Interaction induced Raman light scattering as a probe of the local density structure of binary supercritical solutions von BAGLIN, FRANK G., MURRAY, SUSAN K., DAUGHERTY, JILL E., PALMER, TASHA E., STANBERY, WAYNE

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Genome‐Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium von Young, Kendra A., Palmer, Nicholette D., Fingerlin, Tasha E., Langefeld, Carl D., Norris, Jill M., Wang, Nan, Xiang, Anny H., Guo, Xiuqing, Williams, Adrienne H., Chen, Yii‐Der I., Taylor, Kent D., Rotter, Jerome I., Raffel, Leslie J., Goodarzi, Mark O., Watanabe, Richard M., Wagenknecht, Lynne E.

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Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics)... von Palmer, Nicholette D, Goodarzi, Mark O, Langefeld, Carl D, Wang, Nan, Guo, Xiuqing, Taylor, Kent D, Fingerlin, Tasha E, Norris, Jill M, Buchanan, Thomas A, Xiang, Anny H, Haritunians, Talin, Ziegler, Julie T, Williams, Adrienne H, Stefanovski, Darko, Cui, Jinrui, Mackay, Adrienne W, Henkin, Leora F, Bergman, Richard N, Gao, Xiaoyi, Gauderman, James, Varma, Rohit, Hanis, Craig L, Cox, Nancy J, Highland, Heather M, Below, Jennifer E, Williams, Amy L, Burtt, Noel P, Aguilar-Salinas, Carlos A, Huerta-Chagoya, Alicia, Gonzalez-Villalpando, Clicerio, Orozco, Lorena, Haiman, Christopher A, Tsai, Michael Y, Johnson, W Craig, Yao, Jie, Rasmussen-Torvik, Laura, Pankow, James, Snively, Beverly, Jackson, Rebecca D, Liu, Simin, Nadler, Jerry L, Kandeel, Fouad, Chen, Yii-Der I, Bowden, Donald W, Rich, Stephen S, Raffel, Leslie J, Rotter, Jerome I, Watanabe, Richard M, Wagenknecht, Lynne E

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Transcriptional Adaptation of Drug-tolerant Mycobacterium tuberculosis During Treatment of Human Tuberculosis von Walter, Nicholas D., Dolganov, Gregory M., Garcia, Benjamin J., Worodria, William, Andama, Alfred, Musisi, Emmanuel, Ayakaka, Irene, Van, Tran T., Voskuil, Martin I., de Jong, Bouke C., Davidson, Rebecca M., Fingerlin, Tasha E., Kechris, Katerina, Palmer, Claire, Nahid, Payam, Daley, Charles L., Geraci, Mark, Huang, Laurence, Cattamanchi, Adithya, Strong, Michael, Schoolnik, Gary K., Davis, John Lucian

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Deep-coverage whole genome sequences and blood lipids among 16,324 individuals von Natarajan, Pradeep, Peloso, Gina M., Zekavat, Seyedeh Maryam, Montasser, May, Ganna, Andrea, Chaffin, Mark, Khera, Amit V., Zhou, Wei, Bloom, Jonathan M., Engreitz, Jesse M., Ernst, Jason, O’Connell, Jeffrey R., Ruotsalainen, Sanni E., Alver, Maris, Manichaikul, Ani, Johnson, W. Craig, Perry, James A., Poterba, Timothy, Seed, Cotton, Surakka, Ida L., Esko, Tonu, Ripatti, Samuli, Salomaa, Veikko, Correa, Adolfo, Vasan, Ramachandran S., Kellis, Manolis, Neale, Benjamin M., Lander, Eric S., Abecasis, Goncalo, Mitchell, Braxton, Rich, Stephen S., Wilson, James G., Cupples, L. Adrienne, Rotter, Jerome I., Willer, Cristen J., Kathiresan, Sekar

