Europe PMC requires Javascript to function effectively.

Either your web browser doesn't support Javascript or it is currently turned off. In the latter case, please turn on Javascript support in your web browser and reload this page.

Search life-sciences literature (45,103,589 articles, preprints and more)

Suggested authors matching "AUTH:Cordier MP" with an ORCID

Marie-Pierre CORDIER
No affiliation detected
1
Publication
37
Citations
View profile

Search results

1-25 of 102 results

Sort by:

Relevance ^{Relevance: This is determined based on a ranking of criteria including term frequency, rarity of term, recency of article, whether there is a Title or Author field match, etc.}

Times cited

Date

1 2 3 Next ...

Clinical and molecular data in cases of prenatal localized overgrowth disorder: major implication of genetic variants in PI3K-AKT-mTOR signaling pathway.
Bourgon N, Carmignac V, Sorlin A, Duffourd Y, Philippe C, Thauvin-Robinet C, Guibaud L, Faivre L, Vabres P, Kuentz P, Collaborators
Ultrasound Obstet Gynecol, 59(4):532-542, 10 Mar 2022
Cited by: 2 articles | PMID: 34170046
Add to export list
Effects of eight neuropsychiatric copy number variants on human brain structure.
Modenato C, Kumar K, Moreau C, Martin-Brevet S, Huguet G, Schramm C, Jean-Louis M, Martin CO, Younis N, Tamer P, Douard E, Thébault-Dagher F, Côté V, Charlebois AR, Deguire F, Maillard AM, Rodriguez-Herreros B, Pain A, Richetin S, [...] Jacquemont S
Transl Psychiatry, 11(1):399, 20 Jul 2021
Cited by: 13 articles | PMID: 34285187 | PMCID: PMC8292542
Add to export list
This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
Free full text in Europe PMC
Growth charts in Kabuki syndrome 1.
Ruault V, Corsini C, Duflos C, Akouete S, Georgescu V, Abaji M, Alembick Y, Alix E, Amiel J, Amouroux C, Barat-Houari M, Baumann C, Bonnard A, Boursier G, Boute O, Burglen L, Busa T, Cordier MP, Cormier-Daire V, [...] Geneviève D
Am J Med Genet A, 182(3):446-453, 26 Dec 2019
Cited by: 5 articles | PMID: 31876365
Add to export list
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3.
Cameron-Christie SR, Wells CF, Simon M, Wessels M, Tang CZN, Wei W, Takei R, Aarts-Tesselaar C, Sandaradura S, Sillence DO, Cordier MP, Veenstra-Knol HE, Cassina M, Ludwig K, Trevisson E, Bahlo M, Markie DM, Jenkins ZA, Robertson SP
Am J Hum Genet, 105(3):669, 01 Sep 2019
Cited by: 2 articles | PMID: 31491409 | PMCID: PMC6731374
Add to export list Free full text in Europe PMC
Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number Variations.
Cárdenas-de-la-Parra A, Martin-Brevet S, Moreau C, Rodriguez-Herreros B, Fonov VS, Maillard AM, Zürcher NR, 16p11.2 European Consortium, Hadjikhani N, Beckmann JS, Reymond A, Draganski B, Jacquemont S, Collins DL
Neuroimage, 203:116155, 05 Sep 2019
Cited by: 7 articles | PMID: 31494251
Add to export list
Genetic abnormalities in a large cohort of Coffin-Siris syndrome patients.
Sekiguchi F, Tsurusaki Y, Okamoto N, Teik KW, Mizuno S, Suzumura H, Isidor B, Ong WP, Haniffa M, White SM, Matsuo M, Saito K, Phadke S, Kosho T, Yap P, Goyal M, Clarke LA, Sachdev R, McGillivray G, [...] Matsumoto N
J Hum Genet, 64(12):1173-1186, 17 Sep 2019
Cited by: 33 articles | PMID: 31530938
Add to export list
Whole genome paired-end sequencing elucidates functional and phenotypic consequences of balanced chromosomal rearrangement in patients with developmental disorders.
Schluth-Bolard C, Diguet F, Chatron N, Rollat-Farnier PA, Bardel C, Afenjar A, Amblard F, Amiel J, Blesson S, Callier P, Capri Y, Collignon P, Cordier MP, Coubes C, Demeer B, Chaussenot A, Demurger F, Devillard F, Doco-Fenzy M, [...] Sanlaville D
J Med Genet, 56(8):526-535, 28 Mar 2019
Cited by: 25 articles | PMID: 30923172
Add to export list
Exome sequencing in clinical settings: preferences and experiences of parents of children with rare diseases (SEQUAPRE study).
