Nicolas Thierry-Mieg's publications

Back to my home page.

This should list all my published papers (but check the "last modified" date at the bottom).
I've compiled a more detailed list, including talks and posters, for my work related to smart-pooling.

In addition you can look for my papers on pubmed, google scholar, HAL, orcid, or maybe DBLP (for computer science stuff).

57. Amiri-Yekta A, Sen S, Hazane-Puch F, Tebbakh C, Roux-Buisson N, Cazin C, Thierry-Mieg N, Bouras A, Mohammad Ali SG, Hosseini SH, Goodarzian M, Gourabi H, Ray PF, Kherraf ZE.
Whole genome sequencing identifies a homozygous splicing variant in TDRKH segregating with non-obstructive azoospermia in an Iranian family.
Clin Genet. 2024 Jul 2. doi: 10.1111/cge.14584. Epub ahead of print. pdf. Full text online.

56. Muroňová J, Kherraf ZE, Giordani E, Lambert E, Eckert S, Cazin C, Amiri-Yekta A, Court M, Chevalier G, Martinez G, Neirijnck Y, Kühne F, Wehrli L, Klena N, Hamel V, De Macedo L, Escoffier J, Guichard P, Coutton C, Mustapha SFB, Kharouf M, Bouin AP, Zouari R, Thierry-Mieg N, Nef S, Geimer S, Loeuillet C, Ray PF, Arnoult C.
Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse.
Elife. 2024 Mar 5;12:RP86845. doi: 10.7554/eLife.86845. pdf. Full text online.

55. Jreijiri F, Cavarocchi E, Amiri-Yekta A, Cazin C, Hosseini SH, El Khouri E, Patrat C, Thierry-Mieg N, Ray PF, Dulioust E, Whitfield M, Touré A.
CCDC65, encoding a component of the axonemal Nexin-Dynein regulatory complex, is required for sperm flagellum structure in humans.
Clin Genet. 2024 Mar;105(3):317-322. doi: 10.1111/cge.14459. Epub 2023 Nov 17. Full text online.

54. Kherraf ZE, Barbotin AL, Martinez G, Mazet A, Cazin C, Coutton C, Arnoult C, Thierry-Mieg N, Rives N, Rives-Feraille A, Ray PF.
A splice donor variant of GAS8 induces structural disorganization of the axoneme in sperm flagella and leads to nonsyndromic male infertility.
Clin Genet. 2024 Feb;105(2):220-225. doi:10.1111/cge.14450. Epub 2023 Nov 11. pdf. Full text online.

53. Dacheux D, Martinez G, Broster Reix CE, Beurois J, Lores P, Tounkara M, Dupuy JW, Robinson DR, Loeuillet C, Lambert E, Wehbe Z, Escoffier J, Amiri-Yekta A, Daneshipour A, Hosseini SH, Zouari R, Mustapha SFB, Halouani L, Jiang X, Shen Y, Liu C, Thierry-Mieg N, Septier A, Bidart M, Satre V, Cazin C, Kherraf ZE, Arnoult C, Ray PF, Toure A, Bonhivers M, Coutton C.
Novel axonemal protein ZMYND12 interacts with TTC29 and DNAH1, and is required for male fertility and flagellum function.
Elife. 2023 Nov 7;12:RP87698. doi: 10.7554/eLife.87698. pdf. Full text online.

52. Cavarocchi E, Sayou C, Lorès P, Cazin C, Stouvenel L, El Khouri E, Coutton C, Kherraf ZE, Patrat C, Govin J, Thierry-Mieg N, Whitfield M, Ray PF, Dulioust E, Touré A.
Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans.
iScience. 2023 Jul 10;26(8):107354. doi: 10.1016/j.isci.2023.107354. pdf. Full text online.

51. Coudert A, Cazin C, Amiri-Yekta A, Ben Mustapha SF, Zouari R, Bessonat J, Zoghmar A, Clergeau A, Metzler-Guillemain C, Triki C, Lejeune H, Sermondade N, Pipiras E, Prisant N, Cedrin I, Koscinski I, Keskes L, Lestrade F, Hesters L, Rives N, Dorphin B, Guichet A, Patrat C, Dulioust E, Feraille A, Robert F, Brouillet S, Morel F, Perrin A, Rougier N, Bieth E, Sorlin A, Siffroi JP, Ben Khelifa M, Boiterelle F, Hennebicq S, Satre V, Arnoult C, Coutton C, Barbotin AL, Thierry-Mieg N, Kherraf ZE, Ray PF.
Genetic causes of macrozoospermia and proposal for an optimized genetic diagnosis strategy based on sperm parameters.
J Genet Genomics. 2023 Jul;50(7):536-540. doi: 10.1016/j.jgg.2023.04.007. Epub 2023 Apr 26. pdf.