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A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies von Li, Zilin, Li, Xihao, Zhou, Hufeng, Gaynor, Sheila M., Selvaraj, Margaret Sunitha, Arapoglou, Theodore, Quick, Corbin, Liu, Yaowu, Chen, Han, Sun, Ryan, Dey, Rounak, Arnett, Donna K., Auer, Paul L., Bielak, Lawrence F., Bis, Joshua C., Blackwell, Thomas W., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Brody, Jennifer A., Cade, Brian E., Conomos, Matthew P., Correa, Adolfo, Cupples, L. Adrienne, Curran, Joanne E., de Vries, Paul S., Duggirala, Ravindranath, Franceschini, Nora, Freedman, Barry I., Göring, Harald H. H., Guo, Xiuqing, Kalyani, Rita R., Kooperberg, Charles, Kral, Brian G., Lange, Leslie A., Lin, Bridget M., Manichaikul, Ani, Manning, Alisa K., Martin, Lisa W., Mathias, Rasika A., Meigs, James B., Mitchell, Braxton D., Montasser, May E., Morrison, Alanna C., Naseri, Take, O’Connell, Jeffrey R., Palmer, Nicholette D., Peyser, Patricia A., Psaty, Bruce M., Raffield, Laura M., Redline, Susan, Reiner, Alexander P., Reupena, Muagututi’a Sefuiva, Rice, Kenneth M., Rich, Stephen S., Smith, Jennifer A., Taylor, Kent D., Taub, Margaret A., Vasan, Ramachandran S., Weeks, Daniel E., Wilson, James G., Yanek, Lisa R., Zhao, Wei, Rotter, Jerome I., Willer, Cristen J., Natarajan, Pradeep, Peloso, Gina M., Lin, Xihong

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Whole genome sequence analysis of blood lipid levels in >66,000 individuals von Selvaraj, Margaret Sunitha, Li, Xihao, Li, Zilin, Pampana, Akhil, Zhang, David Y., Park, Joseph, Aslibekyan, Stella, Bis, Joshua C., Brody, Jennifer A., Cade, Brian E., Chuang, Lee-Ming, Chung, Ren-Hua, Curran, Joanne E., de las Fuentes, Lisa, de Vries, Paul S., Duggirala, Ravindranath, Freedman, Barry I., Graff, Mariaelisa, Guo, Xiuqing, Heard-Costa, Nancy, Hidalgo, Bertha, Hwu, Chii-Min, Irvin, Marguerite R., Kelly, Tanika N., Kral, Brian G., Lange, Leslie, Li, Xiaohui, Lisa, Martin, Lubitz, Steven A., Manichaikul, Ani W., Michael, Preuss, Montasser, May E., Morrison, Alanna C., Naseri, Take, O’Connell, Jeffrey R., Palmer, Nicholette D., Peyser, Patricia A., Reupena, Muagututia S., Smith, Jennifer A., Sun, Xiao, Taylor, Kent D., Tracy, Russell P., Tsai, Michael Y., Wang, Zhe, Wang, Yuxuan, Bao, Wei, Wilkins, John T., Yanek, Lisa R., Zhao, Wei, Arnett, Donna K., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Chen, Yii-Der Ida, Correa, Adolfo, Cupples, L. Adrienne, Dutcher, Susan K., Ellinor, Patrick T., Fornage, Myriam, Gabriel, Stacey, Germer, Soren, Gibbs, Richard, He, Jiang, Kaplan, Robert C., Kardia, Sharon L. R., Kim, Ryan, Kooperberg, Charles, Loos, Ruth J. F., Viaud-Martinez, Karine A, Mathias, Rasika A., McGarvey, Stephen T., Mitchell, Braxton D., Nickerson, Deborah, North, Kari E., Psaty, Bruce M., Redline, Susan, Reiner, Alexander P., Vasan, Ramachandran S., Rich, Stephen S., Willer, Cristen, Rotter, Jerome I., Rader, Daniel J., Lin, Xihong, Peloso, Gina M., Natarajan, Pradeep

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Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries von Zekavat, Seyedeh M., Ruotsalainen, Sanni, Handsaker, Robert E., Alver, Maris, Bloom, Jonathan, Poterba, Timothy, Seed, Cotton, Ernst, Jason, Chaffin, Mark, Engreitz, Jesse, Peloso, Gina M., Manichaikul, Ani, Yang, Chaojie, Ryan, Kathleen A., Fu, Mao, Johnson, W. Craig, Tsai, Michael, Budoff, Matthew, Vasan, Ramachandran S., Cupples, L. Adrienne, Rotter, Jerome I., Rich, Stephen S., Post, Wendy, Mitchell, Braxton D., Correa, Adolfo, Metspalu, Andres, Wilson, James G., Salomaa, Veikko, Kellis, Manolis, Daly, Mark J., Neale, Benjamin M., McCarroll, Steven, Surakka, Ida, Esko, Tonu, Ganna, Andrea, Ripatti, Samuli, Kathiresan, Sekar, Natarajan, Pradeep

