Employing effective recruitment and retention strategies to engage a diverse pediatric population in genomics research

Authors: Ramos, Michelle A., Bonini, Katherine E., Scarimbolo, Laura, Kelly, Nicole R., Insel, Beverly, Suckiel, Sabrina A., Brown, Kaitlyn, Di Biase, Miranda, Gallagher, Katie M., Lopez, Jessenia, Aguiñiga, Karla López, Marathe, Priya N., Maria, Estefany, Odgis, Jacqueline A., Rodriguez, Jessica E., Rodriguez, Michelle A., Ruiz, Nairovylex, Sebastin, Monisha, Yelton, Nicole M., Cunningham-Rundles, Charlotte, Gertner, Melvin, Laguerre, Irma, McDonald, Thomas V., McGoldrick, Patricia E., Robinson, Mimsie, Rubinstein, Arye, Shulman, Lisa H., Williams, Trinisha, Wolf, Steven M., Yozawitz, Elissa G., Zinberg, Randi E., Abul-Husn, Noura S., Bauman, Laurie J., Diaz, George A., Ferket, Bart S., Greally, John M., Jobanputra, Vaidehi, Gelb, Bruce D., Kenny, Eimear E., Wasserstein, Melissa P., Horowitz, Carol R.

Source: In The American Journal of Human Genetics 5 December 2024 111(12):2607-2617

Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual population

Authors: Marathe, Priya N., Suckiel, Sabrina A., Bonini, Katherine E., Kelly, Nicole R., Scarimbolo, Laura, Insel, Beverly J., Odgis, Jacqueline A., Sebastin, Monisha, Ramos, Michelle A., Di Biase, Miranda, Gallagher, Katie M., Brown, Kaitlyn, Rodriguez, Jessica E., Yelton, Nicole, Aguiñiga, Karla Lopez, Rodriguez, Michelle A., Maria, Estefany, Lopez, Jessenia, Zinberg, Randi E., Diaz, George A., Greally, John M., Abul-Husn, Noura S., Bauman, Laurie J., Gelb, Bruce D., Wasserstein, Melissa P., Kenny, Eimear E., Horowitz, Carol R.

Source: In Human Genetics and Genomics Advances 18 July 2024 5(3)

Physician services and costs after disclosure of diagnostic sequencing results in the NYCKidSeq program

Authors: Berkalieva, Asem, Kelly, Nicole R., Fisher, Ashley, Hohmann, Samuel F., Sebastin, Monisha, Di Biase, Miranda, Bonini, Katherine E., Marathe, Priya, Odgis, Jacqueline A., Suckiel, Sabrina A., Ramos, Michelle A., Rhodes, Rosamond, Abul-Husn, Noura S., Greally, John M., Horowitz, Carol R., Wasserstein, Melissa P., Kenny, Eimear E., Gelb, Bruce D., Ferket, Bart S.

Source: In Genetics in Medicine January 2024 26(1)

Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program

Authors: Bonini, Katherine E., Thomas‐Wilson, Amanda, Marathe, Priya N., Sebastin, Monisha, Odgis, Jacqueline A., Di Biase, Miranda, Kelly, Nicole R., Ramos, Michelle A., Insel, Beverly J., Scarimbolo, Laura, Rehman, Atteeq U., Guha, Saurav, Okur, Volkan, Abhyankar, Avinash, Phadke, Shruti, Nava, Caroline, Gallagher, Katie M., Elkhoury, Lama, Edelmann, Lisa, Zinberg, Randi E., Abul‐Husn, Noura S., Diaz, George A., Greally, John M., Suckiel, Sabrina A., Horowitz, Carol R., Kenny, Eimear E., Wasserstein, Melissa, Gelb, Bruce D., Jobanputra, Vaidehi

Source: Clinical genetics. 104(2):210-225

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100189647741.0x000001&indx=1&recIds=ETOCvdc_100189647741.0x000001

Detection of mosaic variants using genome sequencing in a large pediatric cohort

Authors: Odgis, Jacqueline A., Gallagher, Katie M., Rehman, Atteeq U., Marathe, Priya N., Bonini, Katherine E., Sebastin, Monisha, Di Biase, Miranda, Brown, Kaitlyn, Kelly, Nicole R., Ramos, Michelle A., Thomas‐Wilson, Amanda, Guha, Saurav, Okur, Volkan, Ganapathi, Mythily, Elkhoury, Lama, Edelmann, Lisa, Zinberg, Randi E., Abul‐Husn, Noura S., Diaz, George A., Greally, John M., Suckiel, Sabrina A., Jobanputra, Vaidehi, Horowitz, Carol R., Kenny, Eimear E., Wasserstein, Melissa P., Gelb, Bruce D.

