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Papers authored by Bonneau D

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Comparison of methods to assess quadriceps muscle volume using magnetic resonance imaging.

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Nordez A, Jolivet E, Südhoff I, Bonneau D, de Guise JA, and Skalli W

Journal of magnetic resonance imaging : JMRI 30(5):1116-23, 2009 Nov - Who cited this? | PubMed ID: 19856445 | Fulltext

OPA1-associated disorders: phenotypes and pathophysiology.

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Amati-Bonneau P, Milea D, Bonneau D, Chevrollier A, Ferré M, Guillet V, Gueguen N, Loiseau D, de Crescenzo MA, Verny C, Procaccio V, Lenaers G, and Reynier P

The international journal of biochemistry & cell biology 41(10):1855-65, 2009 Oct - Who cited this? | PubMed ID: 19389487 | Fulltext

Manifestations of pseudoxanthoma elasticum in childhood.

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Naouri M, Boisseau C, Bonicel P, Daudon P, Bonneau D, Chassaing N, and Martin L

The British journal of dermatology 161(3):635-9, 2009 Sep - Who cited this? | PubMed ID: 19519828 | Fulltext

Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.

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Ferré M, Bonneau D, Milea D, Chevrollier A, Verny C, Dollfus H, Ayuso C, Defoort S, Vignal C, Zanlonghi X, Charlin JF, Kaplan J, Odent S, Hamel CP, Procaccio V, Reynier P,

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Human mutation 30(7):E692-705, 2009 Jul - Who cited this? | PubMed ID: 19319978 | Fulltext

3D-patient-specific geometry of the muscles involved in knee motion from selected MRI images.

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Südhoff I, de Guise JA, Nordez A, Jolivet E, Bonneau D, Khoury V, and Skalli W

Medical & biological engineering & computing 47(6):579-87, 2009 Jun - Who cited this? | PubMed ID: 19277749 | Fulltext

Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).

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Cassereau J, Chevrollier A, Gueguen N, Malinge MC, Letournel F, Nicolas G, Richard L, Ferre M, Verny C, Dubas F, Procaccio V, Amati-Bonneau P, Bonneau D, and Reynier P

Neurogenetics 10(2):145-50, 2009 Apr - Who cited this? | PubMed ID: 19089472 | Fulltext

A large-scale mutation search reveals genetic heterogeneity in 3M syndrome.

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Huber C, Delezoide AL, Guimiot F, Baumann C, Malan V, Le Merrer M, Da Silva DB, Bonneau D, Chatelain P, Chu C, Clark R, Cox H, Edery P, Edouard T, Fano V, Gibson K,

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European journal of human genetics : EJHG 17(3):395-400, 2009 Mar - Who cited this? | PubMed ID: 19225462 | Fulltext

Surgical treatment for incessant pericarditis.

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Hota SS, Chow CM, Bonneau D, and Chisholm RJ

The Canadian journal of cardiology 25(3):161-2, 2009 Mar - Who cited this? | PubMed ID: 19279984 | Fulltext

Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defect.

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Nochez Y, Arsene S, Gueguen N, Chevrollier A, Ferré M, Guillet V, Desquiret V, Toutain A, Bonneau D, Procaccio V, Amati-Bonneau P, Pisella PJ, and Reynier P

Molecular vision 15:598-608, 2009 - Who cited this? | PubMed ID: 19325939 | Fulltext

Sternal plating for primary and secondary sternal closure; can it improve sternal stability?.

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Fawzy H, Alhodaib N, Mazer CD, Harrington A, Latter D, Bonneau D, Errett L, and Mahoney J

Journal of cardiothoracic surgery 4:19, 2009 - Who cited this? | PubMed ID: 19419587 | Fulltext

Can local application of Tranexamic acid reduce post-coronary bypass surgery blood loss? A randomized controlled trial.

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Fawzy H, Elmistekawy E, Bonneau D, Latter D, and Errett L

Journal of cardiothoracic surgery 4:25, 2009 - Who cited this? | PubMed ID: 19538741 | Fulltext

Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitis.