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Differential associations of neighborhood disadvantage, race/ethnicity, and cognitive status with experiences of psychosocial distress in the HABS-HD cohort von Rhoads, Tasha, Wong, Christina G, Cobos, Kimberly, O'Bryant, Sid E, Kind, Amy J H, Miller, Justin B

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Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes von Weinstock, Joshua S., Nandakumar, Satish K., Bao, Erik L., Szeto, Mindy D., Liao, Xiaotian, Nasser, Joseph, Laurie, Cecelia, Burugula, Bala Bharathi, Gibson, Christopher J., Lin, Amy E., Aguet, Francois, Ardlie, Kristin, Mitchell, Braxton D., Barnes, Kathleen C., Moscati, Arden, Redline, Susan, Psaty, Bruce M., Silverman, Edwin K., Weiss, Scott T., Palmer, Nicholette D., Vasan, Ramachandran S., He, Jiang, Kaplan, Robert C., Smith, Nicholas L., Arnett, Donna K., Schwartz, David A., Guo, Xiuqing, Konkle, Barbara A., Custer, Brian, Peralta, Juan M., Gui, Hongsheng, Meyers, Deborah A., McGarvey, Stephen T., Chen, Ida Yii-Der, Shoemaker, M. Benjamin, Peyser, Patricia A., Broome, Jai G., Wang, Fei Fei, North, Kari E., Launer, Lenore J., Cade, Brian E., Bis, Joshua C., Cho, Michael H., Lasky-Su, Jessica, Bowden, Donald W., Cupples, L. Adrienne, Mak, Angel C. Y., Smith, Jennifer A., Kelly, Tanika N., Aslibekyan, Stella, Heckbert, Susan R., Tiwari, Hemant K., Yang, Ivana V., Heit, John A., Johnsen, Jill M., Curran, Joanne E., Wenzel, Sally E., Rao, Dabeeru C., Darbar, Dawood, Moon, Jee-Young, Tracy, Russell P., Buth, Erin J., Rafaels, Nicholas, Loos, Ruth J. F., Liu, Yongmei, Hou, Lifang, Lee, Jiwon, Kachroo, Priyadarshini, Freedman, Barry I., Levy, Daniel, Bielak, Lawrence F., Hixson, James E., Floyd, James S., Whitsel, Eric A., Ellinor, Patrick T., Irvin, Marguerite R., Fingerlin, Tasha E., Armasu, Sebastian M., Wheeler, Marsha M., Blangero, John, Williams, L. Keoki, Levy, Bruce D., Sheu, Wayne Huey-Herng, Roden, Dan M., Boerwinkle, Eric, Taylor, Kent D., Johnson, Andrew D., Auer, Paul L., Kooperberg, Charles, Laurie, Cathy C., Blackwell, Thomas W., Smith, Albert V., Lange, Ethan, Rotter, Jerome I., Kitzman, Jacob O., Lander, Eric S., Ebert, Benjamin L., Reiner, Alexander P., Jaiswal, Siddhartha, Kathiresan, Sekar

