Transcription factor regulation of eQTL activity across individuals and tissues von Flynn, Elise D, Tsu, Athena L, Kasela, Silva, Kim-Hellmuth, Sarah, Aguet, Francois, Ardlie, Kristin G, Bussemaker, Harmen J, Mohammadi, Pejman, Lappalainen, Tuuli

Volltext

Functional Characterization of Genetic Variant Effects on Expression von Flynn, Elise D, Lappalainen, Tuuli

Volltext

Modeling RNA-Binding Protein Specificity In Vivo by Precisely Registering Protein-RNA Crosslink Sites von Feng, Huijuan, Bao, Suying, Rahman, Mohammad Alinoor, Weyn-Vanhentenryck, Sebastien M., Khan, Aziz, Wong, Justin, Shah, Ankeeta, Flynn, Elise D., Krainer, Adrian R., Zhang, Chaolin

Volltext

Distinct epigenomic patterns are associated with haploinsufficiency and predict risk genes of developmental disorders von Han, Xinwei, Chen, Siying, Flynn, Elise, Wu, Shuang, Wintner, Dana, Shen, Yufeng

Volltext

Kawasaki Disease Shock Syndrome with Retrograde Diastolic Aortic Flow von Flynn, Elise, MBBS, BMedSci, Kowalski, Remi, MBBS (Hons), FRACP, Burgner, David, MBChB, FRACP, PhD

Volltext

Defining Disease, Diagnosis, and Translational Medicine within a Homeostatic Perturbation Paradigm: The National Institutes of Health Undiagnosed Diseases Program Experience von Gall, Timothy, Valkanas, Elise, Bello, Christofer, Markello, Thomas, Adams, Christopher, Bone, William P, Brandt, Alexander J, Brazill, Jennifer M, Carmichael, Lynn, Davids, Mariska, Davis, Joie, Diaz-Perez, Zoraida, Draper, David, Elson, Jeremy, Flynn, Elise D, Godfrey, Rena, Groden, Catherine, Hsieh, Cheng-Kang, Fischer, Roxanne, Golas, Gretchen A, Guzman, Jessica, Huang, Yan, Kane, Megan S, Lee, Elizabeth, Li, Chong, Links, Amanda E, Maduro, Valerie, Malicdan, May Christine V, Malik, Fayeza S, Nehrebecky, Michele, Park, Joun, Pemberton, Paul, Schaffer, Katherine, Simeonov, Dimitre, Sincan, Murat, Smedley, Damian, Valivullah, Zaheer, Wahl, Colleen, Washington, Nicole, Wolfe, Lynne A, Xu, Karen, Zhu, Yi, Gahl, William A, Tifft, Cynthia J, Toro, Camillo, Adams, David R, He, Miao, Robinson, Peter N, Haendel, Melissa A, Zhai, R Grace, Boerkoel, Cornelius F

Volltext

Utilising genexpert to identify cml in the primary care setting: triggers for testing and predictors of positive results von Flynn, Elise, Maxwell, Ellen

Volltext

Bowel perforation complicating an ACTH-secreting phaeochromocytoma von Flynn, Elise, Baqar, Sara, Liu, Dorothy, Ekinci, Elif I, Farrell, Stephen, Zajac, Jeffrey D, De Luise, Mario, Seeman, Ego

