Systems pharmacology and genome medicine: a future perspective

por Wist, Aislyn D, Berger, Seth I, Iyengar, Ravi
Publicado 2009

Genes2Networks: connecting lists of gene symbols using mammalian protein interactions databases

por Berger, Seth I, Posner, Jeremy M, Ma'ayan, Avi
Publicado 2007

Systematic analysis of the effect of multiple templates on the accuracy of comparative models of protein structure

por Chakravarty, Suvobrata, Godbole, Sucheta, Zhang, Bing, Berger, Seth, Sanchez, Roberto
Publicado 2008

Unexplained oral and extremity ulcerations in an infant

por Russomanno, Kristen, DiLorenzo, Ashley, Simpson, Kara, Berger, Seth, Habeshian, Kaiane
Publicado 2021

A Systematic Review of Monogenic Etiologies of Nonimmune Hydrops Fetalis

por Quinn, Andrea M., Valcarcel, Breanna N., Makhamreh, Mona M., Al-Kouatly, Huda B., Berger, Seth I.
Publicado 2020

SNAVI: Desktop application for analysis and visualization of large-scale signaling networks

por Ma'ayan, Avi, Jenkins, Sherry L, Webb, Ryan L, Berger, Seth I, Purushothaman, Sudarshan P, Abul-Husn, Noura S, Posner, Jeremy M, Flores, Tony, Iyengar, Ravi
Publicado 2009

Genomic and biochemical analysis of repeatedly observed variants in DBT in individuals with maple syrup urine disease of Central American ancestry

por Billington, Charles J., Chapman, Kimberly A., Leon, Eyby, Meltzer, Beatrix W., Berger, Seth I., Olson, Matthew, Figler, Robert A., Hoang, Steve A., Wanxing, Cui, Wamhoff, Brian R., Collado, M. Sol, Cusmano‐Ozog, Kristina
Publicado 2022

“Development and Implementation of Novel Chatbot-based Genomic Research Consent”

por Smith, Erica D., Savage, Sarah K., Andrew, E. Hallie, Martin, Gloria Mas, Kahn-Kirby, Amanda H., LoTempio, Jonathan, Délot, Emmanuèle, Cohen, Andrea J., Pitsava, Georgia, Berger, Seth, Fusaro, Vincent A., Vilain, Eric
Publicado 2023

Somatic Mosaicism of IDH1 R132H Predisposes to Anaplastic Astrocytoma: A Case of Two Siblings

por Lee, Sulgi, Kambhampati, Madhuri, Almira-Suarez, M. Isabel, Ho, Cheng-Ying, Panditharatna, Eshini, Berger, Seth I., Turner, Joyce, Van Mater, David, Kilburn, Lindsay, Packer, Roger J., Myseros, John S., Vilain, Eric, Nazarian, Javad, Bornhorst, Miriam
Publicado 2020

Beyond the exome: what’s next in diagnostic testing for Mendelian conditions

por Wojcik, Monica H., Reuter, Chloe M., Marwaha, Shruti, Mahmoud, Medhat, Duyzend, Michael H., Barseghyan, Hayk, Yuan, Bo, Boone, Philip M., Groopman, Emily E., Délot, Emmanuèle C., Jain, Deepti, Sanchis-Juan, Alba, Starita, Lea M., Talkowski, Michael, Montgomery, Stephen B., Bamshad, Michael J., Chong, Jessica X., Wheeler, Matthew T., Berger, Seth I., O’Donnell-Luria, Anne, Sedlazeck, Fritz J., Miller, Danny E.
Publicado 2023

Defining the clinical phenotype of Saul-Wilson syndrome.

por Ferreira, Carlos R., Zein, Wadih M., Huryn, Laryssa A., Merker, Andrea, Berger, Seth I., Wilson, William G., Tiller, George E., Wolfe, Lynne A., Merideth, Melissa, Carvalho, Daniel R., Duker, Angela L., Bratke, Heiko, Haug, Marte Gjøl, Rohena, Luis, Hove, Hanne B., Xia, Zhi-Jie, Ng, Bobby G., Freeze, Hudson H., Gabriel, Melissa, Russi, Alvaro H. Serrano, Brick, Lauren, Kozenko, Mariya, Earl, Dawn L., Tham, Emma, Nishimura, Gen, Phillips, John A., Gahl, William A., Hamid, Rizwan, Jackson, Andrew P., Grigelioniene, Giedre, Bober, Michael B.
Publicado 2020