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Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies von Li, Xihao, Quick, Corbin, Zhou, Hufeng, Gaynor, Sheila M., Liu, Yaowu, Chen, Han, Selvaraj, Margaret Sunitha, Sun, Ryan, Dey, Rounak, Arnett, Donna K., Bielak, Lawrence F., Bis, Joshua C., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Brody, Jennifer A., Cade, Brian E., Correa, Adolfo, Cupples, L. Adrienne, Curran, Joanne E., de Vries, Paul S., Duggirala, Ravindranath, Freedman, Barry I., Göring, Harald H. H., Guo, Xiuqing, Haessler, Jeffrey, Kalyani, Rita R., Kooperberg, Charles, Kral, Brian G., Lange, Leslie A., Manichaikul, Ani, Martin, Lisa W., McGarvey, Stephen T., Mitchell, Braxton D., Montasser, May E., Morrison, Alanna C., Naseri, Take, O’Connell, Jeffrey R., Palmer, Nicholette D., Peyser, Patricia A., Psaty, Bruce M., Raffield, Laura M., Redline, Susan, Reiner, Alexander P., Reupena, Muagututi’a Sefuiva, Rice, Kenneth M., Rich, Stephen S., Sitlani, Colleen M., Smith, Jennifer A., Taylor, Kent D., Vasan, Ramachandran S., Willer, Cristen J., Wilson, James G., Yanek, Lisa R., Zhao, Wei, Rotter, Jerome I., Natarajan, Pradeep, Peloso, Gina M., Li, Zilin, Lin, Xihong

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Genome-wide association study of vitamin D concentrations in Hispanic Americans: The IRAS Family Study von Engelman, Corinne D., Meyers, Kristin J., Ziegler, Julie T., Taylor, Kent D., Palmer, Nicholette D., Haffner, Steven M., Fingerlin, Tasha E., Wagenknecht, Lynne E., Rotter, Jerome I., Bowden, Donald W., Langefeld, Carl D., Norris, Jill M.

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Parent proxy–reported health‐related quality of life and fatigue in pediatric patients diagnosed with brain tumors and acute lymphoblastic leukemia von Meeske, Kathleen, Katz, Ernest R., Palmer, Stephanie N., Burwinkle, Tasha, Varni, James W.

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Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed von Keener, Rebecca, Iyer, Kruthika R., Weinstock, Joshua S., Lane, John, Miller-Fleming, Tyne W., Brody, Jennifer A., Raffield, Laura M., McHugh, Caitlin P., Jain, Deepti, Gogarten, Stephanie M., Laurie, Cecelia A., Keramati, Ali, Arvanitis, Marios, Smith, Albert V., Heavner, Benjamin, Bis, Joshua C., Blangero, John, Burchard, Esteban G., Celedón, Juan C., Chang, Yen Pei C., de las Fuentes, Lisa, DeMeo, Dawn L., Garrett, Melanie E., Hidalgo, Bertha A., Irvin, Marguerite R., Islam, Talat, Johnson, W. Craig, Kaab, Stefan, Launer, Lenore, Liu, Simin, Moscati, Arden, North, Kari E., Rafaels, Nicholas, Seidman, Christine, Weeks, Daniel E., Wen, Fayun, Wheeler, Marsha M., Williams, L. Keoki, Zhao, Wei, Aslibekyan, Stella, Auer, Paul L., Bowden, Donald W., Cade, Brian E., Cho, Michael H., Curran, Joanne E., Daya, Michelle, Deka, Ranjan, Eng, Celeste, Fingerlin, Tasha E., Guo, Xiuqing, Hou, Lifang, Johnsen, Jill M., Kenny, Eimear E., Liu, Chunyu, Minster, Ryan L., Nouraie, Mehdi, Smith, Jennifer A., Smith, Nicholas L., Lasky-Su, Jessica, Taylor, James G., Telen, Marilyn J., White, Marquitta J., Zhang, Yingze, Wiggins, Kerri L., Weiss, Scott T., Vasan, Ramachandran S., Taylor, Kent D., Sinner, Moritz F., Sheu, Wayne H.-H., Schwartz, David A., Raby, Benjamin A., Palmer, Nicholette D., Nekhai, Sergei, Montgomery, Courtney G., Mitchell, Braxton D., Meyers, Deborah A., Kumar, Rajesh, Konkle, Barbara A., Kelly, Shannon, Kaplan, Robert, He, Jiang, Gelb, Bruce D., Fornage, Myriam, Correa, Adolfo, Boerwinkle, Eric, Ashley-Koch, Allison E., Arnett, Donna K., Albert, Christine, Laurie, Cathy C., Abecasis, Goncalo, Nickerson, Deborah A., Wilson, James G., Levy, Daniel, Ruczinski, Ingo, Aviv, Abraham, Thornton, Timothy, O’Connell, Jeff, Armanios, Mary, Pankratz, Nathan, Mathias, Rasika A.

