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Christine R. Stevens · SciRah

Researcher profile · Semantic Scholar

Christine R. Stevens

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Christine R. Stevens — researcher profile on SciRah

h-index: 40
Works: 86
Citations: 17K

Most-cited papers

Identification of common genetic risk variants for autism spectrum disorder
J. Grove, S. Ripke, T. Als, M. Mattheisen +272 more
2019Nature Genetics2,146 citations Open access
Semantic Scholar
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Satterstrom, Jack A. Kosmicki, Jiebiao Wang, M. Breen +186 more
2019Cell2,103 citations Open access
Semantic Scholar
Discovery of the first genome-wide significant risk loci for attention-deficit/hyperactivity disorder
D. Demontis, R. Walters, Joanna Martin, M. Mattheisen +217 more
2018Nature Genetics1,852 citations Open access
Semantic Scholar
Patterns and rates of exonic de novo mutations in autism spectrum disorders
B. Neale, Y. Kou, Li Liu, Avi Ma’ayan +55 more
2012Nature1,781 citations Open access
Semantic Scholar
A framework for the interpretation of de novo mutation in human disease
K. Samocha, E. Robinson, Stephan J Sanders, Christine R. Stevens +22 more
2014Nature Genetics1,048 citations Open access
Semantic Scholar
A structural variation reference for medical and population genetics
Ryan L. Collins, H. Brand, K. Karczewski, Xue-Fang Zhao +180 more
2020Nature932 citations Open access
Semantic Scholar
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
M. Rivas, M. Beaudoin, A. Gardet, Christine R. Stevens +34 more
2011Nature Genetics818 citations Open access
Semantic Scholar
Rare coding variants in 10 genes confer substantial risk for schizophrenia
T. Singh, T. Poterba, D. Curtis, H. Akil +107 more
2022Nature687 citations Open access
Semantic Scholar
Defining the Role of the MHC in Autoimmunity: A Review and Pooled Analysis
M. Fernando, Christine R. Stevens, E. Walsh, P. De Jager +4 more
2008PLoS Genetics642 citations Open access
Semantic Scholar
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Jack M. Fu, F. Satterstrom, Minshi Peng, H. Brand +113 more
2022Nature Genetics554 citations Open access
Semantic Scholar
Using whole exome sequencing to identify inherited causes of autism
Timothy W. Yu, Maria H. Chahrour, Michael E. Coulter, S. Jiralerspong +45 more
2013Neuron452 citations Open access
Semantic Scholar
LRRK2 Is Involved in the IFN-γ Response and Host Response to Pathogens
A. Gardet, Yair Benita, Chun Li, B. Sands +7 more
2010Journal of Immunology387 citations Open access
Semantic Scholar
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders
Elaine T. Lim, S. Raychaudhuri, Stephan J Sanders, Christine R. Stevens +36 more
2013Neuron283 citations Open access
Semantic Scholar
Mutations causing medullary cystic kidney disease type 1 (MCKD1) lie in a large VNTR in MUC1 missed by massively parallel sequencing
Andrew W. Kirby, A. Gnirke, D. Jaffe, V. Barešová +39 more
2013Nature Genetics281 citations Open access
Semantic Scholar
zCall: a rare variant caller for array-based genotyping: Genetics and population analysis
J. Goldstein, Andrew Crenshaw, Jason P. Carey, George B. Grant +13 more
2012Bioinform.232 citations Open access
Semantic Scholar
Discovery of the first genome-wide significant risk loci for ADHD
D. Demontis, R. Walters, Joanna Martin, M. Mattheisen +67 more
2017bioRxiv231 citations Open access
Semantic Scholar
Deep Resequencing of GWAS Loci Identifies Rare Variants in CARD9, IL23R and RNF186 That Are Associated with Ulcerative Colitis
M. Beaudoin, P. Goyette, G. Boucher, Ken-Sin Lo +30 more
2013PLoS Genetics214 citations Open access
Semantic Scholar
Whole-Exome Sequencing and Homozygosity Analysis Implicate Depolarization-Regulated Neuronal Genes in Autism
Maria H. Chahrour, Timothy W. Yu, Elaine T. Lim, Bulent Ataman +7 more
2012PLoS Genetics195 citations Open access
Semantic Scholar
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome.
M. Manzini, Dimira E. Tambunan, R. Hill, Timothy W. Yu +18 more
2012American Journal of Human Genetics187 citations Open access
Semantic Scholar
Identification of Two Independent Risk Factors for Lupus within the MHC in United Kingdom Families
M. Fernando, Christine R. Stevens, Pardis C Sabeti, E. Walsh +5 more
2007PLoS Genetics187 citations Open access
Semantic Scholar
Autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD) have a similar burden of rare protein-truncating variants
F. Satterstrom, R. Walters, T. Singh, E. Wigdor +18 more
2019Nature Neuroscience176 citations Open access
Semantic Scholar
Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder.
C. Poultney, A. P. Goldberg, Elodie Drapeau, Y. Kou +11 more
2013American Journal of Human Genetics169 citations Open access
Semantic Scholar
Host genetic variation and its microbiome interactions within the Human Microbiome Project
R. Kolde, E. Franzosa, Gholamali Rahnavard, A. B. Hall +5 more
2018Genome Medicine160 citations Open access
Semantic Scholar
Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility
Aleksejs Sazonovs, Christine R. Stevens, G. Venkataraman, K. Yuan +126 more
2022Nature Genetics159 citations Open access
