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

von Li, Yun R, Keating, Brendan J
Veröffentlicht in Genome Med (2014)

Stress granules as crucibles of ALS pathogenesis

von Li, Yun R., King, Oliver D., Shorter, James, Gitler, Aaron D.
Veröffentlicht 2013

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

von Li, Yun R, Levine, John E, Hakonarson, Hakon, Keating, Brendan J
Veröffentlicht 2014

Human olfactory receptor responses to odorants

von Mainland, Joel D, Li, Yun R, Zhou, Ting, Liu, Wen Ling L, Matsunami, Hiroaki
Veröffentlicht in Sci Data (2015)

Mesothelin expression is associated with poor outcomes in breast cancer

von Li, Yun R., Xian, Rena R., Ziober, Amy, Conejo-Garcia, Jose, Perales-Puchalt, Alfredo, June, Carl H., Zhang, Paul J., Tchou, Julia
Veröffentlicht in 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

von 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.
Veröffentlicht in Photochem Photobiol (2018)

Genomic risk scores for juvenile idiopathic arthritis and its subtypes

von 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
Veröffentlicht in Ann Rheum Dis (2020)

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

von 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.
Veröffentlicht in Transl Lung Cancer Res (2017)

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

von 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.
Veröffentlicht 2011

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

von 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
Veröffentlicht 2013

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

von 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
Veröffentlicht in BMC Nephrol (2018)

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

von 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
Veröffentlicht in Nat Commun (2018)

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

von 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
Veröffentlicht in Eur J Hum Genet (2016)

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

von 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
Veröffentlicht in Sci Rep (2017)

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

von 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
Veröffentlicht in Sci Rep (2017)

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

von 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.
Veröffentlicht 2014

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

von 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.
Veröffentlicht 2014

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

von 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
Veröffentlicht 2013

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

von 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.
Veröffentlicht in Genome Med (2015)

Genetic sharing and heritability of paediatric age of onset autoimmune diseases

von 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
Veröffentlicht in Nat Commun (2015)