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Verny C, Amati-Bonneau P, Letournel F, Person B, Dib N, Malinge MC, Slama A, Le Maréchal C, Ferec C, Procaccio V, Reynier P, and Bonneau D

Diabetes & metabolism 34(6):620-6, 2008 Dec - Who cited this? | PubMed ID: 18955007 | Fulltext

Influence of ultrasonographers training on prenatal diagnosis of congenital heart diseases: a 12-year population-based study.

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Pézard P, Bonnemains L, Boussion F, Sentilhes L, Allory P, Lépinard C, Guichet A, Triau S, Biquard F, Leblanc M, Bonneau D, and Descamps P

Prenatal diagnosis, 2008 Oct 16 - Who cited this? | PubMed ID: 18925579 | Fulltext

Relationship between preventability of death after coronary artery bypass graft surgery and all-cause risk-adjusted mortality rates.

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Guru V, Tu JV, Etchells E, Anderson GM, Naylor CD, Novick RJ, Feindel CM, Rubens FD, Teoh K, Mathur A, Hamilton A, Bonneau D, Cutrara C, Austin PC, and Fremes SE

Circulation 117(23):2969-76, 2008 Jun 10 - Who cited this? | PubMed ID: 18541752 | Fulltext

Prognostic molecular markers with no impact on decision-making: the paradox of gliomas based on a prospective study.

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Wager M, Menei P, Guilhot J, Levillain P, Michalak S, Bataille B, Blanc JL, Lapierre F, Rigoard P, Milin S, Duthe F, Bonneau D, Larsen CJ, and Karayan-Tapon L

British journal of cancer 98(11):1830, 2008 Jun 3 - Who cited this? | PubMed ID: 18506188 | Fulltext

Molecular cytogenetic characterization of terminal 14q32 deletions in two children with an abnormal phenotype and corpus callosum hypoplasia.

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Schneider A, Benzacken B, Guichet A, Verloes A, Bonneau D, Collot N, Dastot-Le-Moal F, Goossens M, Taine L, Landais E, Gaillard D, and Doco-Fenzy M

European journal of human genetics : EJHG 16(6):680, 2008 Jun - Who cited this? | PubMed ID: 18197200 | Fulltext

Volumic patient-specific reconstruction of muscular system based on a reduced dataset of medical images.

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Jolivet E, Daguet E, Pomero V, Bonneau D, Laredo JD, and Skalli W

Computer methods in biomechanics and biomedical engineering 11(3):281-90, 2008 Jun - Who cited this? | PubMed ID: 18568825 | Fulltext

Hereditary optic neuropathies share a common mitochondrial coupling defect.

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Chevrollier A, Guillet V, Loiseau D, Gueguen N, de Crescenzo MA, Verny C, Eng MF, Dollfus H, Odent S, Milea D, Goizet C, Amati-Bonneau P, Procaccio V, Bonneau D, and Reynier P

Annals of neurology 63(6):794-8, 2008 Jun - Who cited this? | PubMed ID: 18496845 | Fulltext

Reversible optic neuropathy with OPA1 exon 5b mutation.

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Cornille K, Milea D, Amati-Bonneau P, Procaccio V, Zazoun L, Guillet V, El Achouri G, Delettre C, Gueguen N, Loiseau D, Muller A, Ferré M, Chevrollier A, Wallace DC, Bonneau D, Hamel C,

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Annals of neurology 63(5):667-71, 2008 May - Who cited this? | PubMed ID: 18360822 | Fulltext

Multiple sclerosis-like disorder in opa1-related autosomal dominant optic atrophy.

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Verny C, Loiseau D, Scherer C, Lejeune P, Chevrollier A, Gueguen N, Guillet V, Dubas F, Reynier P, Amati-Bonneau P, and Bonneau D

Neurology 70(13 Pt 2):1152-3, 2008 Mar 25 - Who cited this? | PubMed ID: 18287570 | Fulltext

Perrault syndrome: report of four new cases, review and exclusion of candidate genes.