Semantic Scholar
Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls
Li Liu, A. Sabo, B. Neale, U. Nagaswamy +33 more
2013PLoS Genetics141 citations Open access
Semantic Scholar
Evolution of Osteocrin as an activity-regulated factor in the primate brain
Bulent Ataman, G. Boulting, D. Harmin, Marty G. Yang +20 more
2016Nature139 citations Open access
Semantic Scholar
Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia
T. Singh, T. Poterba, David Curtis, H. Akil +106 more
2020medRxiv111 citations Open access
Semantic Scholar
Common risk variants identified in autism spectrum disorder
J. Grove, S. Ripke, T. Als, M. Mattheisen +71 more
2017bioRxiv105 citations Open access
Semantic Scholar
Cellular and inter-cellular rewiring of the human colon during ulcerative colitis
C. Smillie, M. Biton, J. Ordovas-Montañes, M. Keri +32 more
201986 citations
Semantic Scholar
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population
M. Rivas, B. Avila, J. Koskela, Hai-Liang Huang +53 more
2016bioRxiv83 citations Open access
Semantic Scholar
Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients with Crohn’s Disease
L. Denson, I. Jurickova, R. Karns, K. Shaw +30 more
2018Gastroenterology81 citations Open access
Semantic Scholar
An open resource of structural variation for medical and population genetics
Ryan L. Collins, H. Brand, K. Karczewski, Xue-Fang Zhao +41 more
201976 citations Open access
Semantic Scholar
A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis
M. Rivas, D. Graham, P. Sulem, Christine R. Stevens +86 more
2015Nature Communications66 citations Open access
Semantic Scholar
Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk
F. Satterstrom, Jack A. Kosmicki, Jiebiao Wang, M. Breen +153 more
2018bioRxiv60 citations Open access
Semantic Scholar
Established Genetic Risk Factors Do Not Distinguish Early and Later Onset Crohn’s Disease
J. Essers, Jessica J. Lee, S. Kugathasan, Christine R. Stevens +2 more
2009Inflammatory Bowel Diseases56 citations Open access
Semantic Scholar
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies.
Chelsea Lowther, E. Valkanas, J. Giordano, Harold Wang +41 more
2023American Journal of Human Genetics54 citations Open access
Semantic Scholar
SMAD3 gene variant is a risk factor for recurrent surgery in patients with Crohn’s disease
S. Fowler, A. Ananthakrishnan, A. Gardet, Christine R. Stevens +5 more
2014Journal of Crohn's & Colitis54 citations Open access
Semantic Scholar
Whole exome sequencing analyses reveal gene–microbiota interactions in the context of IBD
Shixian Hu, Arnau Vich Vila, R. Gacesa, V. Collij +18 more
2020Gut50 citations Open access
Semantic Scholar
High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA
J. Poulsen, F. Lescai, J. Grove, M. Bækvad-Hansen +16 more
2016PLoS ONE41 citations Open access
Semantic Scholar
PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features
R. Khalil, Connor J. Kenny, R. Hill, G. Mochida +12 more
2018American Journal of Medical Genetics Part B: Neuropsychiatric Genetics40 citations Open access
Semantic Scholar
Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease
Hari Somineni, Sini Nagpal, S. Venkateswaran, D. Cutler +54 more
2021American Journal of Human Genetics36 citations Open access
Semantic Scholar
Genetic modifiers of hypertension in soluble guanylate cyclase α1-deficient mice.
E. Buys, Michael J. Raher, Andrew W. Kirby, M. Shahid +17 more
2012Journal of Clinical Investigation36 citations Open access
Semantic Scholar
Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism
Jack M. Fu, F. Satterstrom, Minshi Peng, H. Brand +61 more
2021medRxiv34 citations Open access
Semantic Scholar
MAST3: a Novel IBD Risk Factor that Modulates TLR4 Signaling
C. Labbé, P. Goyette, C. Lefebvre, Christine R. Stevens +16 more
2008Genes and Immunity33 citations Open access
Semantic Scholar
ASD and ADHD have a similar burden of rare protein-truncating variants
F. Satterstrom, Raymond K. Walters, T. Singh, E. Wigdor +18 more
2018bioRxiv29 citations Open access
Semantic Scholar
Genetic variants and pathways implicated in a pediatric inflammatory bowel disease cohort
K. Shaw, D. Cutler, David T. Okou, Anne F. Dodd +20 more
2018Genes and Immunity29 citations Open access
Semantic Scholar
Genetic risk for schizophrenia and autism, social impairment and developmental pathways to psychosis
E. Velthorst, S. Froudist-Walsh, E. Stahl, D. Ruderfer +51 more
2018Translational Psychiatry25 citations Open access
Semantic Scholar
Rare coding variants in 10 genes confer substantial risk for schizophrenia
T. Singh, T. Poterba, David Curtis, Huda Akil +118 more
202323 citations
Semantic Scholar
Prevalence and Effect of Genetic Risk of Thrombo-embolic Disease in Inflammatory Bowel Disease
Takeo Naito, Gregory J. Botwin, T. Haritunians, Dalin Li +9 more
2020Gastroenterology19 citations Open access
Semantic Scholar
Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte-Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's Disease.
L. Denson, I. Jurickova, R. Karns, K. Shaw +30 more
2018Inflammatory Bowel Diseases16 citations Open access
Semantic Scholar

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