50. Martinez G, Barbotin AL, Cazin C, Wehbe Z, Boursier A, Amiri-Yekta A, Daneshipour A, Hosseini SH, Rives N, Feraille A, Thierry-Mieg N, Bidart M, Satre V, Arnoult C, Ray PF, Kherraf ZE, Coutton C.
New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella.
Int J Mol Sci. 2023 Jan 29;24(3):2559. doi: 10.3390/ijms24032559. pdf. Full text online.

49. Saini PK, Dawitz H, Aufschnaiter A, Bondarev S, Thomas J, Amblard A, Stewart J, Thierry-Mieg N, Ott M, Pierrel F.
The [PSI+] prion modulates cytochrome c oxidase deficiency caused by deletion of COX12.
Mol Biol Cell. 2022 Dec 1;33(14):ar130. doi: 10.1091/mbc.E21-10-0499. pdf. Full text online.

48. Loeuillet C, Dhellemmes M, Cazin C, Kherraf ZE, Fourati Ben Mustapha S, Zouari R, Thierry-Mieg N, Arnoult C, Ray PF.
A recurrent ZP1 variant is responsible for Oocyte Maturation Defect with degenerated oocytes in infertile females.
Clin Genet. 2022 Jul;102(1):22-29. doi: 10.1111/cge.14144. Epub 2022 Jun 1. pdf. Full text online.

47. Kherraf ZE, Cazin C, Lestrade F, Muronova J, Coutton C, Arnoult C, Thierry-Mieg N, Ray PF.
From azoospermia to macrozoospermia, a phenotypic continuum due to mutations in the ZMYND15 gene.
Asian J Androl. 2022 May-Jun;24(3):243-247. doi: 10.4103/aja202194. pdf. Full text online.

46. Kherraf ZE, Cazin C, Bouker A, Fourati Ben Mustapha S, Hennebicq S, Septier A, Coutton C, Raymond L, Nouchy M, Thierry-Mieg N, Zouari R, Arnoult C, Ray PF.
Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermia.
Am J Hum Genet. 2022 Mar 3;109(3):508-517. doi: 10.1016/j.ajhg.2022.01.011. Epub 2022 Feb 15. pdf. Full text online.

45. Cazin C, Neirijnck Y, Loeuillet C, Wehrli L, Kühne F, Lordey I, Mustapha SFB, Bouker A, Zouari R, Thierry-Mieg N, Nef S, Arnoult C, Ray PF, Kherraf ZE.
Combined Use of Whole Exome Sequencing and CRISPR/Cas9 to Study the Etiology of Non-Obstructive Azoospermia: Demonstration of the Dispensable Role of the Testis-Specific Genes C1orf185 and CCT6B.
Cells 2022, 11(1):118. doi: 10.3390/cells11010118. pdf. Full text online.

44. Shen Q, Martinez G, Liu H, Beurois J, Wu H, Amiri-Yekta A, Liang D, Kherraf ZE, Bidart M, Cazin C, Celse T, Satre V, Thierry-Mieg N, Whitfield M, Touré A, Song B, Lv M, Li K, Liu C, Tao F, He X, Zhang F, Arnoult C, Ray PF, Cao Y, Coutton C.
Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse.
Hum Genet. 2021 Sep;140(9):1367-1377. doi: 10.1007/s00439-021-02313-z.

43. Lorès P, Kheraff ZE, Amiri-Yekta A, Whitfield M, Daneshipour A, Stouvenel L, Cazin C, Cavarocchi E, Coutton C, Llabador MA, Arnoult C, Thierry-Mieg N, Ferreux L, Patrat C, Hosseini SH, Mustapha SFB, Zouari R, Dulioust E, Ray PF, Touré A.
A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.
Hum Genet. 2021 Jul;140(7):1031-1043. doi: 10.1007/s00439-021-02270-7.

