Including Vulnerable Populations in the Assessment of Data From Vulnerable Populations von Jackson, Latifa, Kuhlman, Caitlin, Jackson, Fatimah, Fox, P Keolu

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Functional EPAS1 / HIF2A missense variant is associated with hematocrit in Andean highlanders von Lawrence, Elijah S, Gu, Wanjun, Bohlender, Ryan J, Anza-Ramirez, Cecilia, Cole, Amy M, Yu, James J, Hu, Hao, Heinrich, Erica C, O'Brien, Katie A, Vasquez, Carlos A, Cowan, Quinn T, Bruck, Patrick T, Mercader, Kysha, Alotaibi, Mona, Long, Tao, Hall, James E, Moya, Esteban A, Bauk, Marco A, Reeves, Jennifer J, Kong, Mitchell C, Salem, Rany M, Vizcardo-Galindo, Gustavo, Macarlupu, Jose-Luis, Figueroa-Mujíca, Rómulo, Bermudez, Daniela, Corante, Noemi, Gaio, Eduardo, Fox, Keolu P, Salomaa, Veikko, Havulinna, Aki S, Murray, Andrew J, Malhotra, Atul, Powel, Frank L, Jain, Mohit, Komor, Alexis C, Cavalleri, Gianpiero L, Huff, Chad D, Villafuerte, Francisco C, Simonson, Tatum S

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ABO Genetic Variation in Neanderthals and Denisovans von Villanea, Fernando A, Huerta-Sanchez, Emilia, Fox, Keolu

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Rare loss of function variants in candidate genes and risk of colorectal cancer von Rosenthal, Elisabeth A., Shirts, Brian H., Amendola, Laura M., Horike-Pyne, Martha, Robertson, Peggy D., Hisama, Fuki M., Bennett, Robin L., Dorschner, Michael O., Nickerson, Deborah A., Stanaway, Ian B., Nassir, Rami, Vickers, Kathy T., Li, Christopher, Grady, William M., Peters, Ulrike, Jarvik, Gail P.

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Functional EPAS1/HIF2A missense variant is associated with hematocrit in Andean highlanders von Lawrence, Elijah S, Gu, Wanjun, Bohlender, Ryan J, Anza-Ramirez, Cecilia, Cole, Amy M, Yu, James J, Hu, Hao, Heinrich, Erica C, O'Brien, Katie A, Vasquez, Carlos A, Cowan, Quinn T, Bruck, Patrick T, Mercader, Kysha, Alotaibi, Mona, Long, Tao, Hall, James E, Moya, Esteban A, Bauk, Marco A, Reeves, Jennifer J, Kong, Mitchell C, Salem, Rany M, Vizcardo-Galindo, Gustavo, Macarlupu, Jose-Luis, Figueroa-Mujíca, Rómulo, Bermudez, Daniela, Corante, Noemi, Gaio, Eduardo, Fox, Keolu P, Salomaa, Veikko, Havulinna, Aki S, Murray, Andrew J, Malhotra, Atul, Powel, Frank L, Jain, Mohit, Komor, Alexis C, Cavalleri, Gianpiero L, Huff, Chad D, Villafuerte, Francisco C, Simonson, Tatum S

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Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project von Johnsen, Jill M., Auer, Paul L., Morrison, Alanna C., Jiao, Shuo, Wei, Peng, Haessler, Jeffrey, Fox, Keolu, McGee, Sean R., Smith, Joshua D., Carlson, Christopher S., Smith, Nicholas, Boerwinkle, Eric, Kooperberg, Charles, Nickerson, Deborah A., Rich, Stephen S., Green, David, Peters, Ulrike, Cushman, Mary, Reiner, Alex P.

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Imputation of Exome Sequence Variants into Population-Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project von AUER, Paul L, JOHNSEN, Jill M, RICH, Stephen S, O'DONNELL, Christopher J, JACKSON, Rebecca D, WALLACE, Robert B, ZHAO CHEN, GRAUBERT, Timothy A, WILSON, James G, HUA TANG, LETTRE, Guillaume, REINER, Alex P, JOHNSON, Andrew D, GANESH, Santhi K, YUN LI, LOGSDON, Benjamin A, LANGE, Leslie A, NALLS, Michael A, GUOSHENG ZHANG, FRANCESCHINI, Nora, FOX, Keolu, LANGE, Ethan M

