Risk Factors for Polyvascular Involvement in Patients With Peripheral Artery Disease: A Mendelian Randomization Study

por Dikilitas, Ozan, Satterfield, Benjamin A., Kullo, Iftikhar J.
Publicado 2020

Leveraging the Electronic Health Record to Address the COVID-19 Pandemic

por Satterfield, Benjamin A., Dikilitas, Ozan, Kullo, Iftikhar J.
Publicado 2021

COMPUTED ALGORITHMS TO IDENTIFY SUBTYPES OF ACUTE MYOCARDIAL INJURY IN ACUTE COVID-19

por Satterfield, Benjamin, Alhalabi, Lubna M., Kullo, Iftikhar J.
Publicado 2022

Cardiac involvement in the long-term implications of COVID-19

por Satterfield, Benjamin A., Bhatt, Deepak L., Gersh, Bernard J.
Publicado 2021

Publisher Correction: Cardiac involvement in the long-term implications of COVID-19

por Satterfield, Benjamin A., Bhatt, Deepak L., Gersh, Bernard J.
Publicado 2021

The immunomodulating V and W proteins of Nipah virus determine disease course

por Satterfield, Benjamin A., Cross, Robert W., Fenton, Karla A., Agans, Krystle N., Basler, Christopher F., Geisbert, Thomas W., Mire, Chad E.
Publicado 2015

The differential effects of heat-shocking on the viability of spores from Bacillus anthracis, Bacillus subtilis, and Clostridium sporogenes after treatment with peracetic acid- and...

por March, Jordon K, Pratt, Michael D, Lowe, Chinn-Woan, Cohen, Marissa N, Satterfield, Benjamin A, Schaalje, Bruce, O'Neill, Kim L, Robison, Richard A
Publicado 2015

Use of Single-Injection Recombinant Vesicular Stomatitis Virus Vaccine to Protect Nonhuman Primates Against Lethal Nipah Virus Disease

por Mire, Chad E., Geisbert, Joan B., Agans, Krystle N., Versteeg, Krista M., Deer, Daniel J., Satterfield, Benjamin A., Fenton, Karla A., Geisbert, Thomas W.
Publicado 2019

Durability of a Vesicular Stomatitis Virus-Based Marburg Virus Vaccine in Nonhuman Primates

por Mire, Chad E., Geisbert, Joan B., Agans, Krystle N., Satterfield, Benjamin A., Versteeg, Krista M., Fritz, Elizabeth A., Feldmann, Heinz, Hensley, Lisa E., Geisbert, Thomas W.
Publicado 2014

Antagonism of STAT1 by Nipah virus P gene products modulates disease course but not lethal outcome in the ferret model

por Satterfield, Benjamin A., Borisevich, Viktoriya, Foster, Stephanie L., Rodriguez, Sergio E., Cross, Robert W., Fenton, Karla A., Agans, Krystle N., Basler, Christopher F., Geisbert, Thomas W., Mire, Chad E.
Publicado 2019

Pathogenic Differences between Nipah Virus Bangladesh and Malaysia Strains in Primates: Implications for Antibody Therapy

por Mire, Chad E., Satterfield, Benjamin A., Geisbert, Joan B., Agans, Krystle N., Borisevich, Viktoriya, Yan, Lianying, Chan, Yee-Peng, Cross, Robert W., Fenton, Karla A., Broder, Christopher C., Geisbert, Thomas W.
Publicado 2016

A Quadruplex Real-Time PCR Assay for the Rapid Detection and Differentiation of the Most Relevant Members of the B. pseudomallei Complex: B. mallei, B. pseudomallei, and B. thailan...

por Lowe, Chinn-Woan, Satterfield, Benjamin A., Nelson, Daniel B., Thiriot, Joseph D., Heder, Michael J., March, Jordon K., Drake, David S., Lew, Cynthia S., Bunnell, Annette J., Moore, Emily S., O'Neill, Kim L., Robison, Richard A.
Publicado 2016

Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

por Ferar, Kathleen, Hall, Taryn O., Crawford, Dana C., Rowley, Robb, Satterfield, Benjamin A., Li, Rongling, Gragert, Loren, Karlson, Elizabeth W., de Andrade, Mariza, Kullo, Iftikhar J., McCarty, Catherine A., Kho, Abel, Hayes, M. Geoffrey, Ritchie, Marylyn D., Crane, Paul K., Mirel, Daniel B., Carlson, Christopher, Connolly, John J., Hakonarson, Hakon, Crenshaw, Andrew T., Carrell, David, Luo, Yuan, Dikilitas, Ozan, Denny, Joshua C., Jarvik, Gail P., Crosslin, David R.
Publicado 2023

Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

por Ferar, Kathleen, Hall, Taryn O., Crawford, Dana C., Rowley, Robb, Satterfield, Benjamin A., Li, Rongling, Gragert, Loren, Karlson, Elizabeth W., de Andrade, Mariza, Kullo, Iftikhar J., McCarty, Catherine A., Kho, Abel, Hayes, M. Geoffrey, Ritchie, Marylyn D., Crane, Paul K., Mirel, Daniel B., Carlson, Christopher, Connolly, John J., Hakonarson, Hakon, Crenshaw, Andrew T., Carrell, David, Luo, Yuan, Dikilitas, Ozan, Denny, Joshua C., Jarvik, Gail P., Crosslin, David R.
Publicado 2023

Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrum

por Lee, David S.M., Cardone, Katie M., Zhang, David Y., Abramowitz, Sarah, DePaolo, John S., Aragam, Krishna G., Biddinger, Kiran, Conery, Mitchell, Dilitikas, Ozan, Hoffman-Andrews, Lily, Judy, Renae L., Khan, Atlas, Kulo, Iftikhar, Puckelwartz, Megan J., Reza, Nosheen, Satterfield, Benjamin A., Singhal, Pankhuri, Arany, Zoltan P., Cappola, Thomas P., Carruth, Eric, Day, Sharlene M., Do, Ron, Haggarty, Christopher M., Joseph, Jacob, McNally, Elizabeth, Nadkarni, Girish, Owens, Anjali T., Rader, Daniel J., Ritchie, Marylyn D., Sun, Yan, Voight, Benjamin F., Levin, Michael G., Damrauer, Scott M.
Publicado 2023

A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR

por Safarova, Maya S., Satterfield, Benjamin A., Fan, Xiao, Austin, Erin E., Ye, Zhan, Bastarache, Lisa, Zheng, Neil, Ritchie, Marylyn D., Borthwick, Kenneth M., Williams, Marc S., Larson, Eric B., Scrol, Aaron, Jarvik, Gail P., Crosslin, David R., Leppig, Kathleen, Rasmussen-Torvik, Laura J., Pendergrass, Sarah A., Sturm, Amy C., Namjou, Bahram, Shah, Amy Sanghavi, Carroll, Robert J., Chung, Wendy K., Wei, Wei-Qi, Feng, QiPing, Stein, C. Michael, Roden, Dan M., Manolio, Teri A., Schaid, Daniel J., Denny, Joshua C., Hebbring, Scott J., de Andrade, Mariza, Kullo, Iftikhar J.
Publicado 2019

Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network

por Pacheco, Jennifer A., Rasmussen, Luke V., Wiley, Ken, Person, Thomas Nate, Cronkite, David J., Sohn, Sunghwan, Murphy, Shawn, Gundelach, Justin H., Gainer, Vivian, Castro, Victor M., Liu, Cong, Mentch, Frank, Lingren, Todd, Sundaresan, Agnes S., Eickelberg, Garrett, Willis, Valerie, Furmanchuk, Al’ona, Patel, Roshan, Carrell, David S., Deng, Yu, Walton, Nephi, Satterfield, Benjamin A., Kullo, Iftikhar J., Dikilitas, Ozan, Smith, Joshua C., Peterson, Josh F., Shang, Ning, Kiryluk, Krzysztof, Ni, Yizhao, Li, Yikuan, Nadkarni, Girish N., Rosenthal, Elisabeth A., Walunas, Theresa L., Williams, Marc S., Karlson, Elizabeth W., Linder, Jodell E., Luo, Yuan, Weng, Chunhua, Wei, WeiQi
Publicado 2023

Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure

por Levin, Michael G., Tsao, Noah L., Singhal, Pankhuri, Liu, Chang, Vy, Ha My T., Paranjpe, Ishan, Backman, Joshua D., Bellomo, Tiffany R., Bone, William P., Biddinger, Kiran J., Hui, Qin, Dikilitas, Ozan, Satterfield, Benjamin A., Yang, Yifan, Morley, Michael P., Bradford, Yuki, Burke, Megan, Reza, Nosheen, Charest, Brian, Judy, Renae L., Puckelwartz, Megan J., Hakonarson, Hakon, Khan, Atlas, Kottyan, Leah C., Kullo, Iftikhar, Luo, Yuan, McNally, Elizabeth M., Rasmussen-Torvik, Laura J., Day, Sharlene M., Do, Ron, Phillips, Lawrence S., Ellinor, Patrick T., Nadkarni, Girish N., Ritchie, Marylyn D., Arany, Zoltan, Cappola, Thomas P., Margulies, Kenneth B., Aragam, Krishna G., Haggerty, Christopher M., Joseph, Jacob, Sun, Yan V., Voight, Benjamin F., Damrauer, Scott M.
Publicado 2022

Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases

por Georges, Adrien, Yang, Min-Lee, Berrandou, Takiy-Eddine, Bakker, Mark K., Dikilitas, Ozan, Kiando, Soto Romuald, Ma, Lijiang, Satterfield, Benjamin A., Sengupta, Sebanti, Yu, Mengyao, Deleuze, Jean-François, Dupré, Delia, Hunker, Kristina L., Kyryachenko, Sergiy, Liu, Lu, Sayoud-Sadeg, Ines, Amar, Laurence, Brummett, Chad M., Coleman, Dawn M., d’Escamard, Valentina, de Leeuw, Peter, Fendrikova-Mahlay, Natalia, Kadian-Dodov, Daniella, Li, Jun Z., Lorthioir, Aurélien, Pappaccogli, Marco, Prejbisz, Aleksander, Smigielski, Witold, Stanley, James C., Zawistowski, Matthew, Zhou, Xiang, Zöllner, Sebastian, Amouyel, Philippe, De Buyzere, Marc L., Debette, Stéphanie, Dobrowolski, Piotr, Drygas, Wojciech, Gornik, Heather L., Olin, Jeffrey W., Piwonski, Jerzy, Rietzschel, Ernst R., Ruigrok, Ynte M., Vikkula, Miikka, Warchol Celinska, Ewa, Januszewicz, Andrzej, Kullo, Iftikhar J., Azizi, Michel, Jeunemaitre, Xavier, Persu, Alexandre, Kovacic, Jason C., Ganesh, Santhi K., Bouatia-Naji, Nabila
Publicado 2021

Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases

por Georges, Adrien, Yang, Min-Lee, Berrandou, Takiy-Eddine, Bakker, Mark K., Dikilitas, Ozan, Kiando, Soto Romuald, Ma, Lijiang, Satterfield, Benjamin A., Sengupta, Sebanti, Yu, Mengyao, Deleuze, Jean-François, Dupré, Delia, Hunker, Kristina L., Kyryachenko, Sergiy, Liu, Lu, Sayoud-Sadeg, Ines, Amar, Laurence, Brummett, Chad M., Coleman, Dawn M., d’Escamard, Valentina, de Leeuw, Peter, Fendrikova-Mahlay, Natalia, Kadian-Dodov, Daniella, Li, Jun Z., Lorthioir, Aurélien, Pappaccogli, Marco, Prejbisz, Aleksander, Smigielski, Witold, Stanley, James C., Zawistowski, Matthew, Zhou, Xiang, Zöllner, Sebastian, Amouyel, Philippe, De Buyzere, Marc L., Debette, Stéphanie, Dobrowolski, Piotr, Drygas, Wojciech, Gornik, Heather L., Olin, Jeffrey W., Piwonski, Jerzy, Rietzschel, Ernst R., Ruigrok, Ynte M., Vikkula, Miikka, Warchol Celinska, Ewa, Januszewicz, Andrzej, Kullo, Iftikhar J., Azizi, Michel, Jeunemaitre, Xavier, Persu, Alexandre, Kovacic, Jason C., Ganesh, Santhi K., Bouatia-Naji, Nabila
Publicado 2022