Fetal therapies and trials for lysosomal storage diseases: a survey of attitudes of parents and patients

por Schwab, Marisa E., Brown, Julia E. H., Lianoglou, Billie, Jin, Chengshi, Conroy, Patricia C., Gallagher, Renata C., Harmatz, Paul, MacKenzie, Tippi C.
Publicado 2022

“Let’s Just Wait Until She’s Born”: Temporal Factors That Shape Decision-Making for Prenatal Genomic Sequencing Amongst Families Underrepresented in Genomic Research

por Brown, Julia E. H., Zamora, Astrid N., Outram, Simon, Sparks, Teresa N., Lianoglou, Billie R., Norstad, Matthew, Sahin Hodoglugil, Nuriye N., Norton, Mary E., Ackerman, Sara L.
Publicado 2022

Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium

por Suckiel, Sabrina A., O’Daniel, Julianne M., Donohue, Katherine E., Gallagher, Katie M., Gilmore, Marian J., Hendon, Laura G., Joseph, Galen, Lianoglou, Billie R., Mathews, Jennifer M., Norton, Mary E., Odgis, Jacqueline A., Poss, Alexis F., Rego, Shannon, Scollon, Sarah, Yip, Tiffany, Amendola, Laura M.
Publicado 2021

Consensus statement for the perinatal management of patients with α thalassemia major

por MacKenzie, Tippi C., Amid, Ali, Angastiniotis, Michael, Butler, Craig, Gilbert, Sandra, Gonzalez, Juan, Keller, Roberta L., Kharbanda, Sandhya, Kirby-Allen, Melanie, Koenig, Barbara A., Kyono, Wade, Lal, Ashutosh, Lianoglou, Billie R., Norton, Mary E., Ogasawara, Keith K., Panchalee, Tachjaree, Rosner, Mara, Schwab, Marisa, Thompson, Alexis, Waye, John S., Vichinsky, Elliott
Publicado 2021

Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population

por Slavotinek, Anne, Rego, Shannon, Sahin-Hodoglugil, Nuriye, Kvale, Mark, Lianoglou, Billie, Yip, Tiffany, Hoban, Hannah, Outram, Simon, Anguiano, Beatrice, Chen, Flavia, Michelson, Jeremy, Cilio, Roberta M., Curry, Cynthia, Gallagher, Renata C., Gardner, Marisa, Kuperman, Rachel, Mendelsohn, Bryce, Sherr, Elliott, Shieh, Joseph, Strober, Jonathan, Tam, Allison, Tenney, Jessica, Weiss, William, Whittle, Amy, Chin, Garrett, Faubel, Amanda, Prasad, Hannah, Mavura, Yusuph, Van Ziffle, Jessica, Devine, W. Patrick, Hodoglugil, Ugur, Martin, Pierre-Marie, Sparks, Teresa N., Koenig, Barbara, Ackerman, Sara, Risch, Neil, Kwok, Pui-Yan, Norton, Mary E.
Publicado 2023

Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population

por Slavotinek, Anne, Rego, Shannon, Sahin-Hodoglugil, Nuriye, Kvale, Mark, Lianoglou, Billie, Yip, Tiffany, Hoban, Hannah, Outram, Simon, Anguiano, Beatrice, Chen, Flavia, Michelson, Jeremy, Cilio, Roberta M., Curry, Cynthia, Gallagher, Renata C., Gardner, Marisa, Kuperman, Rachel, Mendelsohn, Bryce, Sherr, Elliott, Shieh, Joseph, Strober, Jonathan, Tam, Allison, Tenney, Jessica, Weiss, William, Whittle, Amy, Chin, Garrett, Faubel, Amanda, Prasad, Hannah, Mavura, Yusuph, Van Ziffle, Jessica, Devine, W. Patrick, Hodoglugil, Ugur, Martin, Pierre-Marie, Sparks, Teresa N., Koenig, Barbara, Ackerman, Sara, Risch, Neil, Kwok, Pui-Yan, Norton, Mary E.
Publicado 2023

The impact of in utero transfusions on perinatal outcomes in patients with alpha thalassemia major: the UCSF registry

por Schwab, Marisa E., Lianoglou, Billie R., Gano, Dawn, Gonzalez Velez, Juan, Allen, Isabel E., Arvon, Regina, Baschat, Ahmet, Bianchi, Diana W., Bitanga, Melissa, Bourguignon, Anne, Brown, Richard N., Chen, Bruce, Chien, May, Davis-Nelson, Shareece, de Laat, Monique W.M., Ekwattanakit, Supachai, Gollin, Yvonne, Hirata, Greigh, Jelin, Angie, Jolley, Jennifer, Meyer, Paul, Miller, Jena, Norton, Mary E., Ogasawara, Keith K., Panchalee, Tachjaree, Schindewolf, Erica, Shaw, Steven W., Stumbaugh, Tammy, Thompson, Alexis A., Towner, Dena, Tsai, Pai-Jong Stacy, Viprakasit, Vip, Volanakis, Emmanuel, Zhang, Li, Vichinsky, Elliott, MacKenzie, Tippi C.
Publicado 2022