المؤلفون: Rael, Victoria E., Yano, Julian A., Huizar, John P., Slayden, Leianna C., Weiss, Madeleine A., Turcotte, Elizabeth A., Terry, Jacob M., Zuo, Wenqi, Thiffault, Isabelle, Pastinen, Tomi, Farrow, Emily G., Jenkins, Janda L., Becker, Mara L., Wong, Stephen C., Stevens, Anne M., Otten, Catherine, Allenspach, Eric J., Bonner, Devon E., Bernstein, Jonathan A., Wheeler, Matthew T., Saxton, Robert A., Acosta, Maria T., Adams, David R., Alvarez, Raquel L., Alvey, Justin, Allworth, Aimee, Andrews, Ashley, Ashley, Euan A., Afzali, Ben, Bacino, Carlos A., Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bale, Jim, Bamshad, Michael, Barbouth, Deborah, Bayrak-Toydemir, Pinar, Beck, Anita, Beggs, Alan H., Behrens, Edward, Bejerano, Gill, Bellen, Hugo J., Bennett, Jimmy, Berry, Gerard T., Bican, Anna, Bivona, Stephanie, Blue, Elizabeth, Bohnsack, John, Bonner, Devon

المساهمون: Lupus Research Institute, National Institutes of Health, Howard Hughes Medical Institute, National Science Foundation, Children’s Mercy Research Institute, Office of Strategic Coordination, Office of the NIH, Chan-Zuckerburg Biohub Physician Scientist Fellowship Program, Centers for Disease Control and Prevention

المصدر: Journal of Experimental Medicine ; volume 221, issue 8 ; ISSN 0022-1007 1540-9538

الاتاحة: http://dx.doi.org/10.1084/jem.20232005
https://rupress.org/jem/article-pdf/doi/10.1084/jem.20232005/1928690/jem_20232005.pdf

المؤلفون: Pucel, Jenna, Briere, Lauren C., Reuter, Chloe, Gochyyev, Perman, Acosta, Maria T., Adams, David R., Alvarez, Raquel L., Alvey, Justin, Allworth, Aimee, Andrews, Ashley, Ashley, Euan A., Bacino, Carlos A., Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bale, Jim, Bamshad, Michael, Barbouth, Deborah, Bayrak-Toydemir, Pinar, Beck, Anita, Beggs, Alan H., Behrens, Edward, Bejerano, Gill, Bellen, Hugo J., Bennett, Jimmy, Bernstein, Jonathan A., Berry, Gerard T., Bican, Anna, Bivona, Stephanie, Blue, Elizabeth, Bohnsack, John, Bonner, Devon, Botto, Lorenzo, Brown, Gabrielle, Burke, Elizabeth A., Burrage, Lindsay C., Butte, Manish J., Byers, Peter, Byrd, William E., Carey, John, Carrasquillo, Olveen, Cassini, Thomas, Peter Chang, Ta Chen, Chanprasert, Sirisak, Chao, Hsiao-Tuan, Chinn, Ivan, Clark, Gary D., Coakley, Terra R., Cobban, Laurel A.

المساهمون: National Institutes of Health

المصدر: Genetics in Medicine ; volume 26, issue 6, page 101115 ; ISSN 1098-3600

الاتاحة: http://dx.doi.org/10.1016/j.gim.2024.101115
https://api.elsevier.com/content/article/PII:S1098360024000480?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1098360024000480?httpAccept=text/plain

المؤلفون: Scala, Marcello, Tomati, Valeria, Ferla, Matteo, Lena, Mariateresa, Cohen, Julie S., Fatemi, Ali, Brokamp, Elly, Bican, Anna, Phillips, John A., Koziura, Mary E., Nicouleau, Michael, Rio, Marlene, Siquier, Karine, Boddaert, Nathalie, Musante, Ilaria, Tamburro, Serena, Baldassari, Simona, Iacomino, Michele, Scudieri, Paolo, Rosenfeld, Jill A., Bellus, Gary, Reed, Sara, Al Saif, Hind, Russo, Rossana Sanchez, Walsh, Matthew B., Cantagrel, Vincent, Crunk, Amy, Gustincich, Stefano, Ruggiero, Sarah M., Fitzgerald, Mark P., Helbig, Ingo, Striano, Pasquale, Severino, Mariasavina, Salpietro, Vincenzo, Pedemonte, Nicoletta, Zara, Federico, Acosta, Maria T., Adams, David R., Alvarez, Raquel L., Alvey, Justin, Allworth, Aimee, Andrews, Ashley, Ashley, Euan A., Afzali, Ben, Bacino, Carlos A., Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bale, Jim, Bamshad, Michael

