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Suggested authors matching "AUTH:Leroux D" with an ORCID

Delphine Leroux
Centre National de Recherches Météorologiques
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Classification of <i>PTEN</i> germline non-truncating variants: a new approach to interpretation.
Margot H, Jones N, Matis T, Bonneau D, Busa T, Bonnet F, Conrad S, Crivelli L, Monin P, Fert-Ferrer S, Mortemousque I, Raad S, Lacombe D, Caux F, Sevenet N, Bubien V, Longy M, French Cowden Disease Network
J Med Genet, jmg-2024-109982, 02 Oct 2024
Cited by: 0 articles | PMID: 39358013
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Together4RD position statement on collaboration between European reference networks and industry.
Hedley V, Bolz-Johnson M, Hernando I, Kenward R, Nabbout R, Romero C, Schaefer F, Upadhyaya S, Together4RD Steering Group
Orphanet J Rare Dis, 18(1):272, 05 Sep 2023
Cited by: 1 article | PMID: 37670358 | PMCID: PMC10478454
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Clinical features and long-term outcomes of patients with systemic polyarteritis nodosa diagnosed since 2005: Data from 196 patients.
Rohmer J, Nguyen Y, Trefond L, Agard C, Allain JS, Berezne A, Charles P, Cohen P, Gondran G, Groh M, Huscenot T, Lacout C, Lazaro E, London J, Maurier F, Mekinian A, Mesbah R, Nubourgh I, Perard L, [...] French Vasculitis Study Group (FVSG)
J Autoimmun, 139:103093, 01 Aug 2023
Cited by: 5 articles | PMID: 37536165
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Current Management of Patients with RPE65 Mutation Associated Inherited Retinal Degenerations in Europe: Results of a 2-Year Follow-Up Multinational Survey.
Lorenz B, Tavares J, van den Born LI, Marques JP, Pilotto E, Stingl K, Charbel Issa P, Leroux D, Dollfus H, Scholl HPN
Ophthalmic Res, 66(1):727-748, 06 Mar 2023
Cited by: 3 articles | PMID: 36878196
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Current Management of Inherited Retinal Degeneration Patients in Europe: Results of a 2-Year Follow-Up Multinational Survey by the European Vision Institute Clinical Research Network - EVICR.net.
Lorenz B, Tavares J, van den Born LI, Marques JP, Pilotto E, Stingl K, Charbel Issa P, Leroux D, Dollfus H, Scholl HPN, EVICR.net study group, ERN-EYE study group
Ophthalmic Res, 66(1):550-568, 02 Jan 2023
Cited by: 2 articles | PMID: 36592621
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SeSAM: software for automatic construction of order-robust linkage maps.
Vidal A, Gauthier F, Rodrigez W, Guiglielmoni N, Leroux D, Chevrolier N, Jasson S, Tourrette E, Martin OC, Falque M
BMC Bioinformatics, 23(1):499, 19 Nov 2022
Cited by: 0 articles | PMID: 36402957 | PMCID: PMC9675223
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Low-dose interleukin-2 therapy in active systemic lupus erythematosus (LUPIL-2): a multicentre, double-blind, randomised and placebo-controlled phase II trial.
Humrich JY, Cacoub P, Rosenzwajg M, Pitoiset F, Pham HP, Guidoux J, Leroux D, Vazquez T, Riemekasten G, Smolen JS, Tsokos G, Klatzmann D
Ann Rheum Dis, 81(12):1685-1694, 16 Aug 2022
Cited by: 32 articles | PMID: 35973803
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Toxic stress and disconnection from work and school among youth in Detroit.
Camp JK, Hall TS, Chua JC, Ralston KG, Leroux DF, Belgrade A, Shattuck S
J Community Psychol, 50(2):876-895, 20 Aug 2021
Cited by: 1 article | PMID: 34415619
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A new hybrid record linkage process to make epidemiological databases interoperable: application to the GEMO and GENEPSO studies involving BRCA1 and BRCA2 mutation carriers.