Source: American journal of medical genetics.Part A. 191(3):699-710

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100173598961.0x000001&indx=1&recIds=ETOCvdc_100173598961.0x000001

Conducting clinical genomics research during the COVID‐19 pandemic: Lessons learned from the CSER consortium experience

Authors: Kraft, Stephanie A., Russell, Heidi, Bensen, Jeannette T., Bonini, Katherine E., Robinson, Jill O., Sahin‐Hodoglugil, Nuriye, Renna, Kathleen, Hindorff, Lucia A., Kaufman, Dave, Horowitz, Carol R., Waltz, Margaret, Zepp, Jamilyn M., Knight, Sara J.

Source: American journal of medical genetics.Part A. 191(2):391-399

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100170804772.0x000001&indx=1&recIds=ETOCvdc_100170804772.0x000001

The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic results disclosure in diverse families

Authors: Suckiel, Sabrina A., Kelly, Nicole R., Odgis, Jacqueline A., Gallagher, Katie M., Sebastin, Monisha, Bonini, Katherine E., Marathe, Priya N., Brown, Kaitlyn, Di Biase, Miranda, Ramos, Michelle A., Rodriguez, Jessica E., Scarimbolo, Laura, Insel, Beverly J., Ferar, Kathleen D.M., Zinberg, Randi E., Diaz, George A., Greally, John M., Abul-Husn, Noura S., Bauman, Laurie J., Gelb, Bruce D., Horowitz, Carol R., Wasserstein, Melissa P., Kenny, Eimear E.

Source: In The American Journal of Human Genetics 7 December 2023 110(12):2029-2041

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

Authors: Abul-Husn, Noura S., Marathe, Priya N., Kelly, Nicole R., Bonini, Katherine E., Sebastin, Monisha, Odgis, Jacqueline A., Abhyankar, Avinash, Brown, Kaitlyn, Di Biase, Miranda, Gallagher, Katie M., Guha, Saurav, Ioele, Nicolette, Okur, Volkan, Ramos, Michelle A., Rodriguez, Jessica E., Rehman, Atteeq U., Thomas-Wilson, Amanda, Edelmann, Lisa, Zinberg, Randi E., Diaz, George A., Greally, John M., Jobanputra, Vaidehi, Suckiel, Sabrina A., Horowitz, Carol R., Wasserstein, Melissa P., Kenny, Eimear E., Gelb, Bruce D.

Source: In Genetics in Medicine September 2023 25(9)

Information-seeking preferences in diverse patients receiving a genetic testing result in the Clinical Sequencing Evidence-Generating Research (CSER) study

Authors: Slavotinek, Anne, Prasad, Hannah, Outram, Simon, Scollon, Sarah, Rego, Shannon, Yip, Tiffany, Hoban, Hannah, Foreman, Kate M., Kelley, Whitley, Finnila, Candice, Berg, Jonathan, Murali, Priyanka, Bonini, Katherine E., Martin, Lisa J., Hott, Adam

Source: In Genetics in Medicine September 2023 25(9)

Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testing

Authors: Felker, Stephanie A., Lawlor, James M.J., Hiatt, Susan M., Thompson, Michelle L., Latner, Donald R., Finnila, Candice R., Bowling, Kevin M., Bonnstetter, Zachary T., Bonini, Katherine E., Kelly, Nicole R., Kelley, Whitley V., Hurst, Anna C.E., Rashid, Salman, Kelly, Melissa A., Nakouzi, Ghunwa, Hendon, Laura G., Bebin, E. Martina, Kenny, Eimear E., Cooper, Gregory M.