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Marlin S, Lacombe D, Jonard L, Leboulanger N, Bonneau D, Goizet C, de Villemeur TB, Cabrol S, Houang M, Moatti L, Feldmann D, and Denoyelle F

American journal of medical genetics. Part A 146(5):661-4, 2008 Mar 1 - Who cited this? | PubMed ID: 18241061 | Fulltext

Heterozygosity for a single mutation in the ABCC6 gene may closely mimic PXE: consequences of this phenotype overlap for the definition of PXE.

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Martin L, Maître F, Bonicel P, Daudon P, Verny C, Bonneau D, Le Saux O, and Chassaing N

Archives of dermatology 144(3):301-6, 2008 Mar - Who cited this? | PubMed ID: 18347285 | Fulltext

Carotid artery dissection in an adult with the Simpson-Golabi-Behmel syndrome.

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Pénisson-Besnier I, Lebouvier T, Moizard MP, Ferré M, Barth M, Marc G, Raynaud M, and Bonneau D

American journal of medical genetics. Part A 146(4):464-7, 2008 Feb 15 - Who cited this? | PubMed ID: 18203194 | Fulltext

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes.

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Amati-Bonneau P, Valentino ML, Reynier P, Gallardo ME, Bornstein B, Boissière A, Campos Y, Rivera H, de la Aleja JG, Carroccia R, Iommarini L, Labauge P, Figarella-Branger D, Marcorelles P, Furby A, Beauvais K,

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Brain : a journal of neurology 131(Pt 2):338, 2008 Feb - Who cited this? | PubMed ID: 18158317 | Fulltext

Cognitive changes in asymptomatic carriers of the Huntington disease mutation gene.

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Verny C, Allain P, Prudean A, Malinge MC, Gohier B, Scherer C, Bonneau D, Dubas F, and Le Gall D

European journal of neurology : the official journal of the European Federation of Neurological Societies 14(12):1344-50, 2007 Dec - Who cited this? | PubMed ID: 17941857 | Fulltext

Heterogeneity of NSD1 alterations in 116 patients with Sotos syndrome.

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Saugier-Veber P, Bonnet C, Afenjar A, Drouin-Garraud V, Coubes C, Fehrenbach S, Holder-Espinasse M, Roume J, Malan V, Portnoi MF, Jeanne N, Baumann C, Héron D, David A, Gérard M, Bonneau D,

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Human mutation 28(11):1098-107, 2007 Nov - Who cited this? | PubMed ID: 17565729 | Fulltext

Molecular heterogeneity in fetal forms of type II lissencephaly.

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Bouchet C, Gonzales M, Vuillaumier-Barrot S, Devisme L, Lebizec C, Alanio E, Bazin A, Bessières-Grattagliano B, Bigi N, Blanchet P, Bonneau D, Bonnières M, Carles D, Delahaye S, Fallet-Bianco C, Figarella-Branger D,

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Human mutation 28(10):1020-7, 2007 Oct - Who cited this? | PubMed ID: 17559086 | Fulltext

Colorectal adenomatous polyposis Associated with MYH mutations: genotype and phenotype characteristics.

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Bouguen G, Manfredi S, Blayau M, Dugast C, Buecher B, Bonneau D, Siproudhis L, David V, and Bretagne JF

Diseases of the colon and rectum 50(10):1612-7, 2007 Oct - Who cited this? | PubMed ID: 17674103 | Fulltext

Endocrine function in a 48,XXYY adult with type 2 diabetes: case report with a review of the literature.

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Dubois S, Illouz F, Pinson L, Bonneau D, Rohmer V, and Guichet A

Annales d'endocrinologie 68(5):384-8, 2007 Oct - Who cited this? | PubMed ID: 17850758 | Fulltext

Molecular and in silico analyses of the full-length isoform of usherin identify new pathogenic alleles in Usher type II patients.

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Baux D, Larrieu L, Blanchet C, Hamel C, Ben Salah S, Vielle A, Gilbert-Dussardier B, Holder M, Calvas P, Philip N, Edery P, Bonneau D, Claustres M, Malcolm S, and Roux AF

Human mutation 28(8):781, 2007 Aug - Who cited this? | PubMed ID: 17405132 | Fulltext

Effects of OPA1 mutations on mitochondrial morphology and apoptosis: relevance to ADOA pathogenesis.