المساهمون: Fondazione Compagnia di San Paolo, NIH Common Fund, Rosetrees Trust, Ministero della Salute

المصدر: The American Journal of Human Genetics ; volume 111, issue 3, page 529-543 ; ISSN 0002-9297

الاتاحة: http://dx.doi.org/10.1016/j.ajhg.2024.02.001
https://api.elsevier.com/content/article/PII:S0002929724000338?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0002929724000338?httpAccept=text/plain

المؤلفون: Lenahan, Arthur, Glass, Ian, Stergachis, Andrew, Paschal, Cate, Blue, Elizabeth, Allworth, Aimee, Cristian, Ingrid, Miller, Danny, Morrison, Jennifer

المصدر: Genetics in Medicine Open ; volume 2, page 101258 ; ISSN 2949-7744

الاتاحة: http://dx.doi.org/10.1016/j.gimo.2024.101258
https://api.elsevier.com/content/article/PII:S2949774424004047?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S2949774424004047?httpAccept=text/plain

المؤلفون: Borja, Nicholas A., Tinker, Rory J., Bivona, Stephanie A., Smith, Carson A., Locker, Theodore Krijnse, Fernandes, Samuela, Acosta, Maria T., Adams, David R., Afzali, Ben, Al‐Beshri, Ali, Allworth, Aimee, Alvarez, Raquel L., Alvey, Justin, Andrews, Ashley, Ashley, Euan A., Bacino, Carlos A., Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bale, Jim

المصدر: American Journal of Medical Genetics. Part A; Feb2025, Vol. 197 Issue 2, p1-7, 7p

المؤلفون: Fitzsimmons, Lane, Acosta, Maria T., Adams, David R., Afzali, Ben, Al-Beshri, Ali, Allenspach, Eric, Allworth, Aimee, Alvarez, Raquel L., Alvey, Justin, Andrews, Ashley, Ashley, Euan A., Bacino, Carlos A., Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Baldwin, Erin, Bale, Jim, Bamshad, Michael, Barbouth, Deborah, Bayrak-Toydemir, Pinar

المصدر: BioData Mining; 1/17/2025, Vol. 18 Issue 1, p1-16, 16p

مصطلحات موضوعية: PATIENTS' attitudes, RARE diseases, GENETIC variation, PHENOTYPES, SEIZURES (Medicine)

المؤلفون: Clayton, Ellen W., Linder, Jodell E., Allworth, Aimee, Bland, Sara T., others., 100

المصدر: Vanderbilt Law School Faculty Publications

مصطلحات موضوعية: Common variants, Family history, Genotyping, Monogenic risks, Polygenic risk scores, Computer Law, Health Law and Policy, Law

وصف الملف: application/pdf

Relation: https://scholarship.law.vanderbilt.edu/faculty-publications/1330; https://scholarship.law.vanderbilt.edu/context/faculty-publications/article/2353/viewcontent/Returning__integrated_genomic_risk_and_clinical_recommendations.pdf

الاتاحة: https://scholarship.law.vanderbilt.edu/faculty-publications/1330
https://scholarship.law.vanderbilt.edu/context/faculty-publications/article/2353/viewcontent/Returning__integrated_genomic_risk_and_clinical_recommendations.pdf

المؤلفون: Pujol-Giménez, Jonai, Mirzaa, Ghayda, Blue, Elizabeth E, Albano, Giuseppe, Miller, Danny E, Allworth, Aimee, Bennett, James T, Byers, Peter H, Chanprasert, Sirisak, Chen, Jingheng, Doherty, Daniel, Folta, Andrew B, Gillentine, Madelyn A, Glass, Ian, Hing, Anne, Horike-Pyne, Martha, Leppig, Kathleen A, Parhin, Azma, Ranchalis, Jane, Raskind, Wendy H, Rosenthal, Elisabeth A, Schwarze, Ulrike, Sheppeard, Sam, Strohbehn, Samuel, Sybert, Virginia P, Timms, Andrew, Wener, Mark, Bamshad, Michael J, Hisama, Fuki M, Jarvik, Gail P, Dipple, Katrina M, Hediger, Matthias A., Stergachis, Andrew B

