Lucas's Theorem and Some Related Results for Extended Pascal Triangles von Bollinger, Richard C., Burchard, Charles L.

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Lucas's Theorem and Some Related Results for Extended Pascal Triangles von Bollinger, Richard C., Burchard, Charles L.

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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program von Taliun, Daniel, Kessler, Michael D., Carlson, Jedidiah, Taliun, Sarah A. Gagliano, Kang, Hyun Min, Pitsillides, Achilleas N., Emde, Anne-Katrin, Clarke, Wayne E., Shetty, Amol C., Wong, Quenna, Bobo, Dean M., Aguet, François, Albert, Christine, Aslibekyan, Stella, Barnard, John, Barr, R. Graham, Barwick, Lucas, Becker, Lewis C., Bielak, Lawrence F., Blangero, John, Bowden, Donald W., Burchard, Esteban G., Chalazan, Brandon, Chasman, Daniel I., Chen, Yii-Der Ida, Choi, Seung Hoan, Chung, Mina K., Curran, Joanne E., Daya, Michelle, Ellinor, Patrick T., Fatkin, Diane, Fingerlin, Tasha, Forer, Lukas, Franceschini, Nora, Germer, Soren, Gladwin, Mark T., Hall, Michael E., He, Jiang, Johnsen, Jill M., Johnson, Andrew D., Kardia, Sharon L. R., Klemmer, Robert, Kooperberg, Charles, Köttgen, Anna, Lange, Leslie A., Lin, Xihong, Lin, Keng-Han, Liu, Chunyu, Loos, Ruth J. F., Gerszten, Robert, Lunetta, Kathryn L., Mak, Angel C. Y., Manichaikul, Ani, Manning, Alisa K., Mathias, Rasika A., McManus, David D., McGarvey, Stephen T., Meigs, James B., Minear, Mollie A., Mitchell, Braxton D., Mohanty, Sanghamitra, Montasser, May E., Montgomery, Courtney, Morrison, Alanna C., Murabito, Joanne M., Natale, Andrea, Nelson, Sarah C., Palmer, Nicholette D., Pankratz, Nathan, Peyser, Patricia A., Post, Wendy S., Psaty, Bruce M., Rao, D. C., Reiner, Alexander P., Roden, Dan, Rotter, Jerome I., Schoenherr, Sebastian, Seo, Jeong-Sun, Sheu, Wayne H., Smith, Nicholas L., Smith, Jennifer A., Stilp, Adrienne M., Telen, Marilyn, Thornton, Timothy A., Tracy, Russell P., Van Den Berg, David J., Vasan, Ramachandran S., Vrieze, Scott, Weng, Lu-Chen, Zhao, Xutong, Boerwinkle, Eric, Gibbs, Richard, Rich, Stephen S., Silverman, Edwin K., Qasba, Pankaj, Gan, Weiniu, Zöllner, Sebastian, Wilson, James G., Laurie, Cathy C., Jaquish, Cashell E.

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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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Novel Susceptibility Variants at 10p12.31-12.2 for Childhood Acute Lymphoblastic Leukemia in Ethnically Diverse Populations von HENG XU, WENJIAN YANG, HUNTSMAN, Scott, TORGERSON, Dara G, DEAN, Michael, WINICK, Naomi J, MARTIN, Paul L, CAMITTA, Bruce M, BOWMAN, W. Paul, WILLMAN, Cheryl L, CARROLL, William L, MULLIGHAN, Charles G, PEREZ-ANDREU, Virginia, BHOJWANI, Deepa, HUNGER, Stephen P, PUI, Ching-Hon, EVANS, William E, RELLING, Mary V, LOH, Mignon L, YANG, Jun J, DEVIDAS, Meenakshi, YIPING FAN, CHENG CHENG, DEQING PEI, SCHEET, Paul, BURCHARD, Esteban González, ENG, Celeste

