Critical Role for the DNA Sensor AIM2 in Stem Cell Proliferation and Cancer
Man, Si Ming, Zhu, Qifan, Zhu, Liqin, Liu, Zhiping, Karki, Rajendra, Malik, Ankit, Sharma, Deepika, Li, Liyuan, Malireddi, R.K. Subbarao, Gurung, Prajwal, Neale, Geoffrey, Olsen, Scott R., Carter, Robert A., McGoldrick, Daniel J., Wu, Gang, Finkelstein, David, Vogel, Peter, Gilbertson, Richard J., Kanneganti, Thirumala-Devi
Published in Cell (02.07.2015)
Published in Cell (02.07.2015)
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Dietary modulation of the microbiome affects autoinflammatory disease
Lukens, John R., Gurung, Prajwal, Vogel, Peter, Johnson, Gordon R., Carter, Robert A., McGoldrick, Daniel J., Bandi, Srinivasa Rao, Calabrese, Christopher R., Walle, Lieselotte Vande, Lamkanfi, Mohamed, Kanneganti, Thirumala-Devi
Published in Nature (London) (11.12.2014)
Published in Nature (London) (11.12.2014)
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Control of virulence by small RNAs in Streptococcus pneumoniae
Mann, Beth, van Opijnen, Tim, Wang, Jianmin, Obert, Caroline, Wang, Yong-Dong, Carter, Robert, McGoldrick, Daniel J, Ridout, Granger, Camilli, Andrew, Tuomanen, Elaine I, Rosch, Jason W
Published in PLoS pathogens (01.07.2012)
Published in PLoS pathogens (01.07.2012)
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Social Interest Data as a Proxy for Off-Label Performance-Enhancing Drug Use: Implications and Clinical Considerations
Holubeck, Philip A, Eksi, Andrew C, Gillett, Kyle, O'Hara, James, McGoldrick, Daniel J, Brown, Demi R, McCarthy, Alec D
Published in Curēus (Palo Alto, CA) (01.01.2024)
Published in Curēus (Palo Alto, CA) (01.01.2024)
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Social Data: An Underutilized Metric for Determining Participation in COVID-19 Vaccinations
McCarthy, Alec D, McGoldrick, Daniel J, Holubeck, Phil A, Cohoes, Cavan, Bilek, Laura D
Published in Curēus (Palo Alto, CA) (14.07.2021)
Published in Curēus (Palo Alto, CA) (14.07.2021)
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MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder
Heimer, Gali, Kerätär, Juha M., Riley, Lisa G., Balasubramaniam, Shanti, Eyal, Eran, Pietikäinen, Laura P., Hiltunen, J. Kalervo, Marek-Yagel, Dina, Hamada, Jeffrey, Gregory, Allison, Rogers, Caleb, Hogarth, Penelope, Nance, Martha A., Shalva, Nechama, Veber, Alvit, Tzadok, Michal, Nissenkorn, Andreea, Tonduti, Davide, Renaldo, Florence, Bamshad, Michael J., Leal, Suzanne M., Nickerson, Deborah A., Anderson, Peter, Annable, Marcus, Blue, Elizabeth Marchani, Buckingham, Kati J., Chin, Jennifer, Chong, Jessica X., Cornejo, Rodolfo, Davis, Colleen P., Frazar, Christopher, He, Zongxiao, Jarvik, Gail P., Jimenez, Guillaume, Johanson, Eric, Kolar, Tom, Krauter, Stephanie A., Luksic, Daniel, Marvin, Colby T., McGee, Sean, McGoldrick, Daniel J., Patterson, Karynne, Perez, Marcos, Phillips, Sam W., Pijoan, Jessica, Robertson, Peggy D., Santos-Cortez, Regie, Shankar, Aditi, Slattery, Krystal, Shively, Kathryn M., Siegel, Deborah L., Smith, Joshua D., Tackett, Monica, Wang, Gao, Wegener, Marc, Weiss, Jeffrey M., Wernick, Riana I., Wheeler, Marsha M., Yi, Qian, Kraoua, Ichraf, Panteghini, Celeste, Valletta, Lorella, Garavaglia, Barbara, Cowley, Mark J., Gayevskiy, Velimir, Roscioli, Tony, Silberstein, Jonathon M., Hoffmann, Chen, Raas-Rothschild, Annick, Tiranti, Valeria, Anikster, Yair, Christodoulou, John, Kastaniotis, Alexander J., Ben-Zeev, Bruria, Hayflick, Susan J.
Published in American journal of human genetics (01.12.2016)
Published in American journal of human genetics (01.12.2016)
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Precision medicine for developmental and epileptic encephalopathies in Africa—strategies for a resource-limited setting
Esterhuizen, Alina I., Tiffin, Nicki, Riordan, Gillian, Wessels, Marie, Burman, Richard J., Aziz, Miriam C., Calhoun, Jeffrey D., Gunti, Jonathan, Amiri, Ezra E., Ramamurthy, Aishwarya, Bamshad, Michael J., Bamshad, Michael J., Leal, Suzanne M., Nickerson, Deborah A., Anderson, Peter, Bacus, Tamara J., Blue, Elizabeth E., Brower, Katherine, Buckingham, Kati J., Chong, Jessica X., Cornejo Sánchez, Diana, Davis, Colleen P., Davis, Chayna J., Frazar, Christian D., Gomeztagle-Burgess, Katherine, Gordon, William W., Horike-Pyne, Martha, Hurless, Jameson R., Jarvik, Gail P., Johanson, Eric, Thomas Kolar, J., Marvin, Colby T., McGee, Sean, McGoldrick, Daniel J., Mekonnen, Betselote, Nielsen, Patrick M., Patterson, Karynne, Radhakrishnan, Aparna, Richardson, Matthew A., Roote, Gwendolin T., Ryke, Erica L., Schrauwen, Isabelle, Shively, Kathryn M., Smith, Joshua D., Tackett, Monica, Wang, Gao, Weiss, Jeffrey M., Wheeler, Marsha M., Yi, Qian, Zhang, Xiaohong, Mefford, Heather C., Ramesar, Raj, Wilmshurst, Jo M., Carvill, Gemma L.
Published in Genetics in medicine (01.02.2023)
Published in Genetics in medicine (01.02.2023)
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Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance
Liaqat, Khurram, Schrauwen, Isabelle, Raza, Syed Irfan, Lee, Kwanghyuk, Hussain, Shabir, Chakchouk, Imen, Nasir, Abdul, Acharya, Anushree, Abbe, Izoduwa, Umair, Muhammad, Ansar, Muhammad, Ullah, Irfan, Shah, Khadim, Bamshad, Michael J, Nickerson, Deborah A, Ahmad, Wasim, Leal, Suzanne M
Published in Journal of human genetics (01.02.2019)
Published in Journal of human genetics (01.02.2019)
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Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment
Schrauwen, Isabelle, Chakchouk, Imen, Acharya, Anushree, Liaqat, Khurram, Irfanullah, Nickerson, Deborah A, Bamshad, Michael J, Shah, Khadim, Ahmad, Wasim, Leal, Suzanne M
Published in BMC medical genetics (20.07.2018)
Published in BMC medical genetics (20.07.2018)
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