المصدر: Pujol-Giménez, Jonai; Mirzaa, Ghayda; Blue, Elizabeth E; Albano, Giuseppe; Miller, Danny E; Allworth, Aimee; Bennett, James T; Byers, Peter H; Chanprasert, Sirisak; Chen, Jingheng; Doherty, Daniel; Folta, Andrew B; Gillentine, Madelyn A; Glass, Ian; Hing, Anne; Horike-Pyne, Martha; Leppig, Kathleen A; Parhin, Azma; Ranchalis, Jane; Raskind, Wendy H; . (2023). Dominant-negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome. Annals of Clinical and Translational Neurology, 10(6), pp. 1046-1053. Wiley 10.1002/acn3.51786

مصطلحات موضوعية: 610 Medicine & health

وصف الملف: application/pdf

Relation: https://boris.unibe.ch/182661/

الاتاحة: https://boris.unibe.ch/182661/1/Ann_Clin_Transl_Neurol_-_2023_-_Pujol_Gim_nez_-_Dominant_negative_variant_in_SLC1A4_causes_an_autosomal_dominant_epilepsy.pdf
https://boris.unibe.ch/182661/

المؤلفون: Pujol‐Giménez, Jonai, Mirzaa, Ghayda, Blue, Elizabeth E., Albano, Giuseppe, Miller, Danny E., Allworth, Aimee, Bennett, James T., Byers, Peter H., Chanprasert, Sirisak, Chen, Jingheng, Doherty, Daniel, Folta, Andrew B., Gillentine, Madelyn A., Glass, Ian, Hing, Anne, Horike‐Pyne, Martha, Leppig, Kathleen A., Parhin, Azma, Ranchalis, Jane, Raskind, Wendy H., Rosenthal, Elisabeth A., Schwarze, Ulrike, Sheppeard, Sam, Strohbehn, Samuel, Sybert, Virginia P., Timms, Andrew, Wener, Mark, Bamshad, Michael J., Hisama, Fuki M., Jarvik, Gail P., Dipple, Katrina M., Hediger, Matthias A., Stergachis, Andrew B.

المساهمون: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, National Institutes of Health, Burroughs Wellcome Fund, National Human Genome Research Institute

المصدر: Annals of Clinical and Translational Neurology ; volume 10, issue 6, page 1046-1053 ; ISSN 2328-9503 2328-9503

الاتاحة: http://dx.doi.org/10.1002/acn3.51786
https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.51786

المؤلفون: Linder, Jodell E., Allworth, Aimee, Bland, Harris T., Caraballo, Pedro J., Chisholm, Rex L., Clayton, Ellen Wright, Crosslin, David R., Dikilitas, Ozan, DiVietro, Alanna, Esplin, Edward D., Forman, Sophie, Freimuth, Robert R., Gordon, Adam S., Green, Richard, Harden, Maegan V., Holm, Ingrid A., Jarvik, Gail P., Karlson, Elizabeth W., Labrecque, Sofia, Lennon, Niall J., Limdi, Nita A., Mittendorf, Kathleen F., Murphy, Shawn N., Orlando, Lori, Prows, Cynthia A., Rasmussen, Luke V., Rasmussen-Torvik, Laura, Rowley, Robb, Sawicki, Konrad Teodor, Schmidlen, Tara, Terek, Shannon, Veenstra, David, Velez Edwards, Digna R., Absher, Devin, Abul-Husn, Noura S., Alsip, Jorge, Bangash, Hana, Beasley, Mark, Below, Jennifer E., Berner, Eta S., Booth, James, Chung, Wendy K., Cimino, James J., Connolly, John, Davis, Patrick, Devine, Beth, Fullerton, Stephanie M., Guiducci, Candace, Habrat, Melissa L., Hain, Heather