Volltext

The GTEx Consortium atlas of genetic regulatory effects across human tissues von Aguet, Francois, Barbeira, Alvaro N., Bonazzola, Rodrigo, Brown, Andrew, Castel, Stephane E., Jo, Brian, Kasela, Silva, Kim-Hellmuth, Sarah, Liang, Yanyu, Parsana, Princy, Flynn, Elise, Fresard, Laure, Gamazon, Eric R., Hamel, Andrew R., He, Yuan, Hormozdiari, Farhad, Mohammadi, Pejman, Munoz-Aguirre, Manuel, Ardlie, Kristin G., Battle, Alexis, Bonazzola, Rodrigo, Brown, Christopher D., Cox, Nancy, Dermitzakis, Emmanouil T., Engelhardt, Barbara E., Garrido-Martin, Diego, Gay, Nicole R., Getz, Gad, Guigo, Roderic, Hamel, Andrew R., Handsaker, Robert E., He, Yuan, Hoffman, Paul J., Hormozdiari, Farhad, Im, Hae Kyung, Jo, Brian, Kasela, Silva, Kashin, Seva, Kim-Hellmuth, Sarah, Kwong, Alan, Lappalainen, Tuuli, Li, Xiao, Liang, Yanyu, MacArthur, Daniel G., Mohammadi, Pejman, Montgomery, Stephen B., Munoz-Aguirre, Manuel, Rouhana, John M., Hormozdiari, Farhad, Im, Hae Kyung, Kim-Hellmuth, Sarah, Ardlie, Kristin G., Getz, Gad, Guigo, Roderic, Im, Hae Kyung, Lappalainen, Tuuli, Montgomery, Stephen B., Im, Hae Kyung, Lappalainen, Tuuli, Lappalainen, Tuuli, Anand, Shankara, Gabriel, Stacey, Getz, Gad, Graubert, Aaron, Hadley, Kane, Handsaker, Robert E., Huang, Katherine H., Kashin, Seva, Li, Xiao, MacArthur, Daniel G., Meier, Samuel R., Nedzel, Jared L., Balliu, Brunilda, Conrad, Don, Cotter, Daniel J., Das, Sayantan, de Goede, Olivia M., Eskin, Eleazar, Eulalio, Tiffany Y., Ferraro, Nicole M., Garrido-Martin, Diego, Gay, Nicole R., Getz, Gad, Graubert, Aaron, Guigo, Roderic, Hadley, Kane, Hamel, Andrew R., Handsaker, Robert E., He, Yuan, Hoffman, Paul J., Hormozdiari, Farhad, Hou, Lei, Huang, Katherine H., Im, Hae Kyung, Jo, Brian, Kasela, Silva, Kashin, Seva, Kellis, Manolis, Kim-Hellmuth, Sarah, Kwong, Alan

Volltext

The impact of sex on gene expression across human tissues von Oliva, Meritxell, Munoz-Aguirre, Manuel, Kim-Hellmuth, Sarah, Wucher, Valentin, Gewirtz, Ariel D. H., Cotter, Daniel J., Parsana, Princy, Kasela, Silva, Balliu, Brunilda, Vinuela, Ana, Castel, Stephane E., Mohammadi, Pejman, Aguet, Francois, Zou, Yuxin, Khramtsova, Ekaterina A., Skol, Andrew D., Garrido-Martin, Diego, Reverter, Ferran, Brown, Andrew, Evans, Patrick, Gamazon, Eric R., Payne, Anthony, Bonazzola, Rodrigo, Barbeira, Alvaro N., Hamel, Andrew R., Martinez-Perez, Angel, Soria, Jose Manuel, Pierce, Brandon L., Stephens, Matthew, Eskin, Eleazar, Dermitzakis, Emmanouil T., Segr, Ayellet, Im, Hae Kyung, Engelhardt, Barbara E., Ardlie, Kristin G., Montgomery, Stephen B., Battle, Alexis J., Lappalainen, Tuuli, Guigo, Roderic, Stranger, Barbara E.

Volltext

Determinants of telomere length across human tissues von Demanelis, Kathryn, Jasmine, Farzana, Chen, Lin S., Chernoff, Meytal, Tong, Lin, Delgado, Dayana, Zhang, Chenan, Shinkle, Justin, Sabarinathan, Mekala, Lin, Hannah, Ramirez, Eduardo, Oliva, Meritxell, Kim-Hellmuth, Sarah, Stranger, Barbara E., Lai, Tsung-Po, Aviv, Abraham, Ardlie, Kristin G., Aguet, Francois, Ahsan, Habibul, Doherty, Jennifer A., Kibriya, Muhammad G., Pierce, Brandon L.