Source: In Genetics in Medicine August 2023 25(8)

Returning integrated genomic risk and clinical recommendations: The eMERGE study

Authors: Gordon, Adam, Sobowale, Agboade, Allworth, Aimee, Patel, Akshar, DiVietro, Alanna, Strong, Alanna, Sherafati, Alborz, Sherfati, Alborz, Bick, Alex, Miller, Alexandra, Chandel, Alka, Rosenthal, Alyssa, Khera, Amit, Kontorovich, Amy, Beck, Andrew, Beck, Andy, Espinoza, Angelica, Lewis, Anna, Prince, Anya, Khan, Atlas, Iverson, Ayuko, Khales, Bahram Namjou, Benoit, Barbara, Hernan, Becca, Kallman, Ben, Kerman, Ben, Shoemaker, Ben, Satterfield, Benjamin, Devine, Beth, Etheridge, Bethany, Goff, Blake, Freimuth, Bob, Grundmeier, Bob, Collier, Brenae, Mutai, Brenda, Harnett, Brett, Chang, Brian, Piening, Brian, Davis, Brittney, Korf, Bruce, Patterson, Candace, Demetriou, Carmen, Ta, Casey, Hammack, Catherine, Nelson, Catrina, Gascoigne, Caytie, Dorn, Chad, Moretz, Chad, Kachulis, Chris, Hoell, Christie, Cowles, Christine, Lange, Christoph, Weng, Chunhua, Prows, Cindy, Brokamp, Cole, Liu, Cong, Scherr, Courtney, Gonzalez, Crystal, Ramirez, Cynthia, Shimbo, Daichi, Roden, Dan, Schaid, Daniel, Kaufman, Dave, Crosslin, David, Kochan, David, Veenstra, David, Singh, Davinder, Karavite, Dean, Abrams, Debbie, Absher, Devin, Edwards, Digna Velez, Haverfield, Eden, Morales, Eduardo, Esplin, Edward, Malolepsza, Edyta, Alipour, Ehsan, Kenny, Eimear, Rosenthal, Elisabeth, Duvall, Eliza, McNally, Elizabeth, Bhoj, Elizabeth, Cohn, Elizabeth, Hibler, Elizabeth, Karlson, Elizabeth, Clayton, Ellen, Chesnut, Emily, DeFranco, Emily, Gallagher, Emily, Soper, Emily, Perez, Emma, Cash, Erin, Berner, Eta, Wang, Fei, Wehbe, Firas, Ricci, Francisco, Mentch, Frank, Shaibi, Gabriel, Jarvik, Gail, Hahn, George, Hripcsak, George, Wiesner, Georgia, Belbin, Gillian, Davogustto, Gio, Nadkarni, Girish, Qiu, Haijun, Hakonarson, Hakon, Bangash, Hana, Beasley, Hannah, Liu, Hao, Aungst, Heide, Tiwari, Hemant, Duckham, Hillary, Thomas, Hope, Kullo, Iftikhar, Holm, Ingrid, Allen, Isabelle, Ionita-Laza, Iuliana, Hellwege, Jacklyn, Petrzelka, Jacob, Odgis, Jacqueline, Narula, Jahnavi, Petrzelka, Jake, Patel, Jalpa, Cimino, James, Meigs, James, Snyder, James, Olson, Janet, Zahner, Janet, Pennington, Jeff, Pacheco, Jen, Pacheco, Jennifer Allen, Morse, Jennifer, Corsmo, Jeremy, Thayer, Jeritt, Cimino, Jim, Chen, Jingheng, Fournier, Jocelyn, Jackson, Jodell, Glessner, Joe, Pacyna, Joel, Smith, Johanna, Connolly, John, Lynch, John, Shelley, John, Mosley, Jonathan, Nestor, Jordan, Smoller, Jordan, Alsip, Jorge, Kannry, Joseph, Sutton, Joseph, Peterson, Josh, Smith, Joshua, Galasso, Julia, Smith, Julia, Wynn, Julia, Gundelach, Justin, Starren, Justin, Choi, Karmel, Mittendorf, Kate, Anderson, Katherine, Bonini, Katherine, Leppig, Kathleen, Muenzen, Kathleen, Larkin, Katie, Stuttgen, Kelsey, Wiley, Ken, Nguyen, Kenny, Dufendach, Kevin, Atkins, Kiley, Sawicki, Konrad, Norland, Kristjan, Kiryluk, Krzysztof, Beskow, Laura, Rasmussen-Torvik, Laura, Kottyan, Leah, Hsu, Li, Tian, Lifeng, Mahanta, Lisa, Martin, Lisa, Wang, Lisa, Gomez, Lizbeth, Thompson, Lorenzo, Orlando, Lori, Richter, Lucas, Rasmussen, Luke, Petukhova, Lynn, Seabolt, Lynn, O’Brien, Madison, Harden, Maegan, Fullerton, Malia, Harr, Margaret, Beasley, Mark, Guindo, Marta, Horike, Martha, Horike-Pyne, Martha, Abdalla, Marwah, Hamed, Marwan, Terry, Mary