42. Cazin C, Boumerdassi Y, Martinez G, Fourati Ben Mustapha S, Whitfield M, Coutton C, Thierry-Mieg N, Di Pizio P, Rives N, Arnoult C, Touré A, Ray PF, Zouari R, Sifer C, Kherraf ZE.
Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa.
Int J Mol Sci. 2021 Feb 22;22(4):2187. pdf. Full text online.

41. Arafah K, Lopez F, Cazin C, Kherraf ZE, Tassistro V, Loundou A, Arnoult C, Thierry-Mieg N, Bulet P, Guichaoua MR, Ray PF.
Defect in the nuclear pore membrane glycoprotein 210-like gene is associated with extreme uncondensed sperm nuclear chromatin and male infertility: a case report.
Hum Reprod. 2021 Feb 18;36(3):693-701.

40. Cavarocchi E, Whitfield M, Chargui A, Stouvenel L, Lorès P, Coutton C, Arnoult C, Santulli P, Patrat C, Thierry-Mieg N, Ray PF, Dulioust E, Touré A.
The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility.
Clin Genet. 2021 May;99(5):684-693. doi: 10.1111/cge.13927.

39. Celse T, Cazin C, Mietton F, Martinez G, Martinez D, Thierry-Mieg N, Septier A, Guillemain C, Beurois J, Clergeau A, Mustapha SFB, Kharouf M, Zoghmar A, Chargui A, Papaxanthos A, Dorphin B, Foliguet B, Triki C, Sifer C, Lauton D, Tachdjian G, Schuler G, Lejeune H, Puechberty J, Bessonnat J, Pasquier L, Mery L, Poulain M, Chaabouni M, Sermondade N, Cabry R, Benbouhadja S, Veau S, Frapsauce C, Mitchell V, Achard V, Satre V, Hennebicq S, Zouari R, Arnoult C, Kherraf ZE, Coutton C, Ray PF.
Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player.
Hum Genet. 2021 Jan;140(1):43-57.

38. Martinez G, Beurois J, Dacheux D, Cazin C, Bidart M, Kherraf ZE, Robinson DR, Satre V, Le Gac G, Ka C, Gourlaouen I, Fichou Y, Petre G, Dulioust E, Zouari R, Thierry-Mieg N, Touré A, Arnoult C, Bonhivers M, Ray P, Coutton C.
Biallelic variants in MAATS1 encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertility.
J Med Genet. 2020 Oct;57(10):708-716. pdf.

37. Beurois J, Martinez G, Cazin C, Kherraf ZE, Amiri-Yekta A, Thierry-Mieg N, Bidart M, Petre G, Satre V, Brouillet S, Touré A, Arnoult C, Ray PF, Coutton C.
CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case report.
Hum Reprod. 2019 Oct 2;34(10):2071-2079.

36. Kherraf ZE, Cazin C, Coutton C, Amiri-Yekta A, Martinez G, Boguenet M, Fourati Ben Mustapha S, Kharouf M, Gourabi H, Hosseini SH, Daneshipour A, Touré A, Thierry-Mieg N, Zouari R, Arnoult C, Ray PF.
Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations.
Clin Genet. 2019 Nov;96(5):394-401. pdf.

35. Coutton C, Martinez G, Kherraf ZE, Amiri-Yekta A, Boguenet M, Saut A, He X, Zhang F, Cristou-Kent M, Escoffier J, Bidart M, Satre V, Conne B, Fourati Ben Mustapha S, Halouani L, Marrakchi O, Makni M, Latrous H, Kharouf M, Pernet-Gallay K, Bonhivers M, Hennebicq S, Rives N, Dulioust E, Touré A, Gourabi H, Cao Y, Zouari R, Hosseini SH, Nef S, Thierry-Mieg N, Arnoult C, Ray PF.
Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice.
Am J Hum Genet. 2019 Feb 7;104(2):331-340. pdf.

34. Clerc O, Deniaud M, Vallet SD, Naba A, Rivet A, Perez S, Thierry-Mieg N*, Ricard-Blum S* (*: corresponding authors).
MatrixDB: integration of new data with a focus on glycosaminoglycan interactions.
Nucleic Acids Res. 2019 Jan 8;47(D1):D376-D381. pdf. Full text online.