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SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function von Li, Man, Li, Yong, Weeks, Olivia, Mijatovic, Vladan, Teumer, Alexander, Huffman, Jennifer E, Tromp, Gerard, Fuchsberger, Christian, Gorski, Mathias, Lyytikäinen, Leo-Pekka, Nutile, Teresa, Sedaghat, Sanaz, Sorice, Rossella, Tin, Adrienne, Yang, Qiong, Ahluwalia, Tarunveer S, Arking, Dan E, Bihlmeyer, Nathan A, Böger, Carsten A, Carroll, Robert J, Chasman, Daniel I, Cornelis, Marilyn C, Dehghan, Abbas, Faul, Jessica D, Feitosa, Mary F, Gambaro, Giovanni, Gasparini, Paolo, Giulianini, Franco, Heid, Iris, Huang, Jinyan, Imboden, Medea, Jackson, Anne U, Jeff, Janina, Jhun, Min A, Katz, Ronit, Kifley, Annette, Kilpeläinen, Tuomas O, Kumar, Ashish, Laakso, Markku, Li-Gao, Ruifang, Lohman, Kurt, Lu, Yingchang, Mägi, Reedik, Malerba, Giovanni, Mihailov, Evelin, Mohlke, Karen L, Mook-Kanamori, Dennis O, Robino, Antonietta, Ruderfer, Douglas, Salvi, Erika, Schick, Ursula M, Schulz, Christina-Alexandra, Smith, Albert V, Smith, Jennifer A, Traglia, Michela, Yerges-Armstrong, Laura M, Zhao, Wei, Goodarzi, Mark O, Kraja, Aldi T, Liu, Chunyu, Wessel, Jennifer, Boerwinkle, Eric, Borecki, Ingrid B, Bork-Jensen, Jette, Bottinger, Erwin P, Braga, Daniele, Brandslund, Ivan, Brody, Jennifer A, Campbell, Archie, Carey, David J, Christensen, Cramer, Coresh, Josef, Crook, Errol, Curhan, Gary C, Cusi, Daniele, de Boer, Ian H, de Vries, Aiko P J, Denny, Joshua C, Devuyst, Olivier, Dreisbach, Albert W, Endlich, Karlhans, Esko, Tõnu, Franco, Oscar H, Fulop, Tibor, Gerhard, Glenn S, Glümer, Charlotte, Gottesman, Omri, Grarup, Niels, Gudnason, Vilmundur, Hansen, Torben, Harris, Tamara B, Hayward, Caroline, Hocking, Lynne, Hofman, Albert, Hu, Frank B, Husemoen, Lise Lotte N, Jackson, Rebecca D, Jørgensen, Torben, Jørgensen, Marit E, Kähönen, Mika

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Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis von Polfus, Linda M., Khajuria, Rajiv K., Schick, Ursula M., Pankratz, Nathan, Pazoki, Raha, Brody, Jennifer A., Chen, Ming-Huei, Auer, Paul L., Floyd, James S., Huang, Jie, Lange, Leslie, van Rooij, Frank J.A., Gibbs, Richard A., Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Walter, Klaudia, Chen, Lu, Yanek, Lisa, Becker, Lewis C., Peloso, Gina M., Wakabayashi, Aoi, Kals, Mart, Metspalu, Andres, Esko, Tõnu, Fox, Keolu, Wallace, Robert, Franceschini, Nora, Matijevic, Nena, Rice, Kenneth M., Bartz, Traci M., Lyytikäinen, Leo-Pekka, Kähönen, Mika, Lehtimäki, Terho, Raitakari, Olli T., Li-Gao, Ruifang, Mook-Kanamori, Dennis O., Lettre, Guillaume, van Duijn, Cornelia M., Franco, Oscar H., Rich, Stephen S., Rivadeneira, Fernando, Hofman, Albert, Uitterlinden, André G., Wilson, James G., Psaty, Bruce M., Soranzo, Nicole, Dehghan, Abbas, Boerwinkle, Eric, Zhang, Xiaoling, Johnson, Andrew D., O’Donnell, Christopher J., Johnsen, Jill M., Reiner, Alexander P., Ganesh, Santhi K., Sankaran, Vijay G.

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Analysis of exome sequencing data sets reveals structural variation in the coding region of ABO in individuals of African ancestry von Fox, Keolu, Johnsen, Jill M., Coe, Bradley P., Frazar, Chris D., Reiner, Alexander P., Eichler, Evan E., Nickerson, Deborah A.

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Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis von Polfus, Linda M., Khajuria, Rajiv K., Schick, Ursula M., Pankratz, Nathan, Pazoki, Raha, Brody, Jennifer A., Chen, Ming-Huei, Auer, Paul L., Floyd, James S., Huang, Jie, Lange, Leslie, van Rooij, Frank J.A., Gibbs, Richard A., Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Walter, Klaudia, Chen, Lu, Yanek, Lisa, Becker, Lewis C., Peloso, Gina M., Wakabayashi, Aoi, Kals, Mart, Metspalu, Andres, Esko, Tõnu, Fox, Keolu, Wallace, Robert, Franceschini, Nora, Matijevic, Nena, Rice, Kenneth M., Bartz, Traci M., Lyytikäinen, Leo-Pekka, Kähönen, Mika, Lehtimäki, Terho, Raitakari, Olli T., Li-Gao, Ruifang, Mook-Kanamori, Dennis O., Lettre, Guillaume, van Duijn, Cornelia M., Franco, Oscar H., Rich, Stephen S., Rivadeneira, Fernando, Hofman, Albert, Uitterlinden, André G., Wilson, James G., Psaty, Bruce M., Soranzo, Nicole, Dehghan, Abbas, Boerwinkle, Eric, Zhang, Xiaoling, Johnson, Andrew D., O’Donnell, Christopher J., Johnsen, Jill M., Reiner, Alexander P., Ganesh, Santhi K., Sankaran, Vijay G.

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