Pai Syndrome: Median Cleft Lip, Corpus Callosum Lipoma, and Fibroepithelial Skin Tag

von Azurdia, Jacob, Burke, Leah, Laub, Donald
Veröffentlicht 2014

Two Cases of Preaxial Polydactyly of the Foot: Important Implications for Plastic Surgeons

von Silverstein, Max L., Burke, Leah W., Laub, Donald R.
Veröffentlicht in Plast Reconstr Surg Glob Open (2021)

Glucan rich nutrition does not increase gut translocation of beta-glucan

von Hoenigl, Martin, Lin, John, Finkelman, Malcolm, Zhang, Yonglong, Karris, Maile Y., Letendre, Scott L., Ellis, Ronald J., Burke, Leah, Richard, Byron, Gaufin, Thaidra, Isnard, Stéphane, Routy, Jean-Pierre, Gianella, Sara
Veröffentlicht in Mycoses (2020)

Randomized Pilot Study of an Advanced Smart Pill Bottle as an Adherence Intervention in Patients with HIV on Antiretroviral Treatment

von Ellsworth, Grant B., Burke, Leah A., Wells, Martin T., Mishra, Satish, Caffrey, Matthew, Liddle, David, Madhava, Malika, O’Neal, Curtis, Anderson, Peter L., Bushman, Lane, Ellison, Lucas, Stein, Josh, Gulick, Roy M.
Veröffentlicht in J Acquir Immune Defic Syndr (2021)

Relationship between latent and rebound viruses in a clinical trial of anti–HIV-1 antibody 3BNC117

von Cohen, Yehuda Z., Lorenzi, Julio C.C., Krassnig, Lisa, Barton, John P., Burke, Leah, Pai, Joy, Lu, Ching-Lan, Mendoza, Pilar, Oliveira, Thiago Y., Sleckman, Christopher, Millard, Katrina, Butler, Allison L., Dizon, Juan P., Belblidia, Shiraz A., Witmer-Pack, Maggi, Shimeliovich, Irina, Gulick, Roy M., Seaman, Michael S., Jankovic, Mila, Caskey, Marina, Nussenzweig, Michel C.
Veröffentlicht in J Exp Med (2018)

The Undergraduate Training in Genomics (UTRIG) Initiative: early & active training for physicians in the genomic medicine era

von Wilcox, Rebecca L, Adem, Patricia V, Afshinnekoo, Ebrahim, Atkinson, James B, Burke, Leah W, Cheung, Hoiwan, Dasgupta, Shoumita, DeLaGarza, Julia, Joseph, Loren, LeGallo, Robin, Lew, Madelyn, Lockwood, Christina M, Meiss, Alice, Norman, Jennifer, Markwood, Priscilla, Rizvi, Hasan, Shane-Carson, Kate P, Sobel, Mark E, Suarez, Eric, Tafe, Laura J, Wang, Jason, Haspel, Richard L
Veröffentlicht in Per Med (2018)

3BNC117 a Broadly Neutralizing Antibody Suppresses Viremia in HIV-1-Infected Humans

von Caskey, Marina, Klein, Florian, Lorenzi, Julio C. C., Seaman, Michael S., West, Anthony P., Buckley, Noreen, Kremer, Gisela, Nogueira, Lilian, Braunschweig, Malte, Scheid, Johannes F., Horwitz, Joshua A., Shimeliovich, Irina, Ben Avraham-Shulman, Sivan, Witmer-Pack, Maggi, Platten, Martin, Lehmann, Clara, Burke, Leah A., Hawthorne, Thomas, Gorelick, Robert J., Walker, Bruce D., Keler, Tibor, Gulick, Roy M., Fätkenheuer, Gerd, Schlesinger, Sarah J., Nussenzweig, Michel C.
Veröffentlicht in Nature (2015)

HIV-1 antibody 3BNC117 suppresses viral rebound in humans during treatment interruption

von Scheid, Johannes F., Horwitz, Joshua A., Bar-On, Yotam, Kreider, Edward F., Lu, Ching-Lan, Lorenzi, Julio C. C., Feldmann, Anna, Braunschweig, Malte, Nogueira, Lilian, Oliveira, Thiago, Shimeliovich, Irina, Patel, Roshni, Burke, Leah, Cohen, Yehuda Z., Hadrigan, Sonya, Settler, Allison, Witmer-Pack, Maggi, West, Anthony P., Juelg, Boris, Keler, Tibor, Hawthorne, Thomas, Zingman, Barry, Gulick, Roy M., Pfeifer, Nico, Learn, Gerald H., Seaman, Michael S., Bjorkman, Pamela J., Klein, Florian, Schlesinger, Sarah J., Walker, Bruce D., Hahn, Beatrice H., Nussenzweig, Michel C., Caskey, Marina
Veröffentlicht in Nature (2016)