المساهمون: Cincinnati Children's Hospital Medical Center, National Human Genome Research Institute, Icahn School of Medicine at Mount Sinai, Mayo Clinic, University of Washington, Children's Hospital of Philadelphia, Vanderbilt University Medical Center, Columbia University, Northwestern University

المصدر: Genetics in Medicine ; volume 25, issue 4, page 100006 ; ISSN 1098-3600

الاتاحة: http://dx.doi.org/10.1016/j.gim.2023.100006
https://api.elsevier.com/content/article/PII:S1098360023000023?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1098360023000023?httpAccept=text/plain

المؤلفون: Connolly, John J., Berner, Eta S., Smith, Maureen, Levy, Samuel, Terek, Shannon, Harr, Margaret, Karavite, Dean, Suckiel, Sabrina, Holm, Ingrid A., Dufendach, Kevin, Nelson, Catrina, Khan, Atlas, Chisholm, Rex L., Allworth, Aimee, Wei, Wei-Qi, Bland, Harris T., Clayton, Ellen Wright, Soper, Emily R., Linder, Jodell E., Limdi, Nita A., Miller, Alexandra, Nigbur, Scott, Bangash, Hana, Hamed, Marwan, Sherafati, Alborz, Lewis, Anna C.F., Perez, Emma, Orlando, Lori A., Rakhra-Burris, Tejinder K., Al-Dulaimi, Mustafa, Cifric, Selma, Scherr, Courtney Lynam, Wynn, Julia, Hakonarson, Hakon, Sabatello, Maya

المساهمون: Northwestern University, National Human Genome Research Institute, Cincinnati Children's Hospital Medical Center, Mayo Clinic, Icahn School of Medicine at Mount Sinai, Children's Hospital of Philadelphia, University of Washington, Columbia University, Vanderbilt University Medical Center, Duke University

المصدر: Genetics in Medicine ; volume 25, issue 9, page 100906 ; ISSN 1098-3600

الاتاحة: http://dx.doi.org/10.1016/j.gim.2023.100906
https://api.elsevier.com/content/article/PII:S109836002300919X?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S109836002300919X?httpAccept=text/plain

المؤلفون: Allworth, Aimee, Glass, Ian, Hing, Anne, Blue, Elizabeth, Rosenthal, Elisabeth, Strohbehn, Sam, Jarvik, Gail, Dipple, Katrina, Stergachis, Andrew, Sybert, Virginia, Ranchalis, Jane, Horike-Pyne, Martha, Chanprasert, Sirisak, Hisama, Fuki, Bamshad, Michael, Bennett, James, Brandling-Bennett, Heather, Cabrera, Michelle, Wener, Mark

المصدر: Genetics in Medicine Open ; volume 1, issue 1, page 100128 ; ISSN 2949-7744

الاتاحة: http://dx.doi.org/10.1016/j.gimo.2023.100128
https://api.elsevier.com/content/article/PII:S2949774423001280?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S2949774423001280?httpAccept=text/plain

المؤلفون: McNamee, Lucy, Schoch, Kelly, Huang, Alden, Lee, Hane, Wang, Lee‐kai, Smith, Edward C., Lark, Robert K., Buckley, Anne F., Jobanputra, Vaidehi, Nelson, Stanley F., Shashi, Vandana, Acosta, Maria T., Adams, David R., Afzali, Ben, Al‐Beshri, Ali, Allenspach, Eric, Allworth, Aimee, Alvarez, Raquel L., Alvey, Justin, Andrews, Ashley

المصدر: American Journal of Medical Genetics. Part A; Nov2024, Vol. 194 Issue 11, p1-7, 7p

المؤلفون: Stellacci, Emilia, Carter, Jennefer N., Pannone, Luca, Stevenson, David, Moslehi, Dorsa, Venanzi, Serenella, Acosta, Maria T., Adams, David R., Afzali, Ben, Al‐Beshri, Ali, Allenspach, Eric, Allworth, Aimee, Alvarez, Raquel L., Alvey, Justin, Andrews, Ashley, Ashley, Euan A., Bacino, Carlos A., Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin

المصدر: American Journal of Medical Genetics. Part A; Aug2024, Vol. 194 Issue 8, p1-7, 7p

المؤلفون: Ezell, Kimberly M., Tinker, Rory J., Furuta, Yutaka, Gulsevin, Alican, Bastarache, Lisa, Hamid, Rizwan, Cogan, Joy D., Rives, Lynette, Neumann, Serena, Corner, Brian, Kozuria, Mary, Phillips, John A., Adams, David R., Afzali, Ben, Al‐Beshri, Ali, Allworth, Aimee, Alvarez, Raquel L., Alvey, Justin, Andrews, Ashley, Ashley, Euan A.