33. Martinez G, Kherraf ZE, Zouari R, Fourati Ben Mustapha S, Saut A, Pernet-Gallay K, Bertrand A, Bidart M, Hograindleur JP, Amiri-Yekta A, Kharouf M, Karaouzène T, Thierry-Mieg N, Dacheux-Deschamps D, Satre V, Bonhivers M, Touré A, Arnoult C, Ray PF, Coutton C.
Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella.
Hum Reprod. 2018 Oct 1;33(10):1973-1984. pdf.

32. Kherraf ZE, Amiri-Yekta A, Dacheux D, Karaouzène T, Coutton C, Christou-Kent M, Martinez G, Landrein N, Le Tanno P, Fourati Ben Mustapha S, Halouani L, Marrakchi O, Makni M, Latrous H, Kharouf M, Pernet-Gallay K, Gourabi H, Robinson DR, Crouzy S, Blum M, Thierry-Mieg N, Touré A, Zouari R, Arnoult C, Bonhivers M, Ray PF.
A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility.
Am J Hum Genet. 2018 Sep 6;103(3):400-412. pdf. Full text online.

31. Christou-Kent M, Kherraf ZE, Amiri-Yekta A, Le Blévec E, Karaouzène T, Conne B, Escoffier J, Assou S, Guttin A, Lambert E, Martinez G, Boguenet M, Fourati Ben Mustapha S, Cedrin Durnerin I, Halouani L, Marrakchi O, Makni M, Latrous H, Kharouf M, Coutton C, Thierry-Mieg N, Nef S, Bottari SP, Zouari R, Issartel JP, Ray PF, Arnoult C.
PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice.
EMBO Mol Med. 2018 May;10(5). pii: e8515. pdf. Full text online.

30. Sivade Dumousseau M, Alonso-López D, Ammari M, Bradley G, Campbell NH, Ceol A, Cesareni G, Combe C, De Las Rivas J, Del-Toro N, Heimbach J, Hermjakob H, Jurisica I, Koch M, Licata L, Lovering RC, Lynn DJ, Meldal BHM, Micklem G, Panni S, Porras P, Ricard-Blum S, Roechert B, Salwinski L, Shrivastava A, Sullivan J, Thierry-Mieg N, Yehudi Y, Van Roey K, Orchard S.
Encompassing new use cases - level 3.0 of the HUPO-PSI format for molecular interactions.
BMC Bioinformatics. 2018 Apr 11;19(1):134. pdf. Full text online.

29. Dong FN, Amiri-Yekta A, Martinez G, Saut A, Tek J, Stouvenel L, Lorès P, Karaouzène T, Thierry-Mieg N, Satre V, Brouillet S, Daneshipour A, Hosseini SH, Bonhivers M, Gourabi H, Dulioust E, Arnoult C, Touré A, Ray PF, Zhao H, Coutton C.
Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse.
Am J Hum Genet. 2018 Apr 5;102(4):636-648. pdf. Full text online.

28. Coutton C, Vargas AS, Amiri-Yekta A, Kherraf ZE, Ben Mustapha SF, Le Tanno P, Wambergue-Legrand C, Karaouzène T, Martinez G, Crouzy S, Daneshipour A, Hosseini SH, Mitchell V, Halouani L, Marrakchi O, Makni M, Latrous H, Kharouf M, Deleuze JF, Boland A, Hennebicq S, Satre V, Jouk PS, Thierry-Mieg N, Conne B, Dacheux D, Landrein N, Schmitt A, Stouvenel L, Lorès P, El Khouri E, Bottari SP, Fauré J, Wolf JP, Pernet-Gallay K, Escoffier J, Gourabi H, Robinson DR, Nef S, Dulioust E, Zouari R, Bonhivers M, Touré A, Arnoult C, Ray PF.
Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human.
Nat Commun. 2018 Feb 15;9(1):686. pdf. Full text online.

27. Touat-Todeschini L, Shichino Y, Dangin M, Thierry-Mieg N, Gilquin B, Hiriart E, Sachidanandam R, Lambert E, Brettschneider J, Reuter M, Kadlec J, Pillai R, Yamashita A, Yamamoto M, Verdel A.
Selective termination of lncRNA transcription promotes heterochromatin silencing and cell differentiation.
EMBO J. 2017 Sep 1;36(17):2626-2641. pdf.

