Trans-ethnic genome-wide association studies: advantages and challenges of mapping in diverse populations

Por Li, Yun R, Keating, Brendan J
Publicado no Genome Med (2014)

Stress granules as crucibles of ALS pathogenesis

Por Li, Yun R., King, Oliver D., Shorter, James, Gitler, Aaron D.
Publicado em 2013

Making the genomic leap in HCT: application of second-generation sequencing to clinical advances in hematopoietic cell transplantation

Por Li, Yun R, Levine, John E, Hakonarson, Hakon, Keating, Brendan J
Publicado em 2014

Human olfactory receptor responses to odorants

Por Mainland, Joel D, Li, Yun R, Zhou, Ting, Liu, Wen Ling L, Matsunami, Hiroaki
Publicado no Sci Data (2015)

Mesothelin expression is associated with poor outcomes in breast cancer

Por Li, Yun R., Xian, Rena R., Ziober, Amy, Conejo-Garcia, Jose, Perales-Puchalt, Alfredo, June, Carl H., Zhang, Paul J., Tchou, Julia
Publicado no Breast Cancer Res Treat (2014)

A Novel Prospective Study Assessing the Combination of Photodynamic Therapy and Proton Radiation Therapy: Safety and Outcomes When Treating Malignant Pleural Mesothelioma

Por Rice, Stephanie R., Li, Yun R., Busch, Theresa M., Kim, Michele M., McNulty, Sally, Dimofte, Andrea, Zhu, Timothy C., Cengel, Keith A., Simone, Charles B.
Publicado no Photochem Photobiol (2018)

Genomic risk scores for juvenile idiopathic arthritis and its subtypes

Por Cánovas, Rodrigo, Cobb, Joanna, Brozynska, Marta, Bowes, John, Li, Yun R, Smith, Samantha Louise, Hakonarson, Hakon, Thomson, Wendy, Ellis, Justine A, Abraham, Gad, Munro, Jane E, Inouye, Michael
Publicado no Ann Rheum Dis (2020)

Uncovering the immune tumor microenvironment in non-small cell lung cancer to understand response rates to checkpoint blockade and radiation

Por Schoenhals, Jonathan E., Seyedin, Steven N., Anderson, Clark, Brooks, Eric D., Li, Yun R., Younes, Ahmed I., Niknam, Sharareh, Li, Ailin, Barsoumian, Hampartsoum B., Cortez, Maria Angelica, Welsh, James W.
Publicado no Transl Lung Cancer Res (2017)

Ataxin-2 intermediate-length polyglutamine expansions in European ALS patients

Por Lee, Teresa, Li, Yun R., Ingre, Caroline, Weber, Markus, Grehl, Torsten, Gredal, Ole, de Carvalho, Mamede, Meyer, Thomas, Tysnes, Ole-Björn, Auburger, Georg, Gispert, Suzana, Bonini, Nancy M., Andersen, Peter M., Gitler, Aaron D.
Publicado em 2011

The Missense of Smell: Functional Variability in the Human Odorant Receptor Repertoire

Por Mainland, Joel D., Keller, Andreas, Li, Yun R., Zhou, Ting, Trimmer, Casey, Snyder, Lindsey L., Moberly, Andrew H., Adipietro, Kaylin A., Liu, Wen Ling L., Zhuang, Hanyi, Zhan, Senmiao, Lee, Somin S., Lin, Abigail, Matsunami, Hiroaki
Publicado em 2013

Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations

Por Cyrus, Cyril, Al-Mueilo, Samir, Vatte, Chittibabu, Chathoth, Shahanas, Li, Yun R., Qutub, Hatem, Al Ali, Rudaynah, Al-Muhanna, Fahad, Lanktree, Matthew B., Alkharsah, Khaled Riyad, Al-Rubaish, Abdullah, Kim-Mozeleski, Brian, Keating, Brendan, Al Ali, Amein
Publicado no BMC Nephrol (2018)

Fasoracetam in adolescents with ADHD and glutamatergic gene network variants disrupting mGluR neurotransmitter signaling

Por Elia, Josephine, Ungal, Grace, Kao, Charlly, Ambrosini, Alexander, De Jesus-Rosario, Nilsa, Larsen, Lene, Chiavacci, Rosetta, Wang, Tiancheng, Kurian, Christine, Titchen, Kanani, Sykes, Brian, Hwang, Sharon, Kumar, Bhumi, Potts, Jacqueline, Davis, Joshua, Malatack, Jeffrey, Slattery, Emma, Moorthy, Ganesh, Zuppa, Athena, Weller, Andrew, Byrne, Enda, Li, Yun R., Kraft, Walter K., Hakonarson, Hakon
Publicado no Nat Commun (2018)

Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array

Por Rodriguez, Santiago, Gaunt, Tom R, Guo, Yiran, Zheng, Jie, Barnes, Michael R, Tang, Weihang, Danish, Fazal, Johnson, Andrew, Castillo, Berta A, Li, Yun R, Hakonarson, Hakon, Buxbaum, Sarah G, Palmer, Tom, Tsai, Michael Y, Lange, Leslie A, Ebrahim, Shah, Davey Smith, George, Lawlor, Debbie A, Folsom, Aaron R, Hoogeveen, Ron, Reiner, Alex, Keating, Brendan, Day, Ian NM
Publicado no Eur J Hum Genet (2016)

A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

Por Li, Dong, Chang, Xiao, Connolly, John J., Tian, Lifeng, Liu, Yichuan, Bhoj, Elizabeth J., Robinson, Nora, Abrams, Debra, Li, Yun R., Bradfield, Jonathan P., Kim, Cecilia E., Li, Jin, Wang, Fengxiang, Snyder, James, Lemma, Maria, Hou, Cuiping, Wei, Zhi, Guo, Yiran, Qiu, Haijun, Mentch, Frank D., Thomas, Kelly A., Chiavacci, Rosetta M., Cone, Roger, Li, Bingshan, Sleiman, Patrick A., Hakonarson, Hakon
Publicado no Sci Rep (2017)

Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

Por Li, Dong, Chang, Xiao, Connolly, John J., Tian, Lifeng, Liu, Yichuan, Bhoj, Elizabeth J., Robinson, Nora, Abrams, Debra, Li, Yun R., Bradfield, Jonathan P., Kim, Cecilia E., Li, Jin, Wang, Fengxiang, Snyder, James, Lemma, Maria, Hou, Cuiping, Wei, Zhi, Guo, Yiran, Qiu, Haijun, Mentch, Frank D., Thomas, Kelly A., Chiavacci, Rosetta M., Cone, Roger, Li, Bingshan, Sleiman, Patrick A., Hakonarson, Hakon
Publicado no Sci Rep (2017)

Causal Effects of Body Mass Index on Cardiometabolic Traits and Events: A Mendelian Randomization Analysis

Por Holmes, Michael V., Lange, Leslie A., Palmer, Tom, Lanktree, Matthew B., North, Kari E., Almoguera, Berta, Buxbaum, Sarah, Chandrupatla, Hareesh R., Elbers, Clara C., Guo, Yiran, Hoogeveen, Ron C., Li, Jin, Li, Yun R., Swerdlow, Daniel I., Cushman, Mary, Price, Tom S., Curtis, Sean P., Fornage, Myriam, Hakonarson, Hakon, Patel, Sanjay R., Redline, Susan, Siscovick, David S., Tsai, Michael Y., Wilson, James G., van der Schouw, Yvonne T., FitzGerald, Garret A., Hingorani, Aroon D., Casas, Juan P., de Bakker, Paul I.W., Rich, Stephen S., Schadt, Eric E., Asselbergs, Folkert W., Reiner, Alex P., Keating, Brendan J.
Publicado em 2014

Causal Effects of Body Mass Index on Cardiometabolic Traits and Events: A Mendelian Randomization Analysis

Por Holmes, Michael V., Lange, Leslie A., Palmer, Tom, Lanktree, Matthew B., North, Kari E., Almoguera, Berta, Buxbaum, Sarah, Chandrupatla, Hareesh R., Elbers, Clara C., Guo, Yiran, Hoogeveen, Ron C., Li, Jin, Li, Yun R., Swerdlow, Daniel I., Cushman, Mary, Price, Tom S., Curtis, Sean P., Fornage, Myriam, Hakonarson, Hakon, Patel, Sanjay R., Redline, Susan, Siscovick, David S., Tsai, Michael Y., Wilson, James G., van der Schouw, Yvonne T., FitzGerald, Garret A., Hingorani, Aroon D., Casas, Juan P., de Bakker, Paul I.W., Rich, Stephen S., Schadt, Eric E., Asselbergs, Folkert W., Reiner, Alex P., Keating, Brendan J.
Publicado em 2014

