Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2011 1
2013 1
2014 2
2016 1
2017 2
2018 2
2019 2
2020 4
2021 2
2022 3
2023 4
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

23 results

Results by year

Filters applied: . Clear all
Page 1
Impact of exome sequencing in inflammatory bowel disease.
Cardinale CJ, Kelsen JR, Baldassano RN, Hakonarson H. Cardinale CJ, et al. World J Gastroenterol. 2013 Oct 28;19(40):6721-9. doi: 10.3748/wjg.v19.i40.6721. World J Gastroenterol. 2013. PMID: 24187447 Free PMC article. Review.
Approaches to understanding the genetic contribution to inflammatory bowel disease (IBD) have continuously evolved from family- and population-based epidemiology, to linkage analysis, and most recently, to genome-wide association studies (GWAS). ...In this re …
Approaches to understanding the genetic contribution to inflammatory bowel disease (IBD) have continuously evolved from …
Genomic diagnosis and care co-ordination for monogenic inflammatory bowel disease in children and adults: consensus guideline on behalf of the British Society of Gastroenterology and British Society of Paediatric Gastroenterology, Hepatology and Nutrition.
Kammermeier J, Lamb CA, Jones KDJ, Anderson CA, Baple EL, Bolton C, Braggins H, Coulter TI, Gilmour KC, Gregory V, Hambleton S, Hartley D, Hawthorne AB, Hearn S, Laurence A, Parkes M, Russell RK, Speight RA, Travis S, Wilson DC, Uhlig HH. Kammermeier J, et al. Lancet Gastroenterol Hepatol. 2023 Mar;8(3):271-286. doi: 10.1016/S2468-1253(22)00337-5. Epub 2023 Jan 9. Lancet Gastroenterol Hepatol. 2023. PMID: 36634696 Review.
Genomic medicine enables the identification of patients with rare or ultra-rare monogenic forms of inflammatory bowel disease (IBD) and supports clinical decision making. Patients with monogenic IBD frequently experience extremely early onset of treatment-ref …
Genomic medicine enables the identification of patients with rare or ultra-rare monogenic forms of inflammatory bowel disea
Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients.
Wu Y, Gettler K, Kars ME, Giri M, Li D, Bayrak CS, Zhang P, Jain A, Maffucci P, Sabic K, Van Vleck T, Nadkarni G, Denson LA, Ostrer H, Levine AP, Schiff ER, Segal AW, Kugathasan S, Stenson PD, Cooper DN, Philip Schumm L, Snapper S, Daly MJ, Haritunians T, Duerr RH, Silverberg MS, Rioux JD, Brant SR, McGovern DPB, Cho JH, Itan Y. Wu Y, et al. Nat Commun. 2023 Apr 20;14(1):2256. doi: 10.1038/s41467-023-37849-3. Nat Commun. 2023. PMID: 37080976 Free PMC article.
Inflammatory bowel disease (IBD) is a group of chronic digestive tract inflammatory conditions whose genetic etiology is still poorly understood. ...Finally, we show that polygenic risk score analyses based on genome-wide high impact variants ha
Inflammatory bowel disease (IBD) is a group of chronic digestive tract inflammatory conditions whose genetic eti
Genomic and Immunologic Drivers of Very Early-Onset Inflammatory Bowel Disease.
Conrad MA, Kelsen JR. Conrad MA, et al. Pediatr Dev Pathol. 2019 May-Jun;22(3):183-193. doi: 10.1177/1093526619834807. Epub 2019 Mar 6. Pediatr Dev Pathol. 2019. PMID: 30841788 Free PMC article. Review.
PURPOSE OF REVIEW: Inflammatory bowel disease (IBD) is a multifactorial disease caused by dysregulated immune responses to commensal or pathogenic intestinal microbes, resulting in chronic intestinal inflammation. ...We aim to review the clinical prese …
PURPOSE OF REVIEW: Inflammatory bowel disease (IBD) is a multifactorial disease caused by dysregulated immune re …
The role of monogenic disease in children with very early onset inflammatory bowel disease.
Kelsen JR, Baldassano RN. Kelsen JR, et al. Curr Opin Pediatr. 2017 Oct;29(5):566-571. doi: 10.1097/MOP.0000000000000531. Curr Opin Pediatr. 2017. PMID: 28700415 Free PMC article. Review.
PURPOSE OF REVIEW: Inflammatory bowel disease (IBD) is a multifactorial disease caused by dysregulated immune responses to commensal or pathogenic intestinal microbes, resulting in chronic intestinal inflammation. ...This article will review the advanc …
PURPOSE OF REVIEW: Inflammatory bowel disease (IBD) is a multifactorial disease caused by dysregulated immune re …
Utilization of Whole Exome Sequencing Data to Identify Clinically Relevant Pharmacogenomic Variants in Pediatric Inflammatory Bowel Disease.
Mulder DJ, Khalouei S, Warner N, Gonzaga-Jauregui C, Church PC, Walters TD, Ramani AK, Griffiths AM, Cohn I, Muise AM. Mulder DJ, et al. Clin Transl Gastroenterol. 2020 Dec;11(12):e00263. doi: 10.14309/ctg.0000000000000263. Clin Transl Gastroenterol. 2020. PMID: 33512800 Free PMC article.