Beth, Maradik, Mary, Wyatt, Matt, Davis, Matthew, Lebo, Matthew, Smith, Maureen, Rosario, Maya del, Sabatello, Maya, Behr, Meckenzie, Roy-Puckelwartz, Meg, Habrat, Mel, Myers, Melanie, Yetisgen, Meliha, Iris, Merve, DaSilva, Michael, Preuss, Michael, McGowan, Michelle, Shi, Mingjian, Perera, Minoli, Thomas, Minta, Elkind, Mitch, Abbass, Mohammad, Saadatagah, Mohammad, Hess, Molly, Maradik, Molly, Vaitinadin, Nataraja “RJ”, Vaitinadin, Nataraja, Muthu, Naveen, Netherly, Neil, Lennon, Niall, Shang, Ning, Limdi, Nita, Forrest, Noah, Romero, Noheli, Robinson, Nora, Abul-Husn, Noura, Elsekaily, Omar, Dikilitas, Ozan, Kovatch, Patricia, Davis, Patrick, Appelbaum, Paul, Francaviglia, Paul, O’Reilly, Paul, Chandler, Paulette, Caraballo, Pedro, Tarczy-Hornoch, Peter, Shum, Pierre, Marathe, Priya, Murali, Priyanka, Feng, Qiping, Wells, Quinn, Atchley, Rachel, Narla, Radhika, Barton, Rene, Sterling, Rene, Chisholm, Rex, Green, Richard, Sharp, Richard, Peters, Riki, Kukafka, Rita, Rowley, Robb, Freimuth, Robert, Green, Robert, Winter, Robert, Mueller, Roger, Loos, Ruth, Irvin, Ryan, Suckiel, Sabrina, Hussain, Sajjad, Sharba, Samer, Aronson, Sandy, Jones, Sarah, Knerr, Sarah, Nigbur, Scott, Weiss, Scott, Mooney, Sean, Terek, Shannon, Aufox, Sharon, Nirenberg, Sharon, Murphy, Shawn, O’Byrne, Sheila, Wang (Sam) Choi, Shing, Aguilar, Sienna, Bland, S.T., Rodrigues, Stefanie, Ledbetter, Stephanie, Rutledge, Stephanie, Booth, Stuart James, Xian, Su, Trinidad, Susan Brown, Bakken, Suzanne, Schmidlen, Tara, Rakhra-Burris, Tejinder, Manolio, Teri, Mersha, Tesfaye, Walunas, Theresa, Chandereng, Thevaa, May, Thomas, Ge, Tian, Edwards, Todd, Kaszemacher, Tom, Hernandez, Valentina, Willis, Valerie, Desai, Vemi, Desai, Vimi, Lorenzi, Virginia, Gainer, Vivian, Wei, Wei-Qi, Chung, Wendy, Su, Wu-Chen, Chang, Xiao, Zhao, Yiqing, Luo, Yuan, Shen, Yufeng, Linder, Jodell E., Bland, Harris T., Caraballo, Pedro J., Chisholm, Rex L., Clayton, Ellen Wright, Crosslin, David R., Esplin, Edward D., Forman, Sophie, Freimuth, Robert R., Gordon, Adam S., 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., Prows, Cynthia A., Rasmussen, Luke V., Sawicki, Konrad Teodor, Velez Edwards, Digna R., Abul-Husn, Noura S., Below, Jennifer E., Berner, Eta S., Booth, James, Chung, Wendy K., Cimino, James J., Fullerton, Stephanie M., Guiducci, Candace, Habrat, Melissa L., Hain, Heather, Hoell, Christin, Irvin, Marguerite R., Kachulis, Christopher, Kenny, Eimear E., Kullo, Iftikhar J., Manolio, Teri A., McNally, Elizabeth M., Mooney, Sean D., Namjou, Bahram, Perez, Emma F., Puckelwartz, Megan J., Roden, Dan M., Rosenthal, Elisabeth A., Saadatagah, Seyedmohammad, Schaid, Dan J., Schultz, Baergen, Shaibi, Gabriel Q., Sharp, Richard R., Shirts, Brian, Smith, Maureen E., Smoller, Jordan W., Suckiel, Sabrina A., Tiwari, Hemant K., Trinidad, Susan B., Wells, Quinn S., Wiesner, Georgia L., Peterson, Josh F.