PIK3CA-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distribution

von Mirzaa, Ghayda, Timms, Andrew E., Conti, Valerio, Boyle, Evan August, Girisha, Katta M., Martin, Beth, Kircher, Martin, Olds, Carissa, Juusola, Jane, Collins, Sarah, Park, Kaylee, Carter, Melissa, Glass, Ian, Krägeloh-Mann, Inge, Chitayat, David, Parikh, Aditi Shah, Bradshaw, Rachael, Torti, Erin, Braddock, Stephen, Burke, Leah, Ghedia, Sondhya, Stephan, Mark, Stewart, Fiona, Prasad, Chitra, Napier, Melanie, Saitta, Sulagna, Straussberg, Rachel, Gabbett, Michael, O’Connor, Bridget C., Keegan, Catherine E., Yin, Lim Jiin, Lai, Angeline Hwei Meeng, Martin, Nicole, McKinnon, Margaret, Addor, Marie-Claude, Boccuto, Luigi, Schwartz, Charles E., Lanoel, Agustina, Conway, Robert L., Devriendt, Koenraad, Tatton-Brown, Katrina, Pierpont, Mary Ella, Painter, Michael, Worgan, Lisa, Reggin, James, Hennekam, Raoul, Tsuchiya, Karen, Pritchard, Colin C., Aracena, Mariana, Gripp, Karen W., Cordisco, Maria, Van Esch, Hilde, Garavelli, Livia, Curry, Cynthia, Goriely, Anne, Kayserilli, Hulya, Shendure, Jay, Graham, John, Guerrini, Renzo, Dobyns, William B.
Veröffentlicht in JCI Insight (2016)

Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation

von Koczkowska, Magdalena, Callens, Tom, Gomes, Alicia, Sharp, Angela, Chen, Yunjia, Hicks, Alesha D., Aylsworth, Arthur S., Azizi, Amedeo A., Basel, Donald G., Bellus, Gary, Bird, Lynne M., Blazo, Maria A., Burke, Leah W., Cannon, Ashley, Collins, Felicity, DeFilippo, Colette, Denayer, Ellen, Digilio, Maria C., Dills, Shelley K., Dosa, Laura, Greenwood, Robert S., Griffis, Cristin, Gupta, Punita, Hachen, Rachel K., Hernández-Chico, Concepción, Janssens, Sandra, Jones, Kristi J., Jordan, Justin T., Kannu, Peter, Korf, Bruce R., Lewis, Andrea M., Listernick, Robert H., Lonardo, Fortunato, Mahoney, Maurice J., Ojeda, Mayra Martinez, McDonald, Marie T., McDougall, Carey, Mendelsohn, Nancy, Miller, David T., Mori, Mari, Oostenbrink, Rianne, Perreault, Sebastién, Pierpont, Mary Ella, Piscopo, Carmelo, Pond, Dinel A., Randolph, Linda M., Rauen, Katherine A., Rednam, Surya, Rutledge, S. Lane, Saletti, Veronica, Schaefer, G. Bradley, Schorry, Elizabeth K., Scott, Daryl A., Shugar, Andrea, Siqveland, Elizabeth, Starr, Lois J., Syed, Ashraf, Trapane, Pamela L., Ullrich, Nicole J., Wakefield, Emily G., Walsh, Laurence E., Wangler, Michael F., Zackai, Elaine, Claes, Kathleen B. M., Wimmer, Katharina, van Minkelen, Rick, De Luca, Alessandro, Martin, Yolanda, Legius, Eric, Messiaen, Ludwine M.
Veröffentlicht in Genet Med (2018)

Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation

von Koczkowska, Magdalena, Callens, Tom, Gomes, Alicia, Sharp, Angela, Chen, Yunjia, Hicks, Alesha D., Aylsworth, Arthur S., Azizi, Amedeo A., Basel, Donald G., Bellus, Gary, Bird, Lynne M., Blazo, Maria A., Burke, Leah W., Cannon, Ashley, Collins, Felicity, DeFilippo, Colette, Denayer, Ellen, Digilio, Maria C., Dills, Shelley K., Dosa, Laura, Greenwood, Robert S., Griffis, Cristin, Gupta, Punita, Hachen, Rachel K., Hernández-Chico, Concepción, Janssens, Sandra, Jones, Kristi J., Jordan, Justin T., Kannu, Peter, Korf, Bruce R., Lewis, Andrea M., Listernick, Robert H., Lonardo, Fortunato, Mahoney, Maurice J., Ojeda, Mayra Martinez, McDonald, Marie T., McDougall, Carey, Mendelsohn, Nancy, Miller, David T., Mori, Mari, Oostenbrink, Rianne, Perreault, Sebastién, Pierpont, Mary Ella, Piscopo, Carmelo, Pond, Dinel A., Randolph, Linda M., Rauen, Katherine A., Rednam, Surya, Rutledge, S. Lane, Saletti, Veronica, Schaefer, G. Bradley, Schorry, Elizabeth K., Scott, Daryl A., Shugar, Andrea, Siqveland, Elizabeth, Starr, Lois J., Syed, Ashraf, Trapane, Pamela L., Ullrich, Nicole J., Wakefield, Emily G., Walsh, Laurence E., Wangler, Michael F., Zackai, Elaine, Claes, Kathleen B. M., Wimmer, Katharina, van Minkelen, Rick, De Luca, Alessandro, Martin, Yolanda, Legius, Eric, Messiaen, Ludwine M.
Veröffentlicht in Genet Med (2018)