INTRODUCTION: We hypothesized that variants within clinically relevant pharmacogenes could be identified using a whole exome sequencing data set derived from a cohort of more than 1,000 patients with inflammatory bowel disease (IBD). METHODS: Pe …
INTRODUCTION: We hypothesized that variants within clinically relevant pharmacogenes could be identified using a whole exome seque
Role of telomere shortening in anticipation of inflammatory bowel disease.
Truta B, Wohler E, Sobreira N, Datta LW, Brant SR. Truta B, et al. World J Gastrointest Pharmacol Ther. 2020 Sep 8;11(4):69-78. doi: 10.4292/wjgpt.v11.i4.69. World J Gastrointest Pharmacol Ther. 2020. PMID: 32953227 Free PMC article.
BACKGROUND: The existence of genetic anticipation has been long disputed in inflammatory bowel disease (IBD) in the absence of the explanatory mechanism. ...We determined telomere length (TL) in lymphocytes and granulocytes from peripheral blood of the affect …
BACKGROUND: The existence of genetic anticipation has been long disputed in inflammatory bowel disease (IBD) in the abs …
Whole exome sequencing analyses reveal gene-microbiota interactions in the context of IBD.
Hu S, Vich Vila A, Gacesa R, Collij V, Stevens C, Fu JM, Wong I, Talkowski ME, Rivas MA, Imhann F, Bolte L, van Dullemen H, Dijkstra G, Visschedijk MC, Festen EA, Xavier RJ, Fu J, Daly MJ, Wijmenga C, Zhernakova A, Kurilshikov A, Weersma RK. Hu S, et al. Gut. 2021 Feb;70(2):285-296. doi: 10.1136/gutjnl-2019-319706. Epub 2020 Jul 10. Gut. 2021. PMID: 32651235 Free PMC article.
Here, we report on the influence of host genetics on the gut microbiome in IBD. DESIGN: To evaluate the impact of host genetics on the gut microbiota of patients with IBD, we combined whole exome sequencing of the host genome and whole genome shotgun seque
Here, we report on the influence of host genetics on the gut microbiome in IBD. DESIGN: To evaluate the impact of host genetics on th …
Genetic analysis of four consanguineous multiplex families with inflammatory bowel disease.
Ben-Yosef N, Frampton M, Schiff ER, Daher S, Abu Baker F, Safadi R, Israeli E, Segal AW, Levine AP. Ben-Yosef N, et al. Gastroenterol Rep (Oxf). 2021 Jul 13;9(6):521-532. doi: 10.1093/gastro/goab007. eCollection 2021 Dec. Gastroenterol Rep (Oxf). 2021. PMID: 34925849 Free PMC article.
BACKGROUND: Family studies support a genetic predisposition to inflammatory bowel diseases (IBD), but known genetic variants only partially explain the disease heritability. ...In a family-specific analysis, we utilised homozygosity mapping complemente …
BACKGROUND: Family studies support a genetic predisposition to inflammatory bowel diseases (IBD), but known genetic var …
Human genome meeting 2016 : Houston, TX, USA. 28 February - 2 March 2016.
Srivastava AK, Wang Y, Huang R, Skinner C, Thompson T, Pollard L, Wood T, Luo F, Stevenson R, Polimanti R, Gelernter J, Lin X, Lim IY, Wu Y, Teh AL, Chen L, Aris IM, Soh SE, Tint MT, MacIsaac JL, Yap F, Kwek K, Saw SM, Kobor MS, Meaney MJ, Godfrey KM, Chong YS, Holbrook JD, Lee YS, Gluckman PD, Karnani N; GUSTO study group; Kapoor A, Lee D, Chakravarti A, Maercker C, Graf F, Boutros M, Stamoulis G, Santoni F, Makrythanasis P, Letourneau A, Guipponi M, Panousis N, Garieri M, Ribaux P, Falconnet E, Borel C, Antonarakis SE, Kumar S, Curran J, Blangero J, Chatterjee S, Kapoor A, Akiyama J, Auer D, Berrios C, Pennacchio L, Chakravarti A, Donti TR, Cappuccio G, Miller M, Atwal P, Kennedy A, Cardon A, Bacino C, Emrick L, Hertecant J, Baumer F, Porter B, Bainbridge M, Bonnen P, Graham B, Sutton R, Sun Q, Elsea S, Hu Z, Wang P, Zhu Y, Zhao J, Xiong M, Bennett DA, Hidalgo-Miranda A, Romero-Cordoba S, Rodriguez-Cuevas S, Rebollar-Vega R, Tagliabue E, Iorio M, D’Ippolito E, Baroni S, Kaczkowski B, Tanaka Y, Kawaji H, Sandelin A, Andersson R, Itoh M, Lassmann T; The FANTOM5 Consortium; Hayashizaki Y, Carninci P, Forrest ARR, Semple CA, Rosenthal EA, Shirts B, Amendola L, Gallego C, Horike-Pyne… See abstract for full author list ➔ Srivastava AK, et al. Hum Genomics. 2016 May 26;10 Suppl 1(Suppl 1):12. doi: 10.1186/s40246-016-0063-5. Hum Genomics. 2016. PMID: 27294413 Free PMC article.
Shaya, E. Stone O29 PhenoDB and genematcher, solving unsolved whole exome sequencing data N. L. Sobreira, F. Schiettecatte, H. Ling, E. ...Myrzakhmetova P7 Frequency of Xmn1 polymorphism among sickle cell carrier cases in UAE population M. Matar P8 Differentiating …
Shaya, E. Stone O29 PhenoDB and genematcher, solving unsolved whole exome sequencing data N. L. Sobreira, F. Schiettecatte, H. …
23 results