المصدر: American Journal of Medical Genetics. Part A; Jul2024, Vol. 194 Issue 7, p1-6, 6p

المؤلفون: Ma, Mengqi, Zheng, Yiming, Lu, Shenzhao, Pan, Xueyang, Worley, Kim C., Burrage, Lindsay C., Blieden, Lauren S., Allworth, Aimee, Chen, Wei-Liang, Merla, Giuseppe, Mandriani, Barbara, Rosenfeld, Jill A., Li-Kroeger, David, Dutta, Debdeep, Yamamoto, Shinya, Wangler, Michael F., Glass, Ian A., Strohbehn, Sam, Blue, Elizabeth, Prontera, Paolo, Lalani, Seema R., Bellen, Hugo J.

الاتاحة: http://dx.doi.org/10.7554/elife.95887.1
https://elifesciences.org/reviewed-preprints/95887v1/pdf

المؤلفون: Dohrn, Maike F., Bademci, Guney, Rebelo, Adriana P., Jeanne, Médéric, Borja, Nicholas A., Beijer, Danique, Danzi, Matt C., Bivona, Stephanie A., Gueguen, Paul, Zafeer, Mohammad F., Tekin, Mustafa, Züchner, Stephan, Acosta, Maria T., Adams, David R., Afzali, Ben, Allworth, Aimee, Alvarez, Raquel L., Alvey, Justin, Andrews, Ashley, Ashley, Euan A.

المصدر: Annals of Clinical & Translational Neurology; Apr2024, Vol. 11 Issue 4, p1075-1079, 5p

مصطلحات موضوعية: DEVELOPMENTAL delay, INTELLECTUAL disabilities, AUTISM, GENETIC variation, NEUROLOGICAL disorders, CHILDREN with developmental disabilities, CHILDREN with autism spectrum disorders

المؤلفون: Stergachis, Andrew B., Blue, Elizabeth E., Gillentine, Madelyn A., Wang, Lee-Kai, Schwarze, Ulrike, Cortés, Adriana Sedeño, Ranchalis, Jane, Allworth, Aimee, Bland, Austin E., Chanprasert, Sirisak, Chen, Jingheng, Doherty, Daniel, Folta, Andrew B., Glass, Ian, Horike-Pyne, Martha, Huang, Alden Y., Khan, Alyna T., Leppig, Kathleen A., Miller, Danny E., Mirzaa, Ghayda, Parhin, Azma, Raskind, Wendy H., Rosenthal, Elisabeth A., Sheppeard, Sam, Strohbehn, Samuel, Sybert, Virginia P., Tran, Thao T., Wener, Mark H., Byers, Peter H. H., Nelson, Stanley F., Bamshad, Michael J., Dipple, Katrina M., Jarvik, Gail P., Hoppins, Suzanne, Hisama, Fuki M.

المصدر: Neurology Genetics ; volume 9, issue 5 ; ISSN 2376-7839

الاتاحة: http://dx.doi.org/10.1212/nxg.0000000000200090
https://www.neurology.org/doi/pdfdirect/10.1212/NXG.0000000000200090