Volltext

A Quantitative Proteome Map of the Human Body von Jiang, Lihua, Chan, Joanne, Fang, Huaying, Anand, Shankara, Gabriel, Stacey, Graubert, Aaron, Hadley, Kane, Huang, Katherine H., MacArthur, Daniel G., Meier, Samuel R., Segrè, Ayellet V., Balliu, Brunilda, Barbeira, Alvaro N., Battle, Alexis, Brown, Andrew, Brown, Christopher D., Castel, Stephane E., Conrad, Don, Cotter, Daniel J., Das, Sayantan, de Goede, Olivia M., Dermitzakis, Emmanouil T., Eskin, Eleazar, Eulalio, Tiffany Y., Garrido-Martín, Diego, Guigó, Roderic, He, Yuan, Hoffman, Paul J., Hormozdiari, Farhad, Im, Hae Kyung, Jo, Brian, Kasela, Silva, Kellis, Manolis, Kim-Hellmuth, Sarah, Li, Xin, Mohammadi, Pejman, Montgomery, Stephen B., Muñoz-Aguirre, Manuel, Nachun, Daniel C., Oliva, Meritxell, Parsana, Princy, Sabatti, Chiara, Skol, Andrew D., Stephens, Matthew, Strober, Benjamin J., Teran, Nicole A., Viñuela, Ana, Wang, Gao, Wucher, Valentin, Zou, Yuxin, Ferreira, Pedro G., Yeger-Lotem, Esti, Barcus, Mary E., Bradbury, Debra, Krubit, Tanya, McLean, Jeffrey A., Smith, Anna M., Sobin, Leslie, Tabor, David E., Brigham, Lori E., Gillard, Bryan M., Hasz, Richard, Johnson, Mark, Kopen, Gene, Moser, Michael T., Myer, Kevin, Shad, Saboor, Thomas, Jeffrey A., Washington, Michael, Rohrer, Daniel C., Valley, Dana R., Davis, David A., Mash, Deborah C., Mosavel, Maghboeba, Siminoff, Laura A., Flicek, Paul, Juettemann, Thomas, Powell, Conner C., Rosenbloom, Kate R., Ruffier, Magali, Sheppard, Dan, Taylor, Kieron, Akey, Joshua, Demanelis, Kathryn, Feinberg, Andrew P., Hansen, Kasper D., Kibriya, Muhammad G., Li, Jin Billy, Li, Qin, Linder, Sandra E., Pierce, Brandon L., Smith, Kevin S., Tang, Hua, Carithers, Latarsha J., Koester, Susan E., Little, A. Roger, Moore, Helen M., Rao, Abhi K., Vaught, Jimmie B., Volpi, Simona

Volltext

Cell type-specific genetic regulation of gene expression across human tissues von Kim-Hellmuth, Sarah, Aguet, Francois, Oliva, Meritxell, Munoz-Aguirre, Manuel, Wucher, Valentin, Kasela, Silva, Castel, Stephane E., Hamel, Andrew R., Vinuela, Ana, Roberts, Amy L., Mangul, Serghei, Wen, Xiaoquan, Wang, Gao, Barbeira, Alvaro N., Garrido-Martin, Diego, Nadel, Brian, Zou, Yuxin, Bonazzola, Rodrigo, Quan, Jie, Brown, Andrew, Martinez-Perez, Angel, Soria, Jose Manuel, Getz, Gad, Dermitzakis, Emmanouil T., Small, Kerrin S., Stephens, Matthew, Xi, Hualin S., Im, Hae Kyung, Guig, Roderic, Segr, Ayellet, Stranger, Barbara E., Ardlie, Kristin G., Lappalainen, Tuuli