26. Vallet S, Deddens L, Vonarburg A, Salza R, Faye C, Aranyos A, Thierry-Mieg N, Ricard-Blum S.
Strategies for Building Protein–Glycosaminoglycan Interaction Networks Combining SPRi, SPR, and BLI.
Chapter 11 of the Handbook of Surface Plasmon Resonance (2), 2017, 398-414. pdf.

25. Kherraf ZE, Christou-Kent M, Karaouzene T, Amiri-Yekta A, Martinez G, Vargas AS, Lambert E, Borel C, Dorphin B, Aknin-Seifer I, Mitchell MJ, Metzler-Guillemain C, Escoffier J, Nef S, Grepillat M, Thierry-Mieg N, Satre V, Bailly M, Boitrelle F, Pernet-Gallay K, Hennebicq S, Fauré J, Bottari SP, Coutton C, Ray PF, Arnoult C.
SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes.
EMBO Mol Med. 2017 Aug, 9:1132-49. pdf. Full text online.

24. Escoffier J, Lee HC, Yassine S, Zouari R, Martinez G, Karaouzène T, Coutton C, Kherraf ZE, Halouani L, Triki C, Nef S, Thierry-Mieg N, Savinov SN, Fissore R, Ray PF, Arnoult C.
Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP.
Hum Mol Genet. 2016 Mar 1;25(5):878-91. pdf

23. Erlich Y, Gilbert A, Ngo H, Rudra A, Thierry-Mieg N, Wootters M, Zielinski D, Zuk O.
Biological screens from linear codes: theory and tools.
BioRxiv 2015 Dec 25; doi:10.1101/035352. pdf

22. Launay G, Salza R, Multedo D, Thierry-Mieg N, Ricard-Blum S.
MatrixDB, the extracellular matrix interaction database: updated content, a new navigator and expanded functionalities.
Nucleic Acids Res. 2015 Jan 28;43(Database issue):D321-7. pdf

21. Ben Khelifa M, Coutton C, Zouari R, Karaouzene T, Rendu J, Bidart M, Yassine S, Pierre V, Delaroche J, Hennebicq S, Grunwald D, Escalier D, Pernet-Gallay K, Jouk PS, Thierry-Mieg N, Toure A, Arnoult C, Ray PF.
Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella.
Am J Hum Genet. 2014 Jan; 94(1):95-104. pdf

20. Coutton C, Abada F, Karaouzene T, Sanlaville D, Satre V, Lunardi J, Jouk PS, Arnoult C, Thierry-Mieg N, Ray PF.
Fine Characterisation of a Recombination Hotspot at the DPY19L2 Locus and Resolution of the Paradoxical Excess of Duplications over Deletions in the General Population.
PLoS Genet. 2013 Mar;9(3):e1003363. Pubmed. pdf

19. Carvunis AR, Rolland T, Wapinski I, Calderwood MA, Yildirim MA, Simonis N, Charloteaux B, Hidalgo CA, Barbette J, Santhanam B, Brar GA, Weissman JS, Regev A, Thierry-Mieg N, Cusick ME, Vidal M.
Proto-genes and de novo gene birth.
Nature. 2012 Jul 19;487(7407):370-4. pdf

18. Xin X, Boone C, Thierry-Mieg N.
Mapping interactomes with high coverage and efficiency using the shifted transversal design.
Methods Mol Biol. 2012;812:147-59. pdf

17. Chautard E, Fatoux-Ardore M, Ballut L, Thierry-Mieg N, Ricard-Blum S.
MatrixDB, the extracellular matrix interaction database.
Nucleic Acids Res. 2011 Jan;39(Database issue):D235-40. pdf

16. Sambourg L, Thierry-Mieg N* (*: corresponding author).
New insights into protein-protein interaction data lead to increased estimates of the S. cerevisiae interactome size.
BMC Bioinformatics. 2010 Dec 21;11:605. Get the pdf on the BMC website or read it online.

