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
1986 1
1987 1
1988 1
1989 1
1991 1
1992 2
1993 5
1994 3
1995 2
1996 4
1997 2
1998 3
1999 5
2000 8
2001 7
2002 3
2003 5
2004 3
2005 5
2006 3
2007 4
2008 6
2009 5
2010 5
2011 2
2012 3
2013 8
2014 3
2015 6
2016 8
2017 7
2018 6
2019 1
2020 7
2021 10
2022 5
2023 4
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

144 results

Results by year

Filters applied: . Clear all
Page 1
IL-15, gluten and HLA-DQ8 drive tissue destruction in coeliac disease.
Abadie V, Kim SM, Lejeune T, Palanski BA, Ernest JD, Tastet O, Voisine J, Discepolo V, Marietta EV, Hawash MBF, Ciszewski C, Bouziat R, Panigrahi K, Horwath I, Zurenski MA, Lawrence I, Dumaine A, Yotova V, Grenier JC, Murray JA, Khosla C, Barreiro LB, Jabri B. Abadie V, et al. Nature. 2020 Feb;578(7796):600-604. doi: 10.1038/s41586-020-2003-8. Epub 2020 Feb 12. Nature. 2020. PMID: 32051586 Free PMC article.
Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism.
Chopra M, McEntagart M, Clayton-Smith J, Platzer K, Shukla A, Girisha KM, Kaur A, Kaur P, Pfundt R, Veenstra-Knol H, Mancini GMS, Cappuccio G, Brunetti-Pierri N, Kortüm F, Hempel M, Denecke J, Lehman A; CAUSES Study; Kleefstra T, Stuurman KE, Wilke M, Thompson ML, Bebin EM, Bijlsma EK, Hoffer MJV, Peeters-Scholte C, Slavotinek A, Weiss WA, Yip T, Hodoglugil U, Whittle A, diMonda J, Neira J, Yang S, Kirby A, Pinz H, Lechner R, Sleutels F, Helbig I, McKeown S, Helbig K, Willaert R, Juusola J, Semotok J, Hadonou M, Short J; Genomics England Research Consortium; Yachelevich N, Lala S, Fernández-Jaen A, Pelayo JP, Klöckner C, Kamphausen SB, Abou Jamra R, Arelin M, Innes AM, Niskakoski A, Amin S, Williams M, Evans J, Smithson S, Smedley D, de Burca A, Kini U, Delatycki MB, Gallacher L, Yeung A, Pais L, Field M, Martin E, Charles P, Courtin T, Keren B, Iascone M, Cereda A, Poke G, Abadie V, Chalouhi C, Parthasarathy P, Halliday BJ, Robertson SP, Lyonnet S, Amiel J, Gordon CT. Chopra M, et al. Among authors: abadie v. Am J Hum Genet. 2021 Jun 3;108(6):1138-1150. doi: 10.1016/j.ajhg.2021.04.007. Epub 2021 Apr 27. Am J Hum Genet. 2021. PMID: 33909992 Free PMC article.
Restoring tolerance with antigen delivery.
Jabri B, Abadie V. Jabri B, et al. Among authors: abadie v. Science. 2024 Jan 5;383(6678):30-32. doi: 10.1126/science.adg7505. Epub 2024 Jan 4. Science. 2024. PMID: 38175899
A Mouse Model of Celiac Disease.
Abadie V, Khosla C, Jabri B. Abadie V, et al. Curr Protoc. 2022 Aug;2(8):e515. doi: 10.1002/cpz1.515. Curr Protoc. 2022. PMID: 35994521 Free PMC article.
[Fetal oral immobility syndrome].
Couly G, Aubry MC, Abadie V. Couly G, et al. Among authors: abadie v. Arch Pediatr. 2010 Jan;17(1):1-2. doi: 10.1016/j.arcped.2009.10.011. Epub 2009 Nov 26. Arch Pediatr. 2010. PMID: 19944574 French. No abstract available.
Managing infants with craniofacial malformations - Where to go next?
Poets CF, Abadie V, Breugem C, Wallis C, Abel F, Chalouhi C, Kruisinga F, Sorg AL, Wiechers C. Poets CF, et al. Among authors: abadie v. Semin Fetal Neonatal Med. 2021 Dec;26(6):101289. doi: 10.1016/j.siny.2021.101289. Epub 2021 Sep 17. Semin Fetal Neonatal Med. 2021. PMID: 34548245 Review.
Retrospective evaluation of clinical and molecular data of 148 cases of esophageal atresia.
Ranza E, Le Gouez M, Guimier A, Dunlop NK, Beaudoin S, Malan V, Michot C, Baujat G, Rio M, Cormier-Daire V, Abadie V, Sarnacki S, Delacourt C, Lyonnet S, Attié-Bitach T, Pingault V, Rousseau V, Amiel J. Ranza E, et al. Among authors: abadie v. Am J Med Genet A. 2023 Jan;191(1):77-83. doi: 10.1002/ajmg.a.62989. Epub 2022 Oct 21. Am J Med Genet A. 2023. PMID: 36271508
Congenital feeding and swallowing disorders.
Abadie V, Couly G. Abadie V, et al. Handb Clin Neurol. 2013;113:1539-49. doi: 10.1016/B978-0-444-59565-2.00024-1. Handb Clin Neurol. 2013. PMID: 23622377 Review.
144 results