Volltext

Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease von Gloudemans, Michael J., Smail, Craig, Eulalio, Tiffany Y., Aguet, François, Xu, Jishu, Kim-Hellmuth, Sarah, Park, YoSon, Scott, Alexandra J., Strober, Benjamin J., Gabriel, Stacey, Meier, Samuel R., Nguyen, Duyen T., Segrè, Ayellet V., Brown, Andrew, Cotter, Daniel J., Cox, Nancy, Dermitzakis, Emmanouil T., Einson, Jonah, Flynn, Elise D., Fresard, Laure, Gamazon, Eric R., Gay, Nicole R., Guigó, Roderic, Hamel, Andrew R., He, Yuan, Hoffman, Paul J., Hormozdiari, Farhad, Hou, Lei, Jo, Brian, Kashin, Seva, Mohammadi, Pejman, Oliva, Meritxell, Parsana, Princy, Sabatti, Chiara, Stranger, Barbara E., Teran, Nicole A., Viñuela, Ana, Wang, Gao, Wright, Fred, Ferreira, Pedro G., Li, Gen, Yeger-Lotem, Esti, Bradbury, Debra, Qi, Liqun, Robinson, Karna, Roche, Nancy V., Tabor, David E., Bridge, Jason, Gillard, Bryan M., Hasz, Richard, Hunter, Marcus, Kopen, Gene, Leinweber, William F., Moser, Michael T., Myer, Kevin, Washington, Michael, Wheeler, Joseph, Rohrer, Daniel C., Valley, Dana R., Branton, Philip A., Sobin, Leslie, Gardiner, Heather M., Mosavel, Maghboeba, Siminoff, Laura A., Flicek, Paul, Haeussler, Maximilian, Juettemann, Thomas, Ruffier, Magali, Sheppard, Dan, Taylor, Kieron, Abell, Nathan S., Akey, Joshua, Chen, Lin, Feinberg, Andrew P., Hansen, Kasper D., Jasmine, Farzana, Jiang, Lihua, Kaul, Rajinder, Kibriya, Muhammad G., Li, Jin Billy, Li, Qin, Lin, Shin, Pierce, Brandon L., Skol, Andrew D., Smith, Kevin S., Snyder, Michael, Stamatoyannopoulos, John, Tang, Hua, Guan, Ping, Little, A. Roger, Nierras, Concepcion R., Rao, Abhi K., Volpi, Simona, Brown, Christopher D., Wen, Xiaoquan, Hall, Ira M., Lappalainen, Tuuli, Im, Hae Kyung, Quertermous, Thomas, Kirkegaard, Karla

Volltext

Transcriptomic signatures across human tissues identify functional rare genetic variation von Ferraro, Nicole M., Strober, Benjamin J., Einson, Jonah, Abell, Nathan S., Aguet, Francois, Barbeira, Alvaro N., Brandt, Margot, Bucan, Maja, Castel, Stephane E., Davis, Joe R., Greenwald, Emily, Hess, Gaelen T., Hilliard, Austin T., Kember, Rachel L., Kotis, Bence, Park, YoSon, Peloso, Gina, Ramdas, Shweta, Scott, Alexandra J., Smail, Craig, Tsang, Emily K., Zekavat, Seyedeh M., Ziosi, Marcello, Aradhana, Ardlie, Kristin G., Assimes, Themistocles L., Bassik, Michael C., Brown, Christopher D., Correa, Adolfo, Hall, Ira, Im, Hae Kyung, Li, Xin, Natarajan, Pradeep, Lappalainen, Tuuli, Mohammadi, Pejman, Montgomery, Stephen B., Battlett, Alexis

Volltext

Antithrombotic management and thrombosis rates in children post–liver transplantation: A case series and literature review von Flynn, Elise, Huang, Joanna Y., Hardikar, Winita, Herd, Lauren, Hodgson, Alexandra, Monagle, Paul

Volltext

A vast resource of allelic expression data spanning human tissues von Castel, Stephane E., Aguet, Francois, Mohammadi, Pejman, Ardlie, Kristin G., Lappalainen, Tuuli

Volltext

Abstract 10865: Elucidating the Variant-to-Function Relationship for LIPA, a Risk Locus of Coronary Artery Diseases von Li, Fang, Flynn, Elise, Xue, Chenyi, Meng, Yujiao, Wang, Ziyi, Wu, Xun, Li, Sufang, Cui, Jian, Shi, Jianting, Chirikjian, Margot K., Zhu, Yizhou, Rozenblyum, Annie, Shan, Sophie, Razani, Babak, Westerterp, Marit, Bauer, Robert, Jin, Fulai, Suh, Yousin, Lappalainen, Tuuli, Zhang, Hanrui

Volltext

Pharmacogenomic incidental findings in 308 families: The NIH Undiagnosed Diseases Program experience von Lee, Elizabeth M.J., Xu, Karen, Mosbrook, Emma, Links, Amanda, Guzman, Jessica, Adams, David R., Flynn, Elise, Valkanas, Elise, Toro, Camillo, Tifft, Cynthia J., Boerkoel, Cornelius F., Gahl, William A., Sincan, Murat

Volltext

Phenotypic evolution of UNC80 loss of function von Valkanas, Elise, Schaffer, Katherine, Dunham, Christopher, Maduro, Valerie, du Souich, Christèle, Rupps, Rosemarie, Adams, David R., Baradaran-Heravi, Alireza, Flynn, Elise, Malicdan, May C., Gahl, William A., Toro, Camilo, Boerkoel, Cornelius F.

Volltext