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Olichon A, Landes T, Arnauné-Pelloquin L, Emorine LJ, Mils V, Guichet A, Delettre C, Hamel C, Amati-Bonneau P, Bonneau D, Reynier P, Lenaers G, and Belenguer P

Journal of cellular physiology 211(2):423-30, 2007 May - Who cited this? | PubMed ID: 17167772 | Fulltext

Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease.

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Loiseau D, Chevrollier A, Verny C, Guillet V, Gueguen N, Pou de Crescenzo MA, Ferré M, Malinge MC, Guichet A, Nicolas G, Amati-Bonneau P, Malthièry Y, Bonneau D, and Reynier P

Annals of neurology 61(4):315-23, 2007 Apr - Who cited this? | PubMed ID: 17444508 | Fulltext

New VMD2 gene mutations identified in patients affected by Best vitelliform macular dystrophy.

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Marchant D, Yu K, Bigot K, Roche O, Germain A, Bonneau D, Drouin-Garraud V, Schorderet DF, Munier F, Schmidt D, Le Neindre P, Marsac C, Menasche M, Dufier JL, Fischmeister R, Hartzell C,

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Journal of medical genetics 44(3), 2007 Mar - Who cited this? | PubMed ID: 17287362 | Fulltext

Schimke immunoosseous dysplasia: suggestions of genetic diversity.

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Clewing JM, Fryssira H, Goodman D, Smithson SF, Sloan EA, Lou S, Huang Y, Choi K, Lücke T, Alpay H, André JL, Asakura Y, Biebuyck-Gouge N, Bogdanovic R, Bonneau D, Cancrini C,

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Human mutation 28(3):273, 2007 Mar - Who cited this? | PubMed ID: 17089404 | Fulltext

Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome.

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Stoetzel C, Muller J, Laurier V, Davis EE, Zaghloul NA, Vicaire S, Jacquelin C, Plewniak F, Leitch CC, Sarda P, Hamel C, de Ravel TJ, Lewis RA, Friederich E, Thibault C, Danse JM,

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American journal of human genetics 80(1):1-11, 2007 Jan - Who cited this? | PubMed ID: 17160889 | Fulltext

External and internal geometry of European adults.

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Bertrand S, Skalli W, Delacherie L, Bonneau D, Kalifa G, and Mitton D

Ergonomics 49(15):1547-64, 2006 Dec 15 - Who cited this? | PubMed ID: 17090503 | Fulltext

Pitfalls of homozygosity mapping: an extended consanguineous Bardet-Biedl syndrome family with two mutant genes (BBS2, BBS10), three mutations, but no triallelism.

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Laurier V, Stoetzel C, Muller J, Thibault C, Corbani S, Jalkh N, Salem N, Chouery E, Poch O, Licaire S, Danse JM, Amati-Bonneau P, Bonneau D, Mégarbané A, Mandel JL, and Dollfus H

European journal of human genetics : EJHG 14(11):1195-203, 2006 Nov - Who cited this? | PubMed ID: 16823392 | Fulltext

Refsum's disease may mimic familial Guillain Barre syndrome.

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Verny C, Prundean A, Nicolas G, Pautot V, Maugin D, Levade T, Bonneau D, and Dubas F

Neuromuscular disorders : NMD 16(11):805-8, 2006 Nov - Who cited this? | PubMed ID: 16934464 | Fulltext

[Bardet-Biedl syndrome: a unique family for a major gene (BBS10)].

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Dollfus H, Muller J, Stoetzel C, Laurier V, Bonneau D, Mégarbané A, Poch O, and Mandel JL

Medecine sciences : M/S 22(11):901-4, 2006 Nov - Who cited this? | PubMed ID: 17101080 | Fulltext

BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus.

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Stoetzel C, Laurier V, Davis EE, Muller J, Rix S, Badano JL, Leitch CC, Salem N, Chouery E, Corbani S, Jalk N, Vicaire S, Sarda P, Hamel C, Lacombe D, Holder M,

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Nature genetics 38(5):521-4, 2006 May - Who cited this? | PubMed ID: 16582908 | Fulltext

Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome.