Jiao Y, Lesueur F, Azencott CA, Laurent M, Mebirouk N, Laborde L, Beauvallet J, Dondon MG, Eon-Marchais S, Laugé A, GEMO Study Collaborators, GENEPSO Study Collaborators, Noguès C, Andrieu N, Stoppa-Lyonnet D, Caputo SM
BMC Med Res Methodol, 21(1):155, 29 Jul 2021
Cited by: 2 articles | PMID: 34325649 | PMCID: PMC8320036
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Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
Coignard J, Lush M, Beesley J, O'Mara TA, Dennis J, Tyrer JP, Barnes DR, McGuffog L, Leslie G, Bolla MK, Adank MA, Agata S, Ahearn T, Aittomäki K, Andrulis IL, Anton-Culver H, Arndt V, Arnold N, Aronson KJ, [...] Antoniou AC
Nat Commun, 12(1):2986, 14 May 2021
Cited by: 0 articles | PMID: 33990587 | PMCID: PMC8121813
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The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant.
Lakeman IMM, van den Broek AJ, Vos JAM, Barnes DR, Adlard J, Andrulis IL, Arason A, Arnold N, Arun BK, Balmaña J, Barrowdale D, Benitez J, Borg A, Caldés T, Caligo MA, Chung WK, Claes KBM, GEMO Study Collaborators, EMBRACE Collaborators, [...] Schmidt MK
Genet Med, 23(9):1726-1737, 10 Jun 2021
Cited by: 11 articles | PMID: 34113011 | PMCID: PMC8460445
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The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement.
Black GC, Sergouniotis P, Sodi A, Leroy BP, Van Cauwenbergh C, Liskova P, Grønskov K, Klett A, Kohl S, Taurina G, Sukys M, Haer-Wigman L, Nowomiejska K, Marques JP, Leroux D, Cremers FPM, De Baere E, Dollfus H, ERN-EYE study group
Orphanet J Rare Dis, 16(1):142, 20 Mar 2021
Cited by: 17 articles | PMID: 33743793 | PMCID: PMC7980559
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Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study.
Schrijver LH, Antoniou AC, Olsson H, Mooij TM, Roos-Blom MJ, Azarang L, Adlard J, Ahmed M, Barrowdale D, Davidson R, Donaldson A, Eeles R, Evans DG, Frost D, Henderson A, Izatt L, Ong KR, Bonadona V, Coupier I, [...] and International BRCA1/2 Carrier Cohort Study
Am J Obstet Gynecol, 225(1):51.e1-51.e17, 22 Jan 2021
Cited by: 24 articles | PMID: 33493488 | PMCID: PMC8278569
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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
Coignard J, Lush M, Beesley J, O'Mara TA, Dennis J, Tyrer JP, Barnes DR, McGuffog L, Leslie G, Bolla MK, Adank MA, Agata S, Ahearn T, Aittomäki K, Andrulis IL, Anton-Culver H, Arndt V, Arnold N, Aronson KJ, [...] Antoniou AC
Nat Commun, 12(1):1078, 17 Feb 2021
Cited by: 17 articles | PMID: 33597508 | PMCID: PMC7890067
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National recommendations of the French Genetics and Cancer Group - Unicancer on the modalities of multi-genes panel analyses in hereditary predispositions to tumors of the digestive tract.
Dhooge M, Baert-Desurmont S, Corsini C, Caron O, Andrieu N, Berthet P, Bonadona V, Cohen-Haguenauer O, De Pauw A, Delnatte C, Dussart S, Lasset C, Leroux D, Maugard C, Moretta-Serra J, Popovici C, Buecher B, Colas C, Noguès C, GGC-Unicancer Group
Eur J Med Genet, 63(12):104080, 08 Oct 2020
Cited by: 4 articles | PMID: 33039684
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Transcriptome-wide association study of breast cancer risk by estrogen-receptor status.
Feng H, Gusev A, Pasaniuc B, Wu L, Long J, Abu-Full Z, Aittomäki K, Andrulis IL, Anton-Culver H, Antoniou AC, Arason A, Arndt V, Aronson KJ, Arun BK, Asseryanis E, Auer PL, Azzollini J, Balmaña J, Barkardottir RB, [...] Jiang X
Genet Epidemiol, 44(5):442-468, 01 Mar 2020
Cited by: 26 articles | PMID: 32115800 | PMCID: PMC7987299
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Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers.