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Inherited Causes of Clonal Hematopoiesis in 97,691 TOPMed Whole Genomes von Bick, Alexander G., Weinstock, Joshua S., Nandakumar, Satish K., Fulco, Charles P., Bao, Erik L., Zekavat, Seyedeh M., Szeto, Mindy D., Liao, Xiaotian, Leventhal, Matthew J., Nasser, Joseph, Chang, Kyle, Laurie, Cecelia, Burugula, Bala Bharathi, Gibson, Christopher J., Lin, Amy E., Taub, Margaret A., Aguet, Francois, Ardlie, Kristin, Mitchell, Braxton D., Barnes, Kathleen C., Moscati, Arden, Fornage, Myriam, Redline, Susan, Psaty, Bruce M., Silverman, Edwin K., Weiss, Scott T., Palmer, Nicholette D., Vasan, Ramachandran S., Burchard, Esteban G., Kardia, Sharon L. R., He, Jiang, Kaplan, Robert C., Smith, Nicholas L., Arnett, Donna K., Schwartz, David A., Correa, Adolfo, de Andrade, Mariza, Guo, Xiuqing, Konkle, Barbara A., Custer, Brian, Peralta, Juan M., Gui, Hongsheng, Meyers, Deborah A., McGarvey, Stephen T., Chen, Ida Yii-Der, Shoemaker, M. Benjamin, Peyser, Patricia A., Broome, Jai G., Gogarten, Stephanie M., Wang, Fei Fei, Wong, Quenna, Montasser, May E., Daya, Michelle, Kenny, Eimear E., North, Kari E., Launer, Lenore J., Cade, Brian E., Bis, Joshua C., Cho, Michael H., Lasky-Su, Jessica, Bowden, Donald W., Cupples, L. Adrienne, Mak, Angel C., Becker, Lewis C., Smith, Jennifer A., Kelly, Tanika N., Aslibekyan, Stella, Heckbert, Susan R., Tiwari, Hemant K., Yang, Ivana V., Heit, John A., Lubitz, Steven, Johnsen, Jill M., Curran, Joanne E., Wenzel, Sally E., Weeks, Daniel E., Rao, Dabeeru C., Darbar, Dawood, Moon, Jee-Young, Tracy, Russell P., Buth, Erin J., Rafaels, Nicholas, Loos, Ruth J.F., Durda, Peter, Liu, Yongmei, Hou, Lifang, Lee, Jiwon, Kachroo, Priyadarshini, Freedman, Barry I., Levy, Daniel, Bielak, Lawrence F., Hixson, James E., Floyd, James S., Whitsel, Eric A., Ellinor, Patrick T., Irvin, Marguerite R., Fingerlin, Tasha E., Raffield, Laura M., Armasu, Sebastian M., Wheeler, Marsha M.

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Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program von Cade, Brian E, Lee, Jiwon, Sofer, Tamar, Wang, Heming, Zhang, Man, Chen, Han, Gharib, Sina A, Gottlieb, Daniel J, Guo, Xiuqing, Lane, Jacqueline M, Liang, Jingjing, Lin, Xihong, Mei, Hao, Patel, Sanjay R, Purcell, Shaun M, Saxena, Richa, Shah, Neomi A, Evans, Daniel S, Hanis, Craig L, Hillman, David R, Mukherjee, Sutapa, Palmer, Lyle J, Stone, Katie L, Tranah, Gregory J, Abecasis, Gonçalo R, Boerwinkle, Eric A, Correa, Adolfo, Cupples, L Adrienne, Kaplan, Robert C, Nickerson, Deborah A, North, Kari E, Psaty, Bruce M, Rotter, Jerome I, Rich, Stephen S, Tracy, Russell P, Vasan, Ramachandran S, Wilson, James G, Zhu, Xiaofeng, Redline, Susan