A library of induced pluripotent stem cells from clinically well-characterized, diverse healthy human individuals

por Schaniel, Christoph, Dhanan, Priyanka, Hu, Bin, Xiong, Yuguang, Raghunandan, Teeya, Gonzalez, David M., Dariolli, Rafael, D'Souza, Sunita L., Yadaw, Arjun S., Hansen, Jens, Jayaraman, Gomathi, Mathew, Bino, Machado, Moara, Berger, Seth I., Tripodi, Joseph, Najfeld, Vesna, Garg, Jalaj, Miller, Marc, Surlyn, Colleen S., Michelis, Katherine C., Tangirala, Neelima C., Weerahandi, Himali, Thomas, David C., Beaumont, Kristin G., Sebra, Robert, Mahajan, Milind, Schadt, Eric, Vidovic, Dusica, Schürer, Stephan C., Goldfarb, Joseph, Azeloglu, Evren U., Birtwistle, Marc R., Sobie, Eric A., Kovacic, Jason C., Dubois, Nicole C., Iyengar, Ravi
Publicado 2021

The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders

por Saffari, Afshin, Lau, Tracy, Tajsharghi, Homa, Karimiani, Ehsan Ghayoor, Kariminejad, Ariana, Efthymiou, Stephanie, Zifarelli, Giovanni, Sultan, Tipu, Toosi, Mehran Beiraghi, Sedighzadeh, Sahar, Siu, Victoria Mok, Ortigoza-Escobar, Juan Darío, AlShamsi, Aisha M, Ibrahim, Shahnaz, Al-Sannaa, Nouriya Abbas, Al-Hertani, Walla, Sandra, Whalen, Tarnopolsky, Mark, Alavi, Shahryar, Li, Chumei, Day-Salvatore, Debra-Lynn, Martínez-González, Maria Jesús, Levandoski, Kristin M, Bedoukian, Emma, Madan-Khetarpal, Suneeta, Idleburg, Michaela J, Menezes, Minal Juliet, Siddharth, Aishwarya, Platzer, Konrad, Oppermann, Henry, Smitka, Martin, Collins, Felicity, Lek, Monkol, Shahrooei, Mohmmad, Ghavideldarestani, Maryam, Herman, Isabella, Rendu, John, Faure, Julien, Baker, Janice, Bhambhani, Vikas, Calderwood, Laurel, Akhondian, Javad, Imannezhad, Shima, Mirzadeh, Hanieh Sadat, Hashemi, Narges, Doosti, Mohammad, Safi, Mojtaba, Ahangari, Najmeh, Torbati, Paria Najarzadeh, Abedini, Soheila, Salpietro, Vincenzo, Gulec, Elif Yilmaz, Eshaghian, Safieh, Ghazavi, Mohammadreza, Pascher, Michael T, Vogel, Marina, Abicht, Angela, Moutton, Sébastien, Bruel, Ange-Line, Rieubland, Claudine, Gallati, Sabina, Strom, Tim M, Lochmüller, Hanns, Mohammadi, Mohammad Hasan, Alvi, Javeria Raza, Zackai, Elaine H, Keena, Beth A, Skraban, Cara M, Berger, Seth I, Andrew, Erin H, Rahimian, Elham, Morrow, Michelle M, Wentzensen, Ingrid M, Millan, Francisca, Henderson, Lindsay B, Dafsari, Hormos Salimi, Jungbluth, Heinz, Gomez-Ospina, Natalia, McRae, Anne, Peter, Merlene, Veltra, Danai, Marinakis, Nikolaos M, Sofocleous, Christalena, Ashrafzadeh, Farah, Pehlivan, Davut, Lemke, Johannes R, Melki, Judith, Benezit, Audrey, Bauer, Peter, Weis, Denisa, Lupski, James R, Senderek, Jan, Christodoulou, John, Chung, Wendy K, Goodchild, Rose, Offiah, Amaka C, Moreno-De-Luca, Andres, Suri, Mohnish, Ebrahimi-Fakhari, Darius, Houlden, Henry, Maroofian, Reza
Publicado 2023