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authIdHal_s : nthierry
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New insights into protein-protein interaction data lead to increased estimates of the S. cerevisiae interactome size.

Laure Sambourg , Nicolas Thierry-Mieg
BMC Bioinformatics, 2010, 11, pp.605. ⟨10.1186/1471-2105-11-605⟩
Journal articles hal-00807360v1
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MatrixDB: integration of new data with a focus on glycosaminoglycan interactions

Olivier Clerc , Madeline Deniaud , Sylvain Vallet , Alexandra Naba , Alain Rivet et al.
Nucleic Acids Research, 2019, 47 (D1), pp.D376-D381. ⟨10.1093/nar/gky1035⟩
Journal articles hal-02109904v1

Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations

Zine‐eddine Kherraf , Caroline Cazin , Charles Coutton , Amir Amiri‐yekta , Guillaume Martinez et al.
Clinical Genetics, 2019, 96 (5), pp.394-401. ⟨10.1111/cge.13604⟩
Journal articles hal-02347512v1
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The [PSI+] prion and HSP104 modulate cytochrome c oxidase deficiency caused by deletion of COX12

Pawan Kumar Saini , Hannah Dawitz , Andreas Aufschnaiter , Jinsu Thomas , Amélie Amblard et al.
Preprints, Working Papers, ... hal-03402829v1

A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility.

Zine-Eddine Kherraf , Amir Amiri-Yekta , Denis Dacheux , Thomas Karaouzène , Charles Coutton et al.
American Journal of Human Genetics, 2018, 103 (3), pp.400-412. ⟨10.1016/j.ajhg.2018.07.014⟩
Journal articles hal-01863586v1
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New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella

Guillaume Martinez , Anne-Laure Barbotin , Caroline Cazin , Zeina Wehbe , Angèle Boursier et al.
International Journal of Molecular Sciences, 2023, 24 (3), pp.2559. ⟨10.3390/ijms24032559⟩
Journal articles hal-04011973v1
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From azoospermia to macrozoospermia, a phenotypic continuum due to mutations in the ZMYND15 gene

Zine-Eddine Kherraf , Caroline Cazin , Florence Lestrade , Jana Muronova , Charles Coutton et al.
Asian Journal of Andrology, 2022, 24 (3), pp.243-247. ⟨10.4103/aja202194⟩
Journal articles hal-03720221v1
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A new pooling strategy for high-throughput screening: the Shifted Transversal Design.

Nicolas Thierry-Mieg
BMC Bioinformatics, 2006, 7, pp.28. ⟨10.1186/1471-2105-7-28⟩
Journal articles hal-00198315v1
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CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia.

Julie Beurois , Guillaume Martinez , Caroline Cazin , Zine-Eddine Kherraf , Amir Amiri-Yekta et al.
Human Reproduction, 2019, 96 (5), pp.394-401. ⟨10.1093/humrep/dez166⟩
Journal articles hal-02322935v1
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Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player

Tristan Celse , Caroline Cazin , Flore Mietton , Guillaume Martinez , Delphine Martinez et al.
Human Genetics, 2021, Molecular Genetics of Male Infertility, 140 (1), pp.43-57. ⟨10.1007/s00439-020-02229-0⟩
Journal articles hal-03025179v1
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Biallelic variants in MAATS1 encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertility

Guillaume Martinez , Julie Beurois , Denis Dacheux , Caroline Cazin , Marie Bidart et al.
Journal of Medical Genetics, 2020, 57 (10), pp.708-716. ⟨10.1136/jmedgenet-2019-106775⟩
Journal articles hal-03004959v1
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PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice

Marie Christou‐kent , Zine‐eddine Kherraf , Amir Amiri‐yekta , Emilie Le Blévec , Thomas Karaouzène et al.
EMBO Molecular Medicine, 2018, 10 (5), pp.e8515. ⟨10.15252/emmm.201708515⟩
Journal articles hal-01877992v1

Mapping interactomes with high coverage and efficiency using the shifted transversal design.

Xiaofeng Xin , Charles Boone , Nicolas Thierry-Mieg
Methods in Molecular Biology, 2012, 812, pp.147-59. ⟨10.1007/978-1-61779-455-1_8⟩
Journal articles hal-00807350v1
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Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella.

Mariem Ben Khelifa , Charles Coutton , Raoudha Zouari , Thomas Karaouzène , John Rendu et al.
American Journal of Human Genetics, 2014, 94 (1), pp.95-104. ⟨10.1016/j.ajhg.2013.11.017⟩
Journal articles pasteur-01061012v1

Pooling in systems biology becomes smart.

