Search Results - Bick, Jennifer L.

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    High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correla... by Rojnueangnit, Kitiwan, Xie, Jing, Gomes, Alicia, Sharp, Angela, Callens, Tom, Chen, Yunjia, Liu, Ying, Cochran, Meagan, Abbott, Mary-Alice, Atkin, Joan, Babovic-Vuksanovic, Dusica, Barnett, Christopher P., Crenshaw, Melissa, Bartholomew, Dennis W., Basel, Lina, Bellus, Gary, Ben-Shachar, Shay, Bialer, Martin G., Bick, David, Blumberg, Bruce, Cortes, Fanny, David, Karen L., Destree, Anne, Duat-Rodriguez, Anna, Earl, Dawn, Escobar, Luis, Eswara, Marthanda, Ezquieta, Begona, Frayling, Ian M., Frydman, Moshe, Gardner, Kathy, Gripp, Karen W., Hernández-Chico, Concepcion, Heyrman, Kurt, Ibrahim, Jennifer, Janssens, Sandra, Keena, Beth A, Llano-Rivas, Isabel, Leppig, Kathy, McDonald, Marie, Misra, Vinod K., Mulbury, Jennifer, Narayanan, Vinodh, Orenstein, Naama, Galvin-Parton, Patricia, Pedro, Helio, Pivnick, Eniko K., Powell, Cynthia M., Randolph, Linda, Raskin, Salmo, Rosell, Jordi, Rubin, Karol, Seashore, Margretta, Schaaf, Christian P., Scheuerle, Angela, Schultz, Meredith, Schorry, Elizabeth, Schnur, Rhonda, Siqveland, Elizabeth, Tkachuk, Amanda, Tonsgard, James, Upadhyaya, Meena, Verma, Ishwar C., Wallace, Stephanie, Williams, Charles, Zackai, Elaine, Zonana, Jonathan, Lazaro, Conxi, Claes, Kathleen, Korf, Bruce, Martin, Yolanda, Legius, Eric, Messiaen, Ludwine

    Published in Human mutation
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    Multicenter evaluation of the clinical utility of laparoscopy-assisted ERCP in patients with Roux-en-Y gastric bypass by Abbas, Ali M., Strong, Andrew T., Diehl, David L., Brauer, Brian C., Lee, Iris H., Burbridge, Rebecca, Zivny, Jaroslav, Higa, Jennifer T., Falcão, Marcelo, El Hajj, Ihab I., Tarnasky, Paul, Enestvedt, Brintha K., Ende, Alexander R., Thaker, Adarsh M., Pawa, Rishi, Jamidar, Priya, Sampath, Kartik, de Moura, Eduardo Guimarães Hourneaux, Kwon, Richard S., Suarez, Alejandro L., Aburajab, Murad, Wang, Andrew Y., Shakhatreh, Mohammad H., Kaul, Vivek, Kang, Lorna, Kowalski, Thomas E., Pannala, Rahul, Tokar, Jeffrey, Aadam, A. Aziz, Tzimas, Demetrios, Wagh, Mihir S., Draganov, Peter V., Ponsky, Jeffrey, Greenwald, Bruce D., Uradomo, Lance T., McGhan, Alyson A., Hakimian, Shahrad, Ross, Andrew, Sherman, Stuart, Bick, Benjamin L., Forsmark, Christopher E., Yang, Dennis, Gupte, Anand, Chauhan, Shailendra, Hughes, Steven J., Saks, Karen, Bakis, Gennadiy, Templeton, Adam W., Saunders, Michael, Sedarat, Alireza, Evans, John A., Muniraj, Thiruvengadam, Gardner, Timothy B., Ramos, Almino C., Santo, Marco Aurelio, Nett, Andrew, Coté, Gregory A., Elmunzer, B. Joseph, Dua, Kulwinder S., Nosler, Michael J., Strand, Daniel S., Yeaton, Paul, Kothari, Shivangi, Ullah, Asad, Taunk, Pushpak, Brady, Patrick, Pinkas, Haim, Faulx, Ashley L., Shahid, Haroon, Holmes, Jordan, Pannu, Davinderbir, Komanduri, Srinadh, Bucobo, Juan Carlos, Dhaliwal, Harry, Rostom, Alaa, Acker, Brent W.

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    Inherited Causes of Clonal Hematopoiesis in 97,691 TOPMed Whole Genomes by 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.

