Network analyses in systems pharmacology

Por Berger, Seth I., Iyengar, Ravi
Publicado em 2009

Role of systems pharmacology in understanding drug adverse events

Por Berger, Seth I., Iyengar, Ravi
Publicado em 2010

Systems pharmacology and genome medicine: a future perspective

Por Wist, Aislyn D, Berger, Seth I, Iyengar, Ravi
Publicado em 2009

AVIS: AJAX viewer of interactive signaling networks

Por Berger, Seth I., Iyengar, Ravi, Ma’ayan, Avi
Publicado em 2007

Systems Pharmacology of Arrhythmias

Por Berger, Seth I., Ma’ayan, Avi, Iyengar, Ravi
Publicado em 2010

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

Por Berger, Seth I, Posner, Jeremy M, Ma'ayan, Avi
Publicado em 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 em 2008

ChEA: transcription factor regulation inferred from integrating genome-wide ChIP-X experiments

Por Lachmann, Alexander, Xu, Huilei, Krishnan, Jayanth, Berger, Seth I., Mazloom, Amin R., Ma'ayan, Avi
Publicado em 2010

Vamping: Stereology-based automated quantification of fluorescent puncta size and density

Por Dumitriu, Dani, Berger, Seth I., Hamo, Carine, Hara, Yuko, Bailey, Megan, Hamo, Amarelle, Grossman, Yael S., Janssen, William G., Morrison, John H.
Publicado em 2012

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 em 2009

SIX3 Deletions and Incomplete Penetrance in Families Affected by Holoprosencephaly

Por Stokes, Bethany, Berger, Seth I., Hall, Beth A., Weiss, Karin, Hadley, Donald W., Murdock, David R., Ramanathan, Subhadra, Clark, Robin D., Roessler, Erich, Kruszka, Paul, Muenke, Maximilian
Publicado no Congenit Anom (Kyoto) (2017)

Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotype

Por Chen, Li, Jensik, Philip J., Alaimo, Joseph T., Walkiewicz, Magdalena, Berger, Seth, Roeder, Elizabeth, Faqeih, Eissa A., Bernstein, Jonathan A., Smith, Ann C. M., Mullegama, Sureni V., Saffen, David W., Elsea, Sarah H.
Publicado no Hum Mutat (2017)

Exome analysis of Smith–Magenis-like syndrome cohort identifies de novo likely pathogenic variants

Por Berger, Seth I., Ciccone, Carla, Simon, Karen L., Malicdan, May Christine, Vilboux, Thierry, Billington, Charles, Fischer, Roxanne, Introne, Wendy J., Gropman, Andrea, Blancato, Jan K., Mullikin, James C., Gahl, William A., Huizing, Marjan, Smith, Ann C. M.
Publicado no Hum Genet (2017)