المؤلفون: Huang, Yue, Jay, Kristy L., Yen-Wen Huang, Alden, Wan, Jijun, Jangam, Sharayu V., Chorin, Odelia, Rothschild, Annick, Barel, Ortal, Mariani, Milena, Iascone, Maria, Xue, Han, Acosta, Maria T., Adams, David R., Raquel, Alvarez, L., Alvey, Justin, Allworth, Aimee, Andrews, Ashley, Ashley, Euan A., Bacino, Carlos A., Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bale, Jim, Bamshad, Michael, Barbouth, Deborah, Bayrak-Toydemir, Pinar, Beck, Anita, Beggs, Alan H., Behrens, Edward, Bejerano, Gill, Bellen, Hugo J., Bennett, Jimmy, Bernstein, Jonathan A., Berry, Gerard T., Bican, Anna, Bivona, Stephanie, Blue, Elizabeth, Bohnsack, John, Bonner, Devon, Botto, Lorenzo, Briere, Lauren C., Brown, Gabrielle, Burke, Elizabeth A., Burrage, Lindsay C., Butte, Manish J., Byers, Peter, Byrd, William E., Carey, John, Carrasquillo, Olveen, Carvhalo Neto, George D., Cassini, Thomas, Peter Chang, Ta Chen, Chanprasert, Sirisak, Chao, Hsiao-Tuan, Chinn, Ivan, Clark, Gary D., Coakley, Terra R., Cobban, Laurel A., Cogan, Joy D., Coggins, Matthew, Cole, F. Sessions, Colley, Heather A., Cope, Heidi, Corona, Rosario, Craigen, William J., Crouse, Andrew B., Cunningham, Michael, D’Souza, Precilla, Dai, Hongzheng, Dasari, Surendra, Davis, Joie, Dayal, Jyoti G., Dell'Angelica, Esteban C., Dipple, Katrina, Doherty, Daniel, Dorrani, Naghmeh, Doss, Argenia L., Douine, Emilie D., Earl, Dawn, Eckstein, David J., Emrick, Lisa T., Eng, Christine M., Falk, Marni, Fieg, Elizabeth L., Fisher, Paul G., Fogel, Brent L., Forghani, Irman, Gahl, William A., Glass, Ian, Gochuico, Bernadette, Goddard, Page C., Godfrey, Rena A., Grajewski, Alana, Hadley, Don, Halley, Meghan C., Hamid, Rizwan, Hassey, Kelly, Hayes, Nichole, High, Frances, Hing, Anne, Hisama, Fuki M., Holm, Ingrid A., Hom, Jason, Horike-Pyne, Martha, Huang, Alden, Hutchison, Sarah, Introne, Wendy, Isasi, Rosario, Izumi, Kosuke, Jarvik, Gail P., Jarvik, Jeffrey, Jayadev, Suman, Jean-Marie, Orpa, Jobanputra, Vaidehi, Kaitryn, Emerald, Ketkar, Shamika, Kiley, Dana, Kilich, Gonench, Kobren, Shilpa N., Kohane, Isaac S., Kohler, Jennefer N., Korrick, Susan, Krakow, Deborah, Krasnewich, Donna M., Kravets, Elijah, Lalani, Seema R., Lam, Byron, Lam, Christina, Lanpher, Brendan C., Lanza, Ian R., LeBlanc, Kimberly, Lee, Brendan H., Levitt, Roy, Lewis, Richard A., Liu, Pengfei, Liu, Xue Zhong, Longo, Nicola, Loo, Sandra K., Loscalzo, Joseph, Maas, Richard L., Macnamara, Ellen