrina A., Kenny, Eimear E.
Publicado 2021

GenomeDiver: A platform for phenotype-guided medical genomic diagnosis.

por Pearson, Nathaniel M., Stolte, Christian, Shi, Kevin, Beren, Faygel, Abul-Husn, Noura S., Bertier, Gabrielle, Brown, Kaitlyn, Diaz, George A., Odgis, Jacqueline A., Suckiel, Sabrina A., Horowitz, Carol R., Wasserstein, Melissa, Gelb, Bruce D., Kenny, Eimear E., Gagnon, Charles, Jobanputra, Vaidehi, Bloom, Toby, Greally, John M.
Publicado 2021

The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse families

por Suckiel, Sabrina A., Kelly, Nicole R., Odgis, Jacqueline A., Gallagher, Katie M., Sebastin, Monisha, Bonini, Katherine E., Marathe, Priya N., Brown, Kaitlyn, Di Biase, Miranda, Ramos, Michelle A., Rodriguez, Jessica E., Scarimbolo, Laura, Insel, Beverly J., Ferar, Kathleen D.M., Zinberg, Randi E., Diaz, George A., Greally, John M., Abul-Husn, Noura S., Bauman, Laurie J., Gelb, Bruce D., Horowitz, Carol R., Wasserstein, Melissa P., Kenny, Eimear E.
Publicado 2023

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

por Abul-Husn, Noura S., Marathe, Priya N., Kelly, Nicole R., Bonini, Katherine E., Sebastin, Monisha, Odgis, Jacqueline A., Abhyankar, Avinash, Brown, Kaitlyn, Di Biase, Miranda, Gallagher, Katie M., Guha, Saurav, Ioele, Nicolette, Okur, Volkan, Ramos, Michelle A., Rodriguez, Jessica E., Rehman, Atteeq U., Thomas-Wilson, Amanda, Edelmann, Lisa, Zinberg, Randi E., Diaz, George A., Greally, John M., Jobanputra, Vaidehi, Suckiel, Sabrina A., Horowitz, Carol R., Wasserstein, Melissa P., Kenny, Eimear E., Gelb, Bruce D.
Publicado 2023

Genetic identification of a common collagen disease in Puerto Ricans via identity-by-descent mapping in a health system

por Belbin, Gillian Morven, Odgis, Jacqueline, Sorokin, Elena P, Yee, Muh-Ching, Kohli, Sumita, Glicksberg, Benjamin S, Gignoux, Christopher R, Wojcik, Genevieve L, Van Vleck, Tielman, Jeff, Janina M, Linderman, Michael, Schurmann, Claudia, Ruderfer, Douglas, Cai, Xiaoqiang, Merkelson, Amanda, Justice, Anne E, Young, Kristin L, Graff, Misa, North, Kari E, Peters, Ulrike, James, Regina, Hindorff, Lucia, Kornreich, Ruth, Edelmann, Lisa, Gottesman, Omri, Stahl, Eli EA, Cho, Judy H, Loos, Ruth JF, Bottinger, Erwin P, Nadkarni, Girish N, Abul-Husn, Noura S, Kenny, Eimear E
Publicado 2017

Artificial Intelligence and Early Detection of Pancreatic Cancer: 2020 Summative Review

por Kenner, Barbara, Chari, Suresh T., Kelsen, David, Klimstra, David S., Pandol, Stephen J., Rosenthal, Michael, Rustgi, Anil K., Taylor, James A., Yala, Adam, Abul-Husn, Noura, Andersen, Dana K., Bernstein, David, Brunak, Søren, Canto, Marcia Irene, Eldar, Yonina C., Fishman, Elliot K., Fleshman, Julie, Go, Vay Liang W., Holt, Jane M., Field, Bruce, Goldberg, Ann, Hoos, William, Iacobuzio-Donahue, Christine, Li, Debiao, Lidgard, Graham, Maitra, Anirban, Matrisian, Lynn M., Poblete, Sung, Rothschild, Laura, Sander, Chris, Schwartz, Lawrence H., Shalit, Uri, Srivastava, Sudhir, Wolpin, Brian
Publicado 2021

GUÍA: a digital platform to facilitate result disclosure in genetic counseling

por Suckiel, Sabrina A., Odgis, Jaqueline A., Gallagher, Katie M., Rodriguez, Jessica E., Watnick, Dana, Bertier, Gabrielle, Sebastin, Monisha, Yelton, Nicole, Maria, Estefany, Lopez, Jessenia, Ramos, Michelle, Kelly, Nicole, Teitelman, Nehama, Beren, Faygel, Kaszemacher, Tom, Davis, Kojo, Laguerre, Irma, Richardson, Lynne D., Diaz, George A., Pearson, Nathaniel M., Ellis, Stephen B., Stolte, Christian, Robinson, Mimsie, Kovatch, Patricia, Horowitz, Carol R., Gelb, Bruce D., Greally, John M., Bauman, Laurie J., Zinberg, Randi E., Abul-Husn, Noura S., Wasserstein, Melissa P., Kenny, Eimear E.
Publicado 2021

Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants

por Buchanan, Adam H, Manickam, Kandamurugu, Meyer, Michelle N, Wagner, Jennifer K, Hallquist, Miranda L G, Williams, Janet L, Rahm, Alanna Kulchak, Williams, Marc S, Chen, Zong-Ming E, Shah, Chaitali K, Garg, Tullika K, Lazzeri, Amanda L, Schwartz, Marci L B, Lindbuchler, D'Andra M, Fan, Audrey L, Leeming, Rosemary, Servano, Pedro O, Smith, Ashlee L, Vogel, Victor G, Abul-Husn, Noura S, Dewey, Frederick E, Lebo, Matthew S, Mason-Suares, Heather M, Ritchie, Marylyn D, Davis, F Daniel, Carey, David J, Feinberg, David T, Faucett, W Andrew, Ledbetter, David H, Murray, Michael F
Publicado 2017