Prion-like domain mutations in hnRNPs cause multisystem proteinopathy and ALS

Por Kim, Hong Joo, Kim, Nam Chul, Wang, Yong-Dong, Scarborough, Emily A., Moore, Jennifer, Diaz, Zamia, MacLea, Kyle S., Freibaum, Brian, Li, Songqing, Molliex, Amandine, Kanagaraj, Anderson P., Carter, Robert, Boylan, Kevin B., Wojtas, Aleksandra M., Rademakers, Rosa, Pinkus, Jack L., Greenberg, Steven A., Trojanowski, John Q., Traynor, Bryan J., Smith, Bradley N., Topp, Simon, Gkazi, Athina-Soragia, Miller, Jack, Shaw, Christopher E., Kottlors, Michael, Kirschner, Janbernd, Pestronk, Alan, Li, Yun R., Ford, Alice Flynn, Gitler, Aaron D., Benatar, Michael, King, Oliver D., Kimonis, Virginia E., Ross, Eric D., Weihl, Conrad C., Shorter, James, Taylor, J. Paul
Publicado em 2013

Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies

Por Li, Yun R., van Setten, Jessica, Verma, Shefali S., Lu, Yontao, Holmes, Michael V., Gao, Hui, Lek, Monkol, Nair, Nikhil, Chandrupatla, Hareesh, Chang, Baoli, Karczewski, Konrad J., Wong, Chanel, Mohebnasab, Maede, Mukhtar, Eyas, Phillips, Randy, Tragante, Vinicius, Hou, Cuiping, Steel, Laura, Lee, Takesha, Garifallou, James, Guettouche, Toumy, Cao, Hongzhi, Guan, Weihua, Himes, Aubree, van Houten, Jacob, Pasquier, Andrew, Yu, Reina, Carrigan, Elena, Miller, Michael B., Schladt, David, Akdere, Abdullah, Gonzalez, Ana, Llyod, Kelsey M., McGinn, Daniel, Gangasani, Abhinav, Michaud, Zach, Colasacco, Abigail, Snyder, James, Thomas, Kelly, Wang, Tiancheng, Wu, Baolin, Alzahrani, Alhusain J., Al-Ali, Amein K., Al-Muhanna, Fahad A., Al-Rubaish, Abdullah M., Al-Mueilo, Samir, Monos, Dimitri S., Murphy, Barbara, Olthoff, Kim M., Wijmenga, Cisca, Webster, Teresa, Kamoun, Malek, Balasubramanian, Suganthi, Lanktree, Matthew B., Oetting, William S., Garcia-Pavia, Pablo, MacArthur, Daniel G., de Bakker, Paul I W, Hakonarson, Hakon, Birdwell, Kelly A., Jacobson, Pamala A., Ritchie, Marylyn D., Asselbergs, Folkert W., Israni, Ajay K., Shaked, Abraham, Keating, Brendan J.
Publicado no Genome Med (2015)

Genetic sharing and heritability of paediatric age of onset autoimmune diseases

Por Li, Yun R., Zhao, Sihai D., Li, Jin, Bradfield, Jonathan P., Mohebnasab, Maede, Steel, Laura, Kobie, Julie, Abrams, Debra J., Mentch, Frank D., Glessner, Joseph T., Guo, Yiran, Wei, Zhi, Connolly, John J., Cardinale, Christopher J., Bakay, Marina, Li, Dong, Maggadottir, S. Melkorka, Thomas, Kelly A., Qui, Haijun, Chiavacci, Rosetta M., Kim, Cecilia E., Wang, Fengxiang, Snyder, James, Flatø, Berit, Førre, Øystein, Denson, Lee A., Thompson, Susan D., Becker, Mara L., Guthery, Stephen L., Latiano, Anna, Perez, Elena, Resnick, Elena, Strisciuglio, Caterina, Staiano, Annamaria, Miele, Erasmo, Silverberg, Mark S., Lie, Benedicte A., Punaro, Marilynn, Russell, Richard K., Wilson, David C., Dubinsky, Marla C., Monos, Dimitri S., Annese, Vito, Munro, Jane E., Wise, Carol, Chapel, Helen, Cunningham-Rundles, Charlotte, Orange, Jordan S., Behrens, Edward M., Sullivan, Kathleen E., Kugathasan, Subra, Griffiths, Anne M., Satsangi, Jack, Grant, Struan F. A., Sleiman, Patrick M. A., Finkel, Terri H., Polychronakos, Constantin, Baldassano, Robert N., Luning Prak, Eline T., Ellis, Justine A., Li, Hongzhe, Keating, Brendan J., Hakonarson, Hakon
Publicado no Nat Commun (2015)