Source: In Genetics in Medicine April 2023 25(4)

Perspectives of diverse Spanish- and English-speaking patients on the clinical use of polygenic risk scores

Authors: Suckiel, Sabrina A., Braganza, Giovanna T., Aguiñiga, Karla López, Odgis, Jacqueline A., Bonini, Katherine E., Kenny, Eimear E., Hamilton, Jada G., Abul-Husn, Noura S.

Source: In Genetics in Medicine June 2022 24(6):1217-1226

Modern Family: An Ethical Justification for System-Led Contact of Relatives Eligible for Cascade Screening in the United States.

Authors: Bonini, Katherine E.¹ (AUTHOR), Smith, Hadley Stevens^2,3 (AUTHOR), Bonkowski, Emily S.^4,5 (AUTHOR), Berkman, Benjamin E.^6,7 (AUTHOR), Jamal, Leila^6,8 (AUTHOR) leila.jamal@nih.gov

Source: Public Health Genomics. Nov2024, Vol. 28 Issue 1, p19-33. 15p. 1 Illustration.

Subject Terms: *PUBLIC health ethics, *GENETIC testing, *HEALTH facilities, *HOSPITAL administrators, *MEDICAL screening

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P318: Impact of genetic counseling using GUÍA on diverse families’ understanding of genomic results: Finding from the NYCKidSeq randomized controlled trial*

Authors: Suckiel, Sabrina, Kelly, Nicole, Odgis, Jacqueline, Gallagher, Katie, Sebastin, Monisha, Bonini, Katherine, Marathe, Priya, Brown, Kaitlyn, Di Biase, Miranda, Ramos, Michelle, Rodriguez, Jessica, Scarimbolo, Laura, Insel, Beverly, Zinberg, Randi, Diaz, George, Greally, John, Abul-Husn, Noura, Bauman, Laurie, Horowitz, Carol, Gelb, Bruce, Wasserstein, Melissa, Kenny, Eimear

Source: In Genetics in Medicine Open 2023 1(1) Supplement

P245: GUÍA application: Effectiveness in enhancing communication of genomic results in diverse, multilingual populations*

Authors: Marathe, Priya, Suckiel, Sabrina, Odgis, Jacqueline, Gallagher, Katie, Sebastin, Monisha, Bonini, Katherine, Brown, Kaitlyn, Di Biase, Miranda, Kelly, Nicole, Ramos, Michelle, Rodriguez, Jessica, Scarimbolo, Laura, Insel, Beverly, Zinberg, Randi, Diaz, George, Greally, John, Abul-Husn, Noura, Bauman, Laurie, Horowitz, Carol, Gelb, Bruce, Wasserstein, Melissa, Kenny, Eimear

Source: In Genetics in Medicine Open 2023 1(1) Supplement

The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing.