Mavaddat N, Antoniou AC, Mooij TM, Hooning MJ, Heemskerk-Gerritsen BA, GENEPSO, Noguès C, Gauthier-Villars M, Caron O, Gesta P, Pujol P, Lortholary A, EMBRACE, Barrowdale D, Frost D, Evans DG, Izatt L, Adlard J, Eeles R, [...] BCFR
Breast Cancer Res, 22(1):8, 16 Jan 2020
Cited by: 30 articles | PMID: 31948486 | PMCID: PMC6966793
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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.
Fachal L, Aschard H, Beesley J, Barnes DR, Allen J, Kar S, Pooley KA, Dennis J, Michailidou K, Turman C, Soucy P, Lemaçon A, Lush M, Tyrer JP, Ghoussaini M, Moradi Marjaneh M, Jiang X, Agata S, Aittomäki K, [...] Dunning AM
Nat Genet, 52(1):56-73, 07 Jan 2020
Cited by: 91 articles | PMID: 31911677 | PMCID: PMC6974400
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Supporting caregivers of children born prematurely in the development of language: A scoping review.
Belanger R, Leroux D, Lefebvre P
Paediatr Child Health, 26(1):e17-e24, 21 Oct 2019
Cited by: 2 articles | PMID: 33542775 | PMCID: PMC7850271
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When pictures take away from the message: An examination of young adults' attention to texting and driving advertisements.
Foglia V, Roy-Charland A, Leroux D, Lemieux S, Yantzi N, Skjonsby-McKinnon T, Fiset S, Guitard D
Can J Exp Psychol, 74(2):131-143, 14 Oct 2019
Cited by: 1 article | PMID: 31613130
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Osteosarcoma without prior retinoblastoma related to RB1 low-penetrance germline pathogenic variants: A novel type of RB1-related hereditary predisposition syndrome?
Imbert-Bouteille M, Gauthier-Villars M, Leroux D, Meunier I, Aerts I, Lumbroso-Le Rouic L, Lejeune S, Delnatte C, Abadie C, Pujol P, Houdayer C, Corsini C
Mol Genet Genomic Med, 7(12):e913, 30 Sep 2019
Cited by: 7 articles | PMID: 31568710 | PMCID: PMC6900371
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Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers.
Qian F, Rookus MA, Leslie G, Risch HA, Greene MH, Aalfs CM, Adank MA, Adlard J, Agnarsson BA, Ahmed M, Aittomäki K, Andrulis IL, Arnold N, Arun BK, Ausems MGEM, Azzollini J, Barrowdale D, Barwell J, Benitez J, [...] CIMBA
Br J Cancer, 121(2):180-192, 19 Jun 2019
Cited by: 10 articles | PMID: 31213659 | PMCID: PMC6738050
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Correction to: An ontological foundation for ocular phenotypes and rare eye diseases.
Sergouniotis PI, Maxime E, Leroux D, Olry A, Thompson R, Rath A, Robinson PN, Dollfus H, ERN-EYE Ontology Study Group
Orphanet J Rare Dis, 14(1):200, 15 Aug 2019
Cited by: 0 articles | PMID: 31416457 | PMCID: PMC6696684
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Congenital Rubella Syndrome Surveillance in South Africa Using a Sentinel Site Approach: A Cross-sectional Study.
Motaze NV, Manamela J, Smit S, Rabie H, Harper K, duPlessis N, Reubenson G, Coetzee M, Ballot D, Moore D, Nuttall J, Linley L, Tooke L, Kriel J, Hallbauer U, Sutton C, Moodley P, Hardie D, Mazanderani AH, [...] Suchard M
Clin Infect Dis, 68(10):1658-1664, 01 May 2019
Cited by: 8 articles | PMID: 30203002 | PMCID: PMC6495013
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Endoscopic Phenotype of Monoallelic Carriers of MUTYH Gene Mutations in the Family of Polyposis Patients: A Prospective Study.
El Hachem N, Abadie C, Longy M, Colas C, Fert-Ferrer S, Leroux D, Grandval P, Prieur F, Collonge-Rame M, Faivre L, Fricker JP, Zerbib F, Coupier I, Cauchin E, Pinson S, Saurin JC
Dis Colon Rectum, 62(4):470-475, 01 Apr 2019
Cited by: 3 articles | PMID: 30640315
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