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Novel susceptibility variants at the ERG locus for childhood acute lymphoblastic leukemia in Hispanics von Qian, Maoxiang, Xu, Heng, Perez-Andreu, Virginia, Roberts, Kathryn G., Zhang, Hui, Yang, Wenjian, Zhang, Shouyue, Zhao, Xujie, Smith, Colton, Devidas, Meenakshi, Gastier-Foster, Julie M., Raetz, Elizabeth, Larsen, Eric, Burchard, Esteban G., Winick, Naomi, Bowman, W. Paul, Martin, Paul L., Borowitz, Michael, Wood, Brent, Antillon-Klussmann, Federico, Pui, Ching-Hon, Mullighan, Charles G., Evans, William E., Hunger, Stephen P., Relling, Mary V., Loh, Mignon L., Yang, Jun J.

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A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adults von Perez-Andreu, Virginia, Roberts, Kathryn G., Xu, Heng, Smith, Colton, Zhang, Hui, Yang, Wenjian, Harvey, Richard C., Payne-Turner, Debbie, Devidas, Meenakshi, Cheng, I-Ming, Carroll, William L., Heerema, Nyla A., Carroll, Andrew J., Raetz, Elizabeth A., Gastier-Foster, Julie M., Marcucci, Guido, Bloomfield, Clara D., Mrózek, Krzysztof, Kohlschmidt, Jessica, Stock, Wendy, Kornblau, Steven M., Konopleva, Marina, Paietta, Elisabeth, Rowe, Jacob M., Luger, Selina M., Tallman, Martin S., Dean, Michael, Burchard, Esteban G., Torgerson, Dara G., Yue, Feng, Wang, Yanli, Pui, Ching-Hon, Jeha, Sima, Relling, Mary V., Evans, William E., Gerhard, Daniela S., Loh, Mignon L., Willman, Cheryl L., Hunger, Stephen P., Mullighan, Charles G., Yang, Jun J.

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Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse von Perez-Andreu, Virginia, Roberts, Kathryn G, Harvey, Richard C, Yang, Wenjian, Cheng, Cheng, Pei, Deqing, Xu, Heng, Gastier-Foster, Julie, E, Shuyu, Lim, Joshua Yew-Suang, Chen, I-Ming, Fan, Yiping, Devidas, Meenakshi, Borowitz, Michael J, Smith, Colton, Neale, Geoffrey, Burchard, Esteban G, Torgerson, Dara G, Klussmann, Federico Antillon, Villagran, Cesar Rolando Najera, Winick, Naomi J, Camitta, Bruce M, Raetz, Elizabeth, Wood, Brent, Yue, Feng, Carroll, William L, Larsen, Eric, Bowman, W Paul, Loh, Mignon L, Dean, Michael, Bhojwani, Deepa, Pui, Ching-Hon, Evans, William E, Relling, Mary V, Hunger, Stephen P, Willman, Cheryl L, Mullighan, Charles G, Yang, Jun J