Authors: Sebastin, Monisha, Odgis, Jacqueline A., Suckiel, Sabrina A., Bonini, Katherine E., Di Biase, Miranda, Brown, Kaitlyn, Marathe, Priya, Kelly, Nicole R., Ramos, Michelle A., Rodriguez, Jessica E., Aguiñiga, Karla López, Lopez, Jessenia, Maria, Estefany, Rodriguez, Michelle A., Yelton, Nicole M., Cunningham-Rundles, Charlotte, Gallagher, Katie, McDonald, Thomas V., McGoldrick, Patricia E., Robinson, Mimsie

Source: Pilot & Feasibility Studies; 3/22/2023, Vol. 9 Issue 1, p1-13, 13p

Subject Terms: WHOLE genome sequencing, NUCLEOTIDE sequencing, MEDICALLY underserved persons, CHILD care, TELEMEDICINE, GENETIC counseling

Geographic Terms: NEW York (N.Y.), NEW York (State)

eP236: TeleKidSeq: Incorporating telehealth into clinical care of children from diverse backgrounds undergoing clinical genome sequencing

Authors: Sebastin, Monisha, Odgis, Jacqueline, Suckiel, Sabrina, Bonini, Katherine, Di Biase, Miranda, Brown, Kaitlyn, Marathe, Priya, Kelly, Nicole, Ramos, Michelle, Rodriguez, Jessica, Aguiniga, Karla Lopez, Lopez, Jessenia, Maria, Estefany, Rodriguez, Michelle, Yelton, Nicole, Cunningham-Rundles, Charlotte, Gallagher, Katie, McDonald, Thomas, McGoldrick, Patricia, Robinson, Mimsie, Rubinstein, Arye, Shulman, Lisa, Wolf, Steven, Yozawitz, Elissa, Zinberg, Randi, Abul-Husn, Noura, Bauman, Laurie, Diaz, George, Ferket, Bart, Greally, John, Jobanputra, Vaidehi, Gelb, Bruce, Horowitz, Carol, Kenny, Eimear, Wasserstein, Melissa

Source: In Genetics in Medicine March 2022 24(3) Supplement:S150-S150

Experiences of genetic counselors in referring young and metastatic breast cancer patients to support services: A needs assessment.

Authors: Clark, Elizabeth Bourquardez¹ (AUTHOR), Bonini, Katherine E.^1,2 (AUTHOR), Pugh Yi, Robin H.³ (AUTHOR), Kuhn, Erica⁴ (AUTHOR), Klemp, Jennifer R.^5,6 (AUTHOR), Rose, Diane⁷ (AUTHOR), Owens, Kelly N.⁷ (AUTHOR), Welcsh, Piri L.⁷ (AUTHOR), Conaty, Jessica⁸ (AUTHOR), Duquette, Debra⁹ (AUTHOR), Friedman, Susan J.⁷ (AUTHOR), Dean, Marleah^1,10 (AUTHOR) marleahdeank@usf.edu

Source: Patient Education & Counseling. Nov2023, Vol. 116, pN.PAG-N.PAG. 1p.

Subject Terms: *METASTATIC breast cancer, *SERVICES for cancer patients, *NEEDS assessment, *MEDICAL personnel, *SUPPORT services (Education), *SEXUAL health

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

Authors: Abul-Husn, Noura S., Marathe, Priya N., Kelly, Nicole R., Bonini, Katherine E., Sebastin, Monisha, Odgis, Jacqueline A., Abhyankar, Avinash, Brown, Kaitlyn, Di Biase, Miranda, Gallagher, Katie M., Guha, Saurav, Ioele, Nicolette, Okur, Volkan, Ramos, Michelle A., Rodriguez, Jessica E., Rehman, Atteeq U., Thomas-Wilson, Amanda, Edelmann, Lisa, Zinberg, Randi E., Diaz, George A., Greally, John M., Jobanputra, Vaidehi, Suckiel, Sabrina A., Horowitz, Carol R., Wasserstein, Melissa P., Kenny, Eimear E., Gelb, Bruce D.

Source: Genetics in Medicine; 20240101, Issue: Preprints