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Rare genetic variants explain missing heritability in smoking von Jang, Seon-Kyeong, Evans, Luke, Fialkowski, Allison, Arnett, Donna K., Ashley-Koch, Allison E., Barnes, Kathleen C., Becker, Diane M., Bis, Joshua C., Blangero, John, Bleecker, Eugene R., Boorgula, Meher Preethi, Bowden, Donald W., Brody, Jennifer A., Cade, Brian E., Jenkins, Brenda W. Campbell, Carson, April P., Chavan, Sameer, Cupples, L. Adrienne, Custer, Brian, Damrauer, Scott M., David, Sean P., de Andrade, Mariza, Dinardo, Carla L., Fingerlin, Tasha E., Fornage, Myriam, Freedman, Barry I., Garrett, Melanie E., Gharib, Sina A., Glahn, David C., Haessler, Jeffrey, Heckbert, Susan R., Hokanson, John E., Hou, Lifang, Hwang, Shih-Jen, Hyman, Matthew C., Judy, Renae, Justice, Anne E., Kaplan, Robert C., Kardia, Sharon L. R., Kelly, Shannon, Kim, Wonji, Kooperberg, Charles, Levy, Daniel, Lloyd-Jones, Donald M., Loos, Ruth J. F., Manichaikul, Ani W., Gladwin, Mark T., Martin, Lisa Warsinger, Nouraie, Mehdi, Melander, Olle, Meyers, Deborah A., Montgomery, Courtney G., North, Kari E., Oelsner, Elizabeth C., Palmer, Nicholette D., Payton, Marinelle, Peljto, Anna L., Peyser, Patricia A., Preuss, Michael, Psaty, Bruce M., Qiao, Dandi, Rader, Daniel J., Rafaels, Nicholas, Redline, Susan, Reed, Robert M., Reiner, Alexander P., Rich, Stephen S., Rotter, Jerome I., Schwartz, David A., Shadyab, Aladdin H., Silverman, Edwin K., Smith, Nicholas L., Smith, J. Gustav, Smith, Albert V., Smith, Jennifer A., Tang, Weihong, Taylor, Kent D., Telen, Marilyn J., Vasan, Ramachandran S., Gordeuk, Victor R., Wang, Zhe, Wiggins, Kerri L., Yanek, Lisa R., Yang, Ivana V., Young, Kendra A., Young, Kristin L., Zhang, Yingze, Liu, Dajiang J., Keller, Matthew C., Vrieze, Scott

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Inherited Causes of Clonal Haematopoiesis in 97,691 Whole Genomes von Bick, Alexander, Weinstock, Joshua S, Nandakumar, Satish K, Fulco, Charles P, Zekavat, Seyedeh M, Szeto, Mindy D, Liao, Xiaotian, Leventhal, Matthew J, Nasser, Joseph, Chang, Kyle, Laurie, Cecelia, Burugula, Bala Bharathi, Gibson, Christopher J, Lin, Amy, Taub, Margaret A, Aguet, Francois, Mitchell, Braxton D, Barnes, Kathleen C, Moscati, Arden, Fornage, Myriam, Redline, Susan, Silverman, Edwin, Weiss, Scott, Palmer, Nicholette D, Kardia, Sharon L. R, He, Jiang, Kaplan, Robert C, Smith, Nicholas L, Arnett, Donna K, Correa, Adolfo, Guo, Xiuqing, Konkle, Barbara A, Custer, Brian, Peralta, Juan M, Meyers, Deborah A, McGarvey, Stephen T, Chen, Ida Yii-Der, Shoemaker, M. Benjamin, Wang, Fei Fei, Wong, Quenna, Daya, Michelle, Kenny, Eimear E, Launer, Lenore J, Cade, Brian, Bis, Joshua C, Cho, Michael, Cupples, L. Adrienne, Mak, Angel C. Y, Becker, Lewis C, Smith, Jennifer A, Heckbert, Susan R, Yang, Ivana V, Heit, John A, Lubitz, Steven, Johnsen, Jill M, Wenzel, Sally E, Weeks, Daniel E, Rao, Dabeeru C, Darbar, Dawood, Buth, Erin J, Rafaels, Nicholas, Loos, Ruth J. F, Hou, Lifang, Lee, Jiwon, Kachroo, Priyadarshini, Freedman, Barry I, Floyd, James S, Whitsel, Eric A, Ellinor, Patrick, Irvin, Marguerite R, Fingerlin, Tasha E, Raffield, Laura M, Armasu, Sebastian M, Wheeler, Marsha M, Sabino, Ester C, Blangero, John, Williams, L. Keoki, Levy, Bruce, Roden, Dan M, Manson, JoAnn, Mathias, Rasika A, Taylor, Kent D, Johnson, Andrew D, Auer, Paul L, Kooperberg, Charles, Laurie, Cathy C, Blackwell, Thomas W, Zhao, Hongyu, Lange, Ethan, Rotter, Jerome I, Wilson, James G, Scheet, Paul, Kitzman, Jacob O, Lander, Eric, Engreitz, Jesse, Ebert, Benjamin, Reiner, Alexander P, Abecasis, Gonçalo, Kathiresan, Sekar, Natarajan, Pradeep