F., MacRae, Calum A., Maduro, Valerie V., Maghiro, Audrey Stephannie, Mahoney, Rachel, Malicdan, May Christine V., Mamounas, Laura A., Manolio, Teri A., Mao, Rong, Marom, Ronit, Marth, Gabor, Martin, Beth A., Martin, Martin G., Martínez-Agosto, Julian A., Marwaha, Shruti, McCauley, Jacob, McConkie-Rosell, Allyn, McCray, Alexa T., McGee, Elisabeth, Might, Matthew, Miller, Danny, Mirzaa, Ghayda, Moore, Ryan M., Morava, Eva, Moretti, Paolo, Mulvihill, John J., Nakano-Okuno, Mariko, Nelson, Stanley F., Nieves-Rodriguez, Shirley, Novacic, Donna, Oglesbee, Devin, Orengo, James P., Pace, Laura, Pak, Stephen, Pallais, J. Carl, Palmer, Christina G.S., Papp, Jeanette C., Parker, Neil H., Phillips, John A., Posey, Jennifer E., Potocki, Lorraine, Pusey Swerdzewski, Barbara N., Quinlan, Aaron, Rao, Deepak A., Raper, Anna, Raskind, Wendy, Renteria, Genecee, Reuter, Chloe M., Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Rosenfeld, Jill A., Rosenthal, Elizabeth, Rossignol, Francis, Ruzhnikov, Maura, Sacco, Ralph, Sampson, Jacinda B., Saporta, Mario, Schaechter, Judy, Schedl, Timothy, Schoch, Kelly, Scott, Daryl A., Seto, Elaine, Shashi, Vandana, Shelkowitz, Emily, Sheppeard, Sam, Shin, Jimann, Silverman, Edwin K., Sinsheimer, Janet S., Sisco, Kathy, Smith, Edward C., Smith, Kevin S., Solnica-Krezel, Lilianna, Solomon, Ben, Spillmann, Rebecca C., Stergachis, Andrew, Stoler, Joan M., Sullivan, Kathleen, Sullivan, Jennifer A., Sutton, Shirley, Sweetser, David A., Sybert, Virginia, Tabor, Holly K., Tan, Queenie K.-G., Tan, Amelia L.M., Tarakad, Arjun, Tekin, Mustafa, Telischi, Fred, Thorson, Willa, Tifft, Cynthia J., Toro, Camilo, Tran, Alyssa A., Ungar, Rachel A., Urv, Tiina K., Vanderver, Adeline, Velinder, Matt, Viskochil, Dave, Vogel, Tiphanie P., Wahl, Colleen E., Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Wan, Jijun, Wang, Lee-kai, Wangler, Michael F., Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wener, Mark, Wenger, Tara, Westerfield, Monte, Wheeler, Matthew T., Whitlock, Jordan, Wolfe, Lynne A., Worley, Kim, Xiao, Changrui, Yamamoto, Shinya, Yang, John, Zhang, Zhe, Zuchner, Stephan, Huang, Jing, Mignot, Cyril, Keren, Boris, Saillour, Virginie, Mah-Som, Annelise Y., Sacharow, Stephanie, Rajabi, Farrah, Costin, Carrie, Yamamoto, Shinya, Kanca, Oguz, Bellen, Hugo J., Rosenfeld, Jill A., Palmer, Christina G.S., Nelson, Stanley F., Wangler, Michael F., Martinez-Agosto, Julian A.

