K. Mondal

发表

Design and isolation of temperature-sensitive mutants of Gal4 in yeast and Drosophila.

Raghavan Varadarajan, Guramrit Singh, R. Varadarajan, 2007, Journal of molecular biology.

Design and Utility of Temperature-Sensitive Gal4 Mutants for Conditional Gene Expression in Drosophila

Raghavan Varadarajan, R. Varadarajan, K. VijayRaghavan, 2007, Fly.

Design of temperature-sensitive mutants solely from amino acid sequence.

Raghavan Varadarajan, Guramrit Singh, R. Varadarajan, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Microarray oligonucleotide probe designer (MOPeD): A web service.

Vanessa L. Horner, D. Cutler, M. Zwick, 2010, Open access bioinformatics.

Excess variants in AFF 2 detected by massively parallel sequencing of males with autism spectrum disorder

D. Cutler, M. Zwick, V. Patel, 2012 .

Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients With Crohn's Disease.

David T. Okou, M. Daly, R. Xavier, 2018, Gastroenterology.

Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse

Vanessa L. Horner, D. Cutler, M. Zwick, 2012, G3: Genes | Genomes | Genetics.

Microarray oligonucleotide probe designer: a Web service

Vanessa L. Horner, D. Cutler, M. Zwick, 2010 .

Exome Sequencing Identifies a Novel FOXP3 Mutation in a 2-Generation Family With Inflammatory Bowel Disease

David T. Okou, D. Cutler, S. Kugathasan, 2014, Journal of pediatric gastroenterology and nutrition.

Rational elicitation of cold-sensitive phenotypes

R. Varadarajan, K. VijayRaghavan, A. Bhattacharjee, 2016, Proceedings of the National Academy of Sciences.

The Effect of Early‐Life Environmental Exposures on Disease Phenotype and Clinical Course of Crohn's Disease in Children

Ajay S. Gulati, A. Griffiths, R. Baldassano, 2018, The American Journal of Gastroenterology.

SeqAnt 2012: Recent Developments in Next-Generation Sequencing Annotation

Matthew Ezewudo, Promita Bose, Michael E. Zwick, 2012 .

Dissecting Allele Architecture of Early Onset IBD Using High-Density Genotyping

David T. Okou, D. Cutler, A. Griffiths, 2015, PloS one.

Prediction of complicated disease course for children newly diagnosed with Crohn's disease: a multicentre inception cohort study

Judy H. Cho, C. Huttenhower, R. Xavier, 2017, The Lancet.

Association Between Plasma Level of Collagen Type III Alpha 1 Chain and Development of Strictures in Pediatric Patients With Crohn's Disease.

R. Baldassano, M. Dubinsky, N. LeLeiko, 2019, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Excess variants in AFF2 detected by massively parallel sequencing of males with autism spectrum disorder.

Michael E Zwick, Promita Bose, David J Cutler, 2012, Human molecular genetics.

Blood-Derived DNA Methylation Signatures of Crohn's Disease and Severity of Intestinal Inflammation.

Judy H. Cho, David T. Okou, D. Cutler, 2019, Gastroenterology.

Targeted sequencing of the human X chromosome exome.

D. Cutler, M. Zwick, A. Shetty, 2011, Genomics.

SeqAnt: A web service to rapidly identify and annotate DNA sequence variations

David J. Cutler, Michael E. Zwick, Amol Carl Shetty, 2010, BMC Bioinformatics.

Evolution of Pediatric Inflammatory Bowel Disease Unclassified (IBD-U): Incorporated With Serological and Gene Expression Profiles.

A. Griffiths, M. Dubinsky, N. LeLeiko, 2018, Inflammatory bowel diseases.

Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder

Donna M. Martin, Jun Z. Li, C. Skinner, 2012, Journal of Medical Genetics.

Transcriptional Risk Scores link GWAS to eQTL and Predict Complications in Crohn's Disease

Judy H. Cho, A. Griffiths, G. Gibson, 2017, Nature Genetics.

Variant ATRX Syndrome with Dysfunction of ATRX and MAGT1 Genes

M. Zwick, F. Wolf, M. O’Driscoll, 2014, Human mutation.

Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte-Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's Disease.

M. Daly, R. Xavier, D. Cutler, 2018, Inflammatory bowel diseases.

NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease

J. Danesh, M. Parkes, J. Kelsen, 2017, Mucosal Immunology.

NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease

Jimmy D Bell, J. Danesh, G. McVean, 2017, Mucosal Immunology.

Variation in Care in the Management of Children With Crohn's Disease: Data From a Multicenter Inception Cohort Study.

A. Griffiths, R. Baldassano, M. Dubinsky, 2019, Inflammatory bowel diseases.

IBD: Genetic differences in Crohn's disease susceptibility and outcome

S. Kugathasan, K. Mondal, 2017, Nature Reviews Gastroenterology &Hepatology.