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Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma von Hecker, Julian, Cho, Michael H., Virkud, Yamini V., Burchard, Esteban G., Celedón, Juan C., Gui, Hongsheng, Soto-Quiros, Manuel E., Acosta-Pérez, Edna, Lange, Christoph, Weiss, Scott T., Abecasis, Goncalo, Alonso, Alvaro, Arking, Dan, Aslibekyan, Stella, Bielak, Larry, Borecki, Ingrid, Brody, Jennifer, Burchard, Esteban, Cardwell, Jonathan, Casaburi, Richard, Chaffin, Mark, Chasman, Daniel, Cupples, L. Adrienne, Curran, Joanne, Davis, Colleen, DeMeo, Dawn, Dutcher, Susan, Eaton, Charles, Emery, Leslie, Farnam, Leanna, Flickinger, Matthew, Franceschini, Nora, Fu, Mao, Fullerton, Stephanie M., Fulton, Lucinda, Gao, Yan, Germer, Soren, Guan, Yue, Harris, Daniel, Heavner, Ben, Heckbert, Susan, Hixson, James, Hong, Elliott, Hoth, Karin, Huston, Haley, Jackson, Rebecca, Jaquish, Cashell, Johnsen, Jill, Jones, Kimberly, Kaufman, Laura, Kelly, Shannon, Kinney, Greg, Krauter, Stephanie, Lange, Ethan, Lange, Leslie, LeFaive, Jonathon, Levy, Dan, Manson, JoAnn, McGarvey, Stephen, Mei, Hao, Mychaleckyj, Josyf C., Nickerson, Deborah, Parker, Margaret, Parsa, Afshin, Peralta, Juan Manuel, Perry, James, Post, Wendy, Rao, D.C., Reiner, Alex, Roselli, Carolina, Rotter, Jerome, Salimi, Shabnam, Salzberg, Steven, Sandow, Kevin, Scheller, Christopher, Schwander, Karen, Seidman, Christine, Seidman, Jonathan, Sheu, Wayne Hui-Heng, Smith, Nicholas, Sotoodehnia, Nona, Stilp, Adrienne, Sung, Yun Ju, Sylvia, Jody, Szpiro, Adam, Tang, Hua, Taub, Margaret, Taylor, Kent, Tinker, Lesley, Vrieze, Scott, Wallace, Robert, Wan, Emily, Wang, Fei Fei, Watson, Karol, Xu, Huichun, Yanek, Lisa, Zhao, Wei, Zheng, Xiuwen, Zody, Michael, Zoellner, Sebastian

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Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries von Zekavat, Seyedeh M., Ruotsalainen, Sanni, Handsaker, Robert E., Alver, Maris, Bloom, Jonathan, Poterba, Timothy, Seed, Cotton, Ernst, Jason, Chaffin, Mark, Engreitz, Jesse, Peloso, Gina M., Manichaikul, Ani, Yang, Chaojie, Ryan, Kathleen A., Fu, Mao, Johnson, W. Craig, Tsai, Michael, Budoff, Matthew, Vasan, Ramachandran S., Cupples, L. Adrienne, Rotter, Jerome I., Rich, Stephen S., Post, Wendy, Mitchell, Braxton D., Correa, Adolfo, Metspalu, Andres, Wilson, James G., Salomaa, Veikko, Kellis, Manolis, Daly, Mark J., Neale, Benjamin M., McCarroll, Steven, Surakka, Ida, Esko, Tonu, Ganna, Andrea, Ripatti, Samuli, Kathiresan, Sekar, Natarajan, Pradeep

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