15. Chautard E, Thierry-Mieg N, Ricard-Blum S.
Interaction networks as a tool to investigate the mechanisms of aging.
Biogerontology. 2010 Aug;11(4):463-73. Epub 2010 Mar 7. pdf

14. Carvunis AR, Gomez E, Thierry-Mieg N, Trilling L, Vidal M.
Systems biology: from yesterday's concepts to tomorrow's discoveries [Article in French].
Med Sci (Paris). 2009 Jun-Jul;25(6-7):578-84. pdf

13. Xin X*, Rual JF, Hirozane-Kishikawa T, Hill DE, Vidal M+, Boone C+, Thierry-Mieg N+* (*: contributed equally; +: corresponding authors).
Shifted Transversal Design smart-pooling for high coverage interactome mapping.
Genome Res. 2009 Jul;19(7):1262-9. Epub 2009 May 15. pdf (the Supp Data file is also available on my smart-pooling page).

12. Sultan A, Strodthoff D, Robertson AK, Paulsson-Berne G, Fauconnier J, Parini P, Ryden M, Thierry-Mieg N, Johansson ME, Chibalin AV, Zierath JR, Arner P, Hansson GK.
T cell-mediated inflammation in adipose tissue does not cause insulin resistance in hyperlipidemic mice.
Circ Res. 2009 Apr 24;104(8):961-8. Epub 2009 Mar 19. pdf

11. Chautard E, Ballut L, Thierry-Mieg N*, Ricard-Blum S* (*: corresponding authors).
MatrixDB, a database focused on extracellular protein-protein and protein-carbohydrate interactions.
Bioinformatics. 2009 Mar 1;25(5):690-1. Epub 2009 Jan 15. pdf

10. Chautard E, Thierry-Mieg N, Ricard-Blum S.
Interaction networks: From protein functions to drug discovery. A review.
Pathol Biol (Paris). 2009 Jun;57(4):324-33. Epub 2008 Dec 13. pdf

9. Schliep A, Shokrollahi A, Thierry-Mieg N (editors).
Dagstuhl Seminar 08301 Report: Group Testing in the Life Sciences.
Dagstuhl Seminar Proceedings, July 2008, Schloss Dagstuhl - Leibniz-Zentrum fuer Informatik, Germany.
Seminar homepage.

8. Thierry-Mieg N*, Bailly G (*: corresponding author).
Interpool: interpreting smart-pooling results.
Bioinformatics. 2008 Mar 1; 24(5):696-703. pdf

7. Thierry-Mieg N.
Pooling in systems biology becomes smart.
Nat Methods. 2006 Mar; 3(3):161-2. pdf

6. Thierry-Mieg N.
A new pooling strategy for high-throughput screening: the Shifted Transversal Design.
BMC Bioinformatics. 2006 Jan 19; 7:28. pdf

5. Davy A, Bello P, Thierry-Mieg N, Vaglio P, Hitti J, Doucette-Stamm L, Thierry-Mieg D, Reboul J, Boulton S, Walhout AJ, Coux O, Vidal M.
A protein-protein interaction map of the Caenorhabditis elegans 26S proteasome.
EMBO Rep. 2001 Sep; 2(9):821-8.

4. Reboul J, Vaglio P, Tzellas N, Thierry-Mieg N, Moore T, Jackson C, Shin-i T, Kohara Y, Thierry-Mieg D, Thierry-Mieg J, Lee H, Hitti J, Doucette-Stamm L, Hartley JL, Temple GF, Brasch MA, Vandenhaute J, Lamesch PE, Hill DE, Vidal M.
Open-reading-frame sequence tags (OSTs) support the existence of at least 17,300 genes in C. elegans.
Nat Genet. 2001 Mar; 27(3):332-6.

3. Thierry-Mieg N*, Trilling L* (*: corresponding authors).
InterDB, a Prediction-Oriented Protein Interaction Database for C. elegans.
In O. Gascuel M.F. Sagot eds., JOBIM 2000 selected papers, Lecture Notes in Computer Science (2001), 2066, 135-146. pdf

2. Walhout AJ, Sordella R, Lu X, Hartley JL, Temple GF, Brasch MA, Thierry-Mieg N, Vidal M.
Protein interaction mapping in C. elegans using proteins involved in vulval development.
Science. 2000 Jan 7; 287(5450):116-22.

1. Walhout M, Endoh H, Thierry-Mieg N, Wong W, Vidal M.
A model of elegance.
Am J Hum Genet. 1998 Oct; 63(4):955-61.

Last modified 03/07/2024