Electro‐kinetically driven route for highly sensitive blood pathology on a paper‐based device von Mani, Naresh Kumar, Das, Sankha Shuvra, Dawn, Sayantan, Chakraborty, Suman

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Control of Mass Flow-Rate of Viscoelastic Fluids Through Time-Periodic Electro-Osmotic Flows in a Microchannel von Dawn, Sayantan, Sarkar, Sandip

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A stable loosely coupled Fluid Structure Interaction scheme using sharp interface immersed boundary method for low to moderate mass ratios von Sarkar, Nandan, Dawn, Sayantan, Raj, Apurva, Khan, Piru Mohan, Roy, Somnath

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Electrokinetic Trapping of Microparticles Using Paper-and-Pencil Microfluidics von Das, Sankha Shuvra, Kar, Shantimoy, Dawn, Sayantan, Saha, Partha, Chakraborty, Suman

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Controlled Electrokinetic Particle Manipulation using Paper-and-Pencil Microfluidics von Das, Sankha Shuvra, Kar, Shantimoy, Sayantan Dawn, Saha, Partha, Chakraborty, Suman

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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., Burchard, Esteban G., 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., 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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Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale von Li, Xihao, Li, Zilin, Zhou, Hufeng, Gaynor, Sheila M., Liu, Yaowu, Chen, Han, Sun, Ryan, Dey, Rounak, Arnett, Donna K., Aslibekyan, Stella, Ballantyne, Christie M., Bielak, Lawrence F., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Broome, Jai G., Conomos, Matthew P., Correa, Adolfo, Cupples, L. Adrienne, Curran, Joanne E., Freedman, Barry I., Guo, Xiuqing, Hindy, George, Irvin, Marguerite R., Kardia, Sharon L. R., Kathiresan, Sekar, Khan, Alyna T., Kooperberg, Charles L., Laurie, Cathy C., Liu, X. Shirley, Mahaney, Michael C., Manichaikul, Ani W., Martin, Lisa W., Mathias, Rasika A., McGarvey, Stephen T., Mitchell, Braxton D., Montasser, May E., Moore, Jill E., Morrison, Alanna C., O’Connell, Jeffrey R., Palmer, Nicholette D., Pampana, Akhil, Peralta, Juan M., Peyser, Patricia A., Psaty, Bruce M., Redline, Susan, Rice, Kenneth M., Rich, Stephen S., Smith, Jennifer A., Tiwari, Hemant K., Tsai, Michael Y., Vasan, Ramachandran S., Wang, Fei Fei, Weeks, Daniel E., Weng, Zhiping, Wilson, James G., Yanek, Lisa R., Neale, Benjamin M., Sunyaev, Shamil R., Abecasis, Gonçalo R., Rotter, Jerome I., Willer, Cristen J., Peloso, Gina M., Natarajan, Pradeep, Lin, Xihong

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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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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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Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices von Natarajan, Pradeep, Pampana, Akhil, Graham, Sarah E., Ruotsalainen, Sanni E., Perry, James A., de Vries, Paul S., Broome, Jai G., Pirruccello, James P., Honigberg, Michael C., Aragam, Krishna, Wolford, Brooke, Brody, Jennifer A., Antonacci-Fulton, Lucinda, Arden, Moscati, Aslibekyan, Stella, Ballantyne, Christie M., Bielak, Lawrence F., Bis, Joshua C., Cade, Brian E., Do, Ron, Doddapaneni, Harsha, Emery, Leslie S., Hung, Yi-Jen, Irvin, Marguerite R., Khan, Alyna T., Lange, Leslie, Lee, Jiwon, Lemaitre, Rozenn N., Martin, Lisa W., Metcalf, Ginger, Montasser, May E., Moon, Jee-Young, Muzny, Donna, O’Connell, Jeffrey R., Palmer, Nicholette D., Peralta, Juan M., Peyser, Patricia A., Stilp, Adrienne M., Tsai, Michael, Wang, Fei Fei, Weeks, Daniel E., Yanek, Lisa R., Wilson, James G., Abecasis, Goncalo, Arnett, Donna K., Becker, Lewis C., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Chang, Yi-Cheng, Chen, Yii-Der I., Choi, Won Jung, Correa, Adolfo, Curran, Joanne E., Daly, Mark J., Dutcher, Susan K., Ellinor, Patrick T., Fornage, Myriam, Freedman, Barry I., Gabriel, Stacey, Germer, Soren, Gibbs, Richard A., He, Jiang, Hveem, Kristian, Jarvik, Gail P., Kaplan, Robert C., Kardia, Sharon L. R., Kenny, Eimear, Kim, Ryan W., Kooperberg, Charles, Laurie, Cathy C., Lee, Seonwook, Lloyd-Jones, Don M., Loos, Ruth J. F., Lubitz, Steven A., Mathias, Rasika A., Martinez, Karine A. Viaud, McGarvey, Stephen T., Mitchell, Braxton D., Nickerson, Deborah A., North, Kari E., Palotie, Aarno, Park, Cheol Joo, Psaty, Bruce M., Rao, D. C., Redline, Susan, Reiner, Alexander P., Seo, Daekwan, Seo, Jeong-Sun, Smith, Albert V., Tracy, Russell P., Vasan, Ramachandran S., Kathiresan, Sekar, Cupples, L. Adrienne, Rotter, Jerome I., Morrison, Alanna C., Rich, Stephen S., Ripatti, Samuli, Willer, Cristen, Peloso, Gina 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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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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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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Effect of Sickle Cell Trait and APOL1 Genotype on the Association of Soluble uPAR with Kidney Function Measures in Black Americans von Reiner, Alexander P, Raffield, Laura M, Franceschini, Nora, Auer, Paul L, Lange, Ethan M, Nickerson, Deborah A, Zakai, Neil A, Correa, Adolfo, Olson, Nels

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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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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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