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Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes von Keener, Rebecca, Chhetri, Surya B., Connelly, Carla J., Taub, Margaret A., Conomos, Matthew P., Weinstock, Joshua, Ni, Bohan, Strober, Benjamin, Aslibekyan, Stella, Auer, Paul L., Barwick, Lucas, Becker, Lewis C., Blangero, John, Bleecker, Eugene R., Brody, Jennifer A., Cade, Brian E., Celedon, Juan C., Chang, Yi-Cheng, Cupples, L. Adrienne, Custer, Brian, Freedman, Barry I., Gladwin, Mark T., Heckbert, Susan R., Hou, Lifang, Irvin, Marguerite R., Isasi, Carmen R., Johnsen, Jill M., Kenny, Eimear E., Kooperberg, Charles, Minster, Ryan L., Naseri, Take, Viali, Satupa’itea, Nekhai, Sergei, Pankratz, Nathan, Peyser, Patricia A., Taylor, Kent D., Telen, Marilyn J., Wu, Baojun, Yanek, Lisa R., Yang, Ivana V., Albert, Christine, Arnett, Donna K., Ashley-Koch, Allison E., Barnes, Kathleen C., Bis, Joshua C., Blackwell, Thomas W., Boerwinkle, Eric, Burchard, Esteban G., Carson, April P., Chen, Zhanghua, Chen, Yii-Der Ida, Darbar, Dawood, de Andrade, Mariza, Ellinor, Patrick T., Fornage, Myriam, Gelb, Bruce D., Gilliland, Frank D., He, Jiang, Islam, Talat, Kaab, Stefan, Kardia, Sharon L. R., Kelly, Shannon, Konkle, Barbara A., Kumar, Rajesh, Loos, Ruth J. F., Martinez, Fernando D., McGarvey, Stephen T., Meyers, Deborah A., Mitchell, Braxton D., Montgomery, Courtney G., North, Kari E., Palmer, Nicholette D., Peralta, Juan M., Raby, Benjamin A., Redline, Susan, Rich, Stephen S., Roden, Dan, Rotter, Jerome I., Ruczinski, Ingo, Schwartz, David, Sciurba, Frank, Shoemaker, M. Benjamin, Silverman, Edwin K., Sinner, Moritz F., Smith, Nicholas L., Smith, Albert V., Tiwari, Hemant K., Vasan, Ramachandran S., Weiss, Scott T., Williams, L. Keoki, Zhang, Yingze, Ziv, Elad, Raffield, Laura M., Reiner, Alexander P., Arvanitis, Marios, Greider, Carol W., Mathias, Rasika A., Battle, Alexis

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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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Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25 von Fejerman, Laura, Ahmadiyeh, Nasim, Hu, Donglei, Huntsman, Scott, Beckman, Kenneth B., Caswell, Jennifer L., Tsung, Karen, John, Esther M., Torres-Mejia, Gabriela, Carvajal-Carmona, Luis, Echeverry, María Magdalena, Tuazon, Anna Marie D., Ramirez, Carolina, Gignoux, Christopher R., Eng, Celeste, Gonzalez-Burchard, Esteban, Henderson, Brian, Marchand, Loic Le, Kooperberg, Charles, Hou, Lifang, Agalliu, Ilir, Kraft, Peter, Lindström, Sara, Perez-Stable, Eliseo J., Haiman, Christopher A., Ziv, Elad

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A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth von Rappoport, Nadav, Toung, Jonathan, Hadley, Dexter, Wong, Ronald J., Fujioka, Kazumichi, Reuter, Jason, Abbott, Charles W., Oh, Sam, Hu, Donglei, Eng, Celeste, Huntsman, Scott, Bodian, Dale L., Niederhuber, John E., Hong, Xiumei, Zhang, Ge, Sikora-Wohfeld, Weronika, Gignoux, Christopher R., Wang, Hui, Oehlert, John, Jelliffe-Pawlowski, Laura L., Gould, Jeffrey B., Darmstadt, Gary L., Wang, Xiaobin, Bustamante, Carlos D., Snyder, Michael P., Ziv, Elad, Patsopoulos, Nikolaos A., Muglia, Louis J., Burchard, Esteban, Shaw, Gary M., O’Brodovich, Hugh M., Stevenson, David K., Butte, Atul J., Sirota, Marina

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Genome sequencing unveils a regulatory landscape of platelet reactivity von Keramati, Ali R., Chen, Ming-Huei, Rodriguez, Benjamin A. T., Yanek, Lisa R., Bhan, Arunoday, Gaynor, Brady J., Ryan, Kathleen, Brody, Jennifer A., Zhong, Xue, Wei, Qiang, Kammers, Kai, Kanchan, Kanika, Iyer, Kruthika, Kowalski, Madeline H., Pitsillides, Achilleas N., Cupples, L. Adrienne, Li, Bingshan, Schlaeger, Thorsten M., Shuldiner, Alan R., O’Connell, Jeffrey R., Ruczinski, Ingo, Mitchell, Braxton D., Faraday, Nauder, Taub, Margaret A., Becker, Lewis C., Lewis, Joshua P., Mathias, Rasika A., Johnson, Andrew D.