    Published in Nature (London)
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    Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes by Bick, Alexander G, Weinstock, Joshua S, Nandakumar, Satish K, Fulco, Charles P, Zekavat, Seyedeh M, Szeto, Mindy D, Leventhal, Matthew J, Nasser, Joseph, Chang, Kyle, Laurie, Cecelia, Burugula, Bala Bharathi, Gibson, Christopher J, Niroula, Abhishek, Taub, Margaret A, Aguet, Francois, Ardlie, Kristin, Mitchell, Braxton D, Barnes, Kathleen C, Moscati, Arden, Psaty, Bruce M, 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, 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, Montasser, May E, Kenny, Eimear E, Cade, Brian E, Bis, Joshua C, Cho, Michael H, Lasky-Su, Jessica, Bowden, Donald W, Cupples, L Adrienne, Mak, Angel C Y, Becker, Lewis C, Smith, Jennifer A, Kelly, Tanika N, Aslibekyan, Stella, Yang, Ivana V, Heit, John A, Lubitz, Steven A, Curran, Joanne E, Wenzel, Sally E, Rao, Dabeeru C, Darbar, Dawood, Tracy, Russell P, Loos, Ruth J F, Durda, Peter, Liu, Yongmei, Hou, Lifang, Lee, Jiwon, Freedman, Barry I, Levy, Daniel, Bielak, Lawrence F, Hixson, James E, Floyd, James S, Ellinor, Patrick T, Irvin, Marguerite R, Fingerlin, Tasha E, Armasu, Sebastian M, Sabino, Ester C, Blangero, John, Williams, L Keoki, Levy, Bruce D, Sheu, Wayne Huey-Herng, Roden, Dan M, Manson, JoAnn E, Taylor, Kent D, Kooperberg, Charles, Laurie, Cathy C, Blackwell, Thomas W, Smith, Albert V, Zhao, Hongyu, Lange, Leslie, Rich, Stephen S, Wilson, James G, Scheet, Paul, Lander, Eric S, Engreitz, Jesse M, Ebert, Benjamin L, Reiner, Alexander P, Abecasis, Gonçalo, Kathiresan, Sekar, Natarajan, Pradeep

    Published in Nature (London)
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    The genetic determinants of recurrent somatic mutations in 43,693 blood genomes by Weinstock, Joshua S, Laurie, Cecelia A, Broome, Jai G, Taylor, Kent D, Guo, Xiuqing, Shuldiner, Alan R, O'Connell, Jeffrey R, Lewis, Joshua P, Boerwinkle, Eric, Barnes, Kathleen C, Chami, Nathalie, Kenny, Eimear E, Loos, Ruth J F, Fornage, Myriam, Redline, Susan, Cade, Brian E, Gilliland, Frank D, Chen, Zhanghua, Gauderman, W James, Kumar, Rajesh, Grammer, Leslie, Schleimer, Robert P, Psaty, Bruce M, Bis, Joshua C, Brody, Jennifer A, Silverman, Edwin K, Yun, Jeong H, Qiao, Dandi, Weiss, Scott T, Lasky-Su, Jessica, DeMeo, Dawn L, Palmer, Nicholette D, Freedman, Barry I, Bowden, Donald W, Cho, Michael H, Vasan, Ramachandran S, Johnson, Andrew D, Yanek, Lisa R, Becker, Lewis C, Kardia, Sharon, He, Jiang, Kaplan, Robert, Heckbert, Susan R, Smith, Nicholas L, Wiggins, Kerri L, Arnett, Donna K, Irvin, Marguerite R, Tiwari, Hemant, Correa, Adolfo, Raffield, Laura M, Gao, Yan, de Andrade, Mariza, Rotter, Jerome I, Rich, Stephen S, Manichaikul, Ani W, Konkle, Barbara A, Johnsen, Jill M, Wheeler, Marsha M, Custer, Brian S, Duggirala, Ravindranath, Curran, Joanne E, Blangero, John, Gui, Hongsheng, Xiao, Shujie, Williams, L Keoki, Meyers, Deborah A, Li, Xingnan, Ortega, Victor, McGarvey, Stephen, Gu, C Charles, Chen, Yii-Der Ida, Lee, Wen-Jane, Shoemaker, M Benjamin, Darbar, Dawood, Roden, Dan, Albert, Christine, Kooperberg, Charles, Desai, Pinkal, Blackwell, Thomas W, Abecasis, Goncalo R, Smith, Albert V, Kang, Hyun M, Mathias, Rasika, Natarajan, Pradeep, Jaiswal, Siddhartha, Reiner, Alexander P, Bick, Alexander G

    Published in Science advances
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