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

Year Number of Results
1963 1
1964 1
1965 2
1966 1
1975 2
1979 1
1983 3
1987 1
1990 1
2010 1
2013 1
2014 1
2015 6
2016 4
2017 6
2018 5
2019 5
2020 4
2021 4
2022 3
2023 2
2024 3

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53 results

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Page 1
Nano-CUT&Tag for multimodal chromatin profiling at single-cell resolution.
Bárcenas-Walls JR, Ansaloni F, Hervé B, Strandback E, Nyman T, Castelo-Branco G, Bartošovič M. Bárcenas-Walls JR, et al. Among authors: herve b. Nat Protoc. 2024 Mar;19(3):791-830. doi: 10.1038/s41596-023-00932-6. Epub 2023 Dec 21. Nat Protoc. 2024. PMID: 38129675 Review.
2p25.3 microduplications involving MYT1L: further phenotypic characterization through an assessment of 16 new cases and a literature review.
Bouassida M, Egloff M, Levy J, Chatron N, Bernardini L, Le Guyader G, Tabet AC, Schluth-Bolard C, Brancati F, Giuffrida MG, Dard R, Clorennec J, Coursimault J, Vialard F, Hervé B. Bouassida M, et al. Among authors: herve b. Eur J Hum Genet. 2023 Aug;31(8):895-904. doi: 10.1038/s41431-023-01379-9. Epub 2023 May 15. Eur J Hum Genet. 2023. PMID: 37188826 Review.
Prenatal findings in 1p36 deletion syndrome: New cases and a literature review.
Guterman S, Beneteau C, Redon S, Dupont C, Missirian C, Jaeger P, Herve B, Jacquin C, Douet-Guilbert N, Till M, Tabet AC, Moradkhani K, Malan V, Doco-Fenzy M, Vialard F. Guterman S, et al. Among authors: herve b. Prenat Diagn. 2019 Sep;39(10):871-882. doi: 10.1002/pd.5498. Epub 2019 Jul 5. Prenat Diagn. 2019. PMID: 31172545 Review.
[Early recurrent miscarriage: Evaluation and management].
Gallot V, Nedellec S, Capmas P, Legendre G, Lejeune-Saada V, Subtil D, Nizard J, Levêque J, Deffieux X, Hervé B, Vialard F. Gallot V, et al. Among authors: herve b. J Gynecol Obstet Biol Reprod (Paris). 2014 Dec;43(10):812-41. doi: 10.1016/j.jgyn.2014.09.014. Epub 2014 Nov 6. J Gynecol Obstet Biol Reprod (Paris). 2014. PMID: 25447363 Review. French.
Exome sequencing as a first-tier test for copy number variant detection: retrospective evaluation and prospective screening in 2418 cases.
Testard Q, Vanhoye X, Yauy K, Naud ME, Vieville G, Rousseau F, Dauriat B, Marquet V, Bourthoumieu S, Geneviève D, Gatinois V, Wells C, Willems M, Coubes C, Pinson L, Dard R, Tessier A, Hervé B, Vialard F, Harzallah I, Touraine R, Cogné B, Deb W, Besnard T, Pichon O, Laudier B, Mesnard L, Doreille A, Busa T, Missirian C, Satre V, Coutton C, Celse T, Harbuz R, Raymond L, Taly JF, Thevenon J. Testard Q, et al. Among authors: herve b. J Med Genet. 2022 Dec;59(12):1234-1240. doi: 10.1136/jmg-2022-108439. Epub 2022 Sep 22. J Med Genet. 2022. PMID: 36137615
DNA ligase IV deficiency: Immunoglobulin class deficiency depends on the genotype.
Dard R, Herve B, Leblanc T, de Villartay JP, Collopy L, Vulliami T, Drunat S, Gorde S, Babik A, Souchon PF, Agadr A, Abilkassem R, Elalloussi M, Verloes A, Doco-Fenzy M. Dard R, et al. Among authors: herve b. Pediatr Allergy Immunol. 2017 May;28(3):298-303. doi: 10.1111/pai.12694. Epub 2017 Feb 22. Pediatr Allergy Immunol. 2017. PMID: 28039949 Review. No abstract available.
IgH 3' regulatory region increases ectopic class switch recombination.
Le Noir S, Bonaud A, Hervé B, Baylet A, Boyer F, Lecardeur S, Oruc Z, Sirac C, Cogné M. Le Noir S, et al. Among authors: herve b. PLoS Genet. 2021 Feb 8;17(2):e1009288. doi: 10.1371/journal.pgen.1009288. eCollection 2021 Feb. PLoS Genet. 2021. PMID: 33556079 Free PMC article.
Immunoglobulin light-chain toxicity in a mouse model of monoclonal immunoglobulin light-chain deposition disease.
Bender S, Ayala MV, Bonaud A, Javaugue V, Carrion C, Oblet C, Rinsant A, Kaaki S, Oruc Z, Boyer F, Paquet A, Pons N, Hervé B, Ashi MO, Jaccard A, Delpy L, Touchard G, Cogné M, Bridoux F, Sirac C. Bender S, et al. Among authors: herve b. Blood. 2020 Oct 1;136(14):1645-1656. doi: 10.1182/blood.2020005980. Blood. 2020. PMID: 32559766 Free article.
53 results