المصدر: Genetics in Medicine; November 2024, Vol. 26 Issue: 11

المؤلفون: Mulvihill, John J., Findley, Laura, Ni, Weihong, Sinsheimer, Janet S., Cole, F. Session, Esteves, Cecilia, Bernstein, Jonathan A., Newman, John H., Wheeler, Matthew T., Mokry, Jill R., Acosta, Maria T., Adams, David R., Afzali, Ben, Al-Beshri, Ali, Allworth, Aimee, Alvarez, Raquel L., Alvey, Justin, Andrews, Ashley, Ashley, Euan A., Bacino, Carlos A., Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bale, Jim, Bamshad, Michael, Barbouth, Deborah, Bayrak-Toydemir, Pinar, Beck, Anita, Beggs, Alan H., Behrens, Edward, Bejerano, Gill, Bellen, Hugo J., Bennett, Jimmy, Bernstein, Jonathan A., Berry, Gerard T., Bican, Anna, Bivona, Stephanie, Blue, Elizabeth, Bohnsack, John, Bonner, Devon, Borja, Nicholas, Botto, Lorenzo, Briere, Lauren C., Burke, Elizabeth A., Burrage, Lindsay C., Butte, Manish J., Byers, Peter, Byrd, William E., Callaway, Kaitlin, Carey, John, Carvalho, George, Cassini, Thomas, Chanprasert, Sirisak, Chao, Hsiao-Tuan, Chinn, Ivan, Clark, Gary D., Coakley, Terra R., Cobban, Laurel A., Cogan, Joy D., Coggins, Matthew, Cole, F. Sessions, Corner, Brian, Corona, Rosario I., Craigen, William J., Crouse, Andrew B., Cuddapah, Vishnu, Cunningham, Michael, D’Souza, Precilla, Dai, Hongzheng, Dasari, Surendra, Davis, Joie, Delgado, Margaret, Dell’Angelica, Esteban C., Dipple, Katrina, Doherty, Daniel, Dorrani, Naghmeh, Douglas, Jessica, Douine, Emilie D., Earl, Dawn, Emrick, Lisa T., Eng, Christine M., Ezell, Kimberly, Fieg, Elizabeth L., Fisher, Paul G., Fogel, Brent L., Fu, Jiayu, Gahl, William A., Ganetzky, Rebecca, Glanton, Emily, Glass, Ian, Goddard, Page C., Gonzalez, Joanna M., Gropman, Andrea, Halley, Meghan C., Hamid, Rizwan, Hanchard, Neal, Hassey, Kelly, Hayes, Nichole, High, Frances, Hing, Anne, Hisama, Fuki M., Holm, Ingrid A., Hom, Jason, Horike-Pyne, Martha, Huang, Alden, Huang, Yan, Hurst, Anna, Introne, Wendy, Jarvik, Gail P., Jarvik, Jeffrey, Jayadev, Suman, Marie, Orpa Jean-, Jobanputra, Vaidehi, Kaitryn, Emerald, Kanca, Oguz, Karasozen, Yigit, Ketkar, Shamika, Kiley, Dana, Kilich, Gonench, Kobren, Shilpa N., Kohane, Isaac S., Kohler, Jennefer N., Korf, Bruce, Korrick, Susan, Krakow, Deborah, Kravets, Elijah, Lalani, Seema R., Lam, Christina, Lanpher, Brendan C., Lanza, Ian R., Latchman, Kumarie, LeBlanc, Kimberly, Lee, Brendan H., Lewis, Richard A., Liu, Pengfei, Longo, Nicola, Loscalzo, Joseph, Maas, Richard L., Macnamara, Ellen F., MacRae, Calum A., Maduro, Valerie V., Maghiro, Audrey Stephannie, Mahoney, Rachel, Malicdan, May Christine V., Mao, Rong, Marom, Ronit, Marth, Gabor, Martin, Beth A., Martin, Martin G., Martínez-Agosto, Julian A., Marwaha, Shruti, McConkie-Rosell, Allyn, McCray, Alexa T., Might, Matthew, Mikati, Mohamad, Miller, Danny, Mirzaa, Ghayda, Morava, Eva, Moretti, Paolo, Morimoto, Marie, Mulvihill, John J., Nakano-Okuno, Mariko, Nelson, Stanley F., Neumann, Serena, Novacic, Donna, Oglesbee, Devin, Orengo, James P., Pace, Laura, Pak, Stephen, Pallais, J. Carl, Parker, Neil H., Peart, LéShon, Petcharet, Leoyklang, Phillips, John A., Posey, Jennifer E., Potocki, Lorraine, Pusey Swerdzewski, Barbara N., Quinlan, Aaron, Rajagopalan, Ramakrishnan, Rao, Deepak A., Raper, Anna, Raskind, Wendy, Rebelo, Adriana, Reuter, Chloe M., Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Rodriguez, Martin, Rosenfeld, Jill A., Rosenthal, Elizabeth, Rossignol, Francis, Ruzhnikov, Maura, Sabaii, Marla, Sampson, Jacinda B., Schedl, Timothy, Schoch, Kelly, Scott, Daryl A., Seto, Elaine, Shashi, Vandana, Shelkowitz, Emily, Sheppeard, Sam, Shin, Jimann, Silverman, Edwin K., Sisco, Kathy, Skelton, Tammi, Skraban, Cara, Smith, Carson A., Smith, Kevin S., Solnica-Krezel, Lilianna, Solomon, Ben, Spillmann, Rebecca C., Stergachis, Andrew, Stoler, Joan M., Sullivan, Kathleen, Sutton, Shirley, Sweetser, David A., Sybert, Virginia, Tabor, Holly K., Tan, Queenie K.-G., Tan, Amelia L.M., Tarakad, Arjun, Taylor, Herman, Tekin, Mustafa, Thorson, Willa, Tifft, Cynthia J., Toro, Camilo, Tran, Alyssa A., Ungar, Rachel A., Vanderver, Adeline, Velinder, Matt, Viskochil, Dave, Vogel, Tiphanie P., Wahl, Colleen E., Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Wangler, Michael F., Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wener, Mark, Wenger, Tara, Westerfield, Monte, Wheeler, Matthew T., Whitlock, Jordan, Wolfe, Lynne A., Wood, Heidi, Worley, Kim, Yamamoto, Shinya, Zhang, Zhe, Zuchner, Stephan

المصدر: Genetics in Medicine; October 2024, Vol. 26 Issue: 10