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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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Common Variants in Interleukin-1-Beta Gene Are Associated with Intracranial Hemorrhage and Susceptibility to Brain Arteriovenous Malformation von Kim, Helen, Hysi, Pirro G., Pawlikowska, Ludmila, Poon, Annie, Burchard, Esteban González, Zaroff, Jonathan G., Sidney, Stephen, Ko, Nerissa U., Achrol, Achal S., Lawton, Michael T., McCulloch, Charles E., Kwok, Pui-Yan, Young, William L.

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Whole genome sequence analyses of brain imaging measures in the Framingham Study von Sarnowski, Chloé, Satizabal, Claudia L, DeCarli, Charles, Pitsillides, Achilleas N, Cupples, L Adrienne, Vasan, Ramachandran S, Wilson, James G, Bis, Joshua C, Fornage, Myriam, Beiser, Alexa S, DeStefano, Anita L, Dupuis, Josée, Seshadri, Sudha

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Variant-specific inflation factors for assessing population stratification at the phenotypic variance level von Sofer, Tamar, Zheng, Xiuwen, Laurie, Cecelia A., Gogarten, Stephanie M., Brody, Jennifer A., Conomos, Matthew P., Bis, Joshua C., Thornton, Timothy A., Szpiro, Adam, O’Connell, Jeffrey R., Lange, Ethan M., Gao, Yan, Cupples, L. Adrienne, Psaty, Bruce M., Rice, Kenneth M.

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Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations von Daya, Michelle, Rafaels, Nicholas M., Brunetti, Tonya M., Chavan, Sameer, Levin, Albert M., Shetty, Aniket, Gignoux, Cristopher R., Boorgula, Meher Preethi, Wojcik, Genevieve, Campbell, Monica, Vergara, Candelaria I., Torgerson, Dara G., Ortega, Victor E., Doumatey, Ayo, Johnston, Henry R., Acevedo, Nathalie, Araujo, Maria A., Avila, Pedro C., Belbin, Gillian, Bleecker, Eugene R., Bustamante, Carlos, Caraballo, Luis, Cruz, Alvaro A., Dunston, Georgia M., Eng, Celeste, Faruque, Mezbah U., Ferguson, Trevor S., Figueiredo, Camila, Ford, Jean G., Gan, Weiniu, Gourraud, Pierre-Antoine, Hansel, Nadia, Hernandez, Ryan D., Herrera-Paz, Edwin P., Jimenez, Silvia, Kenny, Eimear E., Knight-Madden, Jennifer, Kumar, Rajesh, Lange, Leslie E., Lange, Ethan M., Lizee, Antoine, Maul, Pissamai, Maul, Trevor, Mayorga Sirera, Alvaro J., Meyers, Deborah A., Nicolae, Dan L., D O'Connor, Timothy, Oliveira, Ricardo R., Olopade, Christopher O., Olopade, Olufunmilayo, Qin, Zhaohui S., Rotimi, Charles, Vince, Nicolas, Watson, Harold, Wilks, Rainford J., Wilson, James G., Salzberg, Steven, Ober, Carole, Burchard, Esteban G., Williams, L. Keoki, Beaty, Terri H., Taub, Margaret A., Ruczinski, Ingo, Mathias, Rasika A., Barnes, Kathleen C.

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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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Polymorphisms in transforming growth factor-β-related genes ALK1 and ENG are associated with sporadic brain arteriovenous malformations von PAWLIKOWSKA, Ludmila, TRAN, Mary N, MARCHUK, Douglas, KWOK, Pui-Yan, YOUNG, William L, ACHROL, Achal S, HA, Connie, BURCHARD, Esteban, CHOUDHRY, Shweta, ZAROFF, Jonathan, LAWTON, Michael T, CASTRO, Richard, MCCULLOCH, Charles E

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