Nicolas Thierry-Mieg
Nature Methods, 2006, 3 (3), pp.161-2. ⟨10.1038/nmeth0306-161⟩
Journal articles hal-00198318v1

Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse

Frederick Dong , Amir Amiri-Yekta , Guillaume Martinez , Antoine Saut , Julie Tek et al.
American Journal of Human Genetics, 2018, 102 (4), pp.636 - 648. ⟨10.1016/j.ajhg.2018.03.007⟩
Journal articles hal-01877985v1

Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP

Jessica Escoffier , Hoi Chang Lee , Sandra Yassine , Raoudha Zouari , Guillaume Martinez et al.
Human Molecular Genetics, 2016, 25 (5), pp.878 - 891. ⟨10.1093/hmg/ddv617⟩
Journal articles hal-01877966v1

Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in $Trypanosoma$ and human.

Charles Coutton , Alexandra S. Vargas , Amir Amiri-Yekta , Zine-Eddine Kherraf , Selima Fourati Ben Mustapha et al.
Nature Communications, 2018, 9, pp.686. ⟨10.1038/s41467-017-02792-7⟩
Journal articles hal-01724640v1
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Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa

Caroline Cazin , Yasmine Boumerdassi , Guillaume Martinez , Selima Fourati Ben Mustapha , Marjorie Whitfield et al.
International Journal of Molecular Sciences, 2021, 22 (4), pp.2187. ⟨10.3390/ijms22042187⟩
Journal articles hal-03365058v1

MatrixDB, the extracellular matrix interaction database.

Emilie Chautard , Marie Fatoux-Ardore , Lionel Ballut , Nicolas Thierry-Mieg , Sylvie Ricard-Blum et al.
Nucleic Acids Research, 2011, 39 (Database issue), pp.D235-40. ⟨10.1093/nar/gkq830⟩
Journal articles hal-00807349v1
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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

Patrick Lorès , Zine-Eddine Kherraf , Amir Amiri-Yekta , Marjorie Whitfield , Abbas Daneshipour et al.
Human Genetics, 2021, 140 (7), pp.1031-1043. ⟨10.1007/s00439-021-02270-7⟩
Journal articles hal-03369854v1
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The [PSI + ] prion modulates cytochrome c oxidase deficiency caused by deletion of COX12

Pawan Kumar Saini , Hannah Dawitz , Andreas Aufschnaiter , Stanislav Bondarev , Jinsu Thom et al.
Molecular Biology of the Cell, 2022, ⟨10.1091/mbc.E21-10-0499⟩
Journal articles hal-03836554v1
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Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermia

Zine-Eddine Kherraf , Caroline Cazin , Amine Bouker , Selima Fourati Ben Mustapha , Sylviane Hennebicq et al.
American Journal of Human Genetics, 2022, 109 (3), pp.508-517. ⟨10.1016/j.ajhg.2022.01.011⟩
Journal articles hal-03718022v1

Interpool: interpreting smart-pooling results

Nicolas Thierry-Mieg , Gilles Bailly
Bioinformatics, 2008, 24 (5), pp.696 - 703. ⟨10.1093/bioinformatics/btn001⟩
Journal articles hal-01894176v1

Systems biology: from yesterday's concepts to tomorrow's discoveries

Anne-Ruxandra Carvunis , Elisa Gomez , Nicolas Thierry-Mieg , Laurent Trilling , Marc Vidal et al.
médecine/sciences, 2009, 25 (6-7), pp.578-584. ⟨10.1051/medsci/2009256-7578⟩
Journal articles hal-03266023v1
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The sodium/proton exchanger SLC9C1 ( sNHE ) is essential for human sperm motility and fertility

Emma Cavarocchi , Marjorie Whitfield , Ahmed Chargui , Laurence Stouvenel , Patrick Lorès et al.
Clinical Genetics, 2021, 99 (5), pp.684-693. ⟨10.1111/cge.13927⟩
Journal articles hal-03369825v1
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Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse

Qunshan Shen , Guillaume Martinez , Hongbin Liu , Julie Beurois , Huan Wu et al.
Human Genetics, 2021, 140 (9), pp.1367-1377. ⟨10.1007/s00439-021-02313-z⟩
Journal articles hal-03365264v1
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Defect in the nuclear pore membrane glycoprotein 210-like gene is associated with extreme uncondensed sperm nuclear chromatin and male infertility: a case report

Karim Arafah , Fabrice Lopez , Caroline Cazin , Zine‐eddine Kherraf , Virginie Tassistro et al.
Human Reproduction, 2021, 36 (3), pp.693-701. ⟨10.1093/humrep/deaa329⟩
Journal articles hal-02985525v1

Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella

Guillaume Martinez , Zine-Eddine Kherraf , Raoudha Zouari , Selima Fourati Ben Mustapha , Antoine Saut et al.
Human Reproduction, 2018, 33 (10), pp.1973 - 1984. ⟨10.1093/humrep/dey264⟩
Journal articles hal-01877993v1

Selective termination of lncRNA transcription promotes heterochromatin silencing and cell differentiation

Leila Touat‐todeschini , Yuichi Shichino , Mathieu Dangin , Nicolas Thierry-Mieg , Benoit Gilquin et al.
EMBO Journal, 2017, 36 (17), pp.2626 - 2641. ⟨10.15252/embj.201796571⟩
Journal articles hal-01877979v1