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Niihori T, Aoki Y, Narumi Y, Neri G, Cavé H, Verloes A, Okamoto N, Hennekam RC, Gillessen-Kaesbach G, Wieczorek D, Kavamura MI, Kurosawa K, Ohashi H, Wilson L, Heron D, Bonneau D,

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Nature genetics 38(3):294-6, 2006 Mar - Who cited this? | PubMed ID: 16474404 | Fulltext

USH1A: chronicle of a slow death.

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Gerber S, Bonneau D, Gilbert B, Munnich A, Dufier JL, Rozet JM, and Kaplan J

American journal of human genetics 78(2):357-9, 2006 Feb - Who cited this? | PubMed ID: 16400615 | Fulltext

BBS8 is rarely mutated in a cohort of 128 Bardet-Biedl syndrome families.

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Stoetzel C, Laurier V, Faivre L, Mégarbané A, Perrin-Schmitt F, Verloes A, Bonneau D, Mandel JL, Cossee M, and Dollfus H

Journal of human genetics 51(1):81-4, 2006 - Who cited this? | PubMed ID: 16308660 | Fulltext

Modafinil-induced modulation of working memory and plasma corticosterone in chronically-stressed mice.

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Piérard C, Liscia P, Valleau M, Drouet I, Chauveau F, Huart B, Bonneau D, Jouanin JC, Beaumont M, and Béracochéa D

Pharmacology, biochemistry, and behavior 83(1):1-8, 2006 Jan - Who cited this? | PubMed ID: 16439006 | Fulltext

Eight previously unidentified mutations found in the OA1 ocular albinism gene.

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Mayeur H, Roche O, Vêtu C, Jaliffa C, Marchant D, Dollfus H, Bonneau D, Munier FL, Schorderet DF, Levin AV, Héon E, Sutherland J, Lacombe D, Said E, Mezer E, Kaplan J,

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BMC medical genetics 7:41, 2006 - Who cited this? | PubMed ID: 16646960 | Fulltext

Mitochondrial dynamics and disease, OPA1.

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Olichon A, Guillou E, Delettre C, Landes T, Arnauné-Pelloquin L, Emorine LJ, Mils V, Daloyau M, Hamel C, Amati-Bonneau P, Bonneau D, Reynier P, Lenaers G, and Belenguer P

Biochimica et biophysica acta 1763(5-6):500-9, 2006 - Who cited this? | PubMed ID: 16737747 | Fulltext

OPA1 R445H mutation in optic atrophy associated with sensorineural deafness.

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Amati-Bonneau P, Guichet A, Olichon A, Chevrollier A, Viala F, Miot S, Ayuso C, Odent S, Arrouet C, Verny C, Calmels MN, Simard G, Belenguer P, Wang J, Puel JL, Hamel C,

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Annals of neurology 58(6):958-63, 2005 Dec - Who cited this? | PubMed ID: 16240368 | Fulltext

Tetrahydrobiopterin deficiency exaggerates intimal hyperplasia after vascular injury.

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Wang CH, Li SH, Weisel RD, Fedak PW, Hung A, Li RK, Rao V, Hyland K, Cherng WJ, Errett L, Leclerc Y, Bonneau D, Latter DA, and Verma S

American journal of physiology. Regulatory, integrative and comparative physiology 289(2):R299-304, 2005 Aug - Who cited this? | PubMed ID: 15774769 | Fulltext

Myelinated retinal nerve fibres loss in Leber's hereditary optic neuropathy.

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Gicquel JJ, Salama B, Mercié M, Bonneau D, and Dighiero P

Acta ophthalmologica Scandinavica 83(4):517-8, 2005 Aug - Who cited this? | PubMed ID: 16029287 | Fulltext

Testing for triallelism: analysis of six BBS genes in a Bardet-Biedl syndrome family cohort.

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Hichri H, Stoetzel C, Laurier V, Caron S, Sigaudy S, Sarda P, Hamel C, Martin-Coignard D, Gilles M, Leheup B, Holder M, Kaplan J, Bitoun P, Lacombe D, Verloes A, Bonneau D,

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European journal of human genetics : EJHG 13(5):607, 2005 May - Who cited this? | PubMed ID: 15770229 | Fulltext

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