Chassagne A, Pélissier A, Houdayer F, Cretin E, Gautier E, Salvi D, Kidri S, Godard A, Thauvin-Robinet C, Masurel A, Lehalle D, Jean-Marçais N, Thevenon J, Lesca G, Putoux A, Cordier MP, Dupuis-Girod S, Till M, Duffourd Y, [...] Faivre L
Eur J Hum Genet, 27(5):701-710, 01 Feb 2019
Cited by: 17 articles | PMID: 30710147 | PMCID: PMC6461801
Add to export list Free full text in Europe PMC
Wiedemann-Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French cases.
Baer S, Afenjar A, Smol T, Piton A, Gérard B, Alembik Y, Bienvenu T, Boursier G, Boute O, Colson C, Cordier MP, Cormier-Daire V, Delobel B, Doco-Fenzy M, Duban-Bedu B, Fradin M, Geneviève D, Goldenberg A, Grelet M, [...] Morin G
Clin Genet, 94(1):141-152, 17 May 2018
Cited by: 36 articles | PMID: 29574747
Add to export list Review
16p13.11 microduplication in 45 new patients: refined clinical significance and genotype-phenotype correlations.
Allach El Khattabi L, Heide S, Caberg JH, Andrieux J, Doco Fenzy M, Vincent-Delorme C, Callier P, Chantot-Bastaraud S, Afenjar A, Boute-Benejean O, Cordier MP, Faivre L, Francannet C, Gerard M, Goldenberg A, Masurel-Paulet A, Mosca-Boidron AL, Marle N, Moncla A, [...] Pipiras E
J Med Genet, 57(5):301-307, 04 Oct 2018
Cited by: 34 articles | PMID: 30287593
Add to export list
TTC7A mutation must be considered in patients with repeated intestinal atresia associated with early inflammatory bowel disease: Two new case reports and a literature review.
Fayard J, Collardeau S, Bertrand Y, Cordier MP, Malcus C, Dubois R, Mure PY, de Saint Basile G, Louazon T, Rohmer B, Lachaux A, Duclaux R, Peretti N
Arch Pediatr, S0929-693X(18)30112-X, 16 Jun 2018
Cited by: 7 articles | PMID: 29921470
Add to export list
Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study.
Martin-Brevet S, Rodríguez-Herreros B, Nielsen JA, Moreau C, Modenato C, Maillard AM, Pain A, Richetin S, Jønch AE, Qureshi AY, Zürcher NR, Conus P, 16p11.2 European Consortium, Simons Variation in Individuals Project (VIP) Consortium, Chung WK, Sherr EH, Spiro JE, Kherif F, Beckmann JS, [...] Jacquemont S
Biol Psychiatry, 84(4):253-264, 27 Mar 2018
Cited by: 41 articles | PMID: 29778275
Add to export list
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3.
Cameron-Christie SR, Wells CF, Simon M, Wessels M, Tang CZN, Wei W, Takei R, Aarts-Tesselaar C, Sandaradura S, Sillence DO, Cordier MP, Veenstra-Knol HE, Cassina M, Ludwig K, Trevisson E, Bahlo M, Markie DM, Jenkins ZA, Robertson SP
Am J Hum Genet, 102(6):1115-1125, 24 May 2018
Cited by: 15 articles | PMID: 29805041 | PMCID: PMC5992117
Add to export list Free full text in Europe PMC
Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice.
De Tomasi L, David P, Humbert C, Silbermann F, Arrondel C, Tores F, Fouquet S, Desgrange A, Niel O, Bole-Feysot C, Nitschké P, Roume J, Cordier MP, Pietrement C, Isidor B, Khau Van Kien P, Gonzales M, Saint-Frison MH, Martinovic J, [...] Jeanpierre C
Am J Hum Genet, 101(5):803-814, 01 Nov 2017
Cited by: 47 articles | PMID: 29100091 | PMCID: PMC5673669
Add to export list Free full text in Europe PMC
Outcome of isolated agenesis of the corpus callosum: A population-based prospective study.
des Portes V, Rolland A, Velazquez-Dominguez J, Peyric E, Cordier MP, Gaucherand P, Massardier J, Massoud M, Curie A, Pellot AS, Rivier F, Lacalm A, Clément A, Ville D, Guibaud L
Eur J Paediatr Neurol, 22(1):82-92, 05 Sep 2017
Cited by: 19 articles | PMID: 28947381
Add to export list
In utero ultrasound diagnosis of corpus callosum agenesis leading to the identification of orofaciodigital type 1 syndrome in female fetuses.
Alby C, Boutaud L, Bonnière M, Collardeau-Frachon S, Guibaud L, Lopez E, Bruel AL, Aral B, Sonigo P, Roth P, Vibert-Guigue C, Castaigne V, Carbonne B, Joyé N, Faivre L, Cordier MP, Bernabe Gelot A, Clementi M, Mammi I, [...] Attié-Bitach T
Birth Defects Res, 110(4):382-389, 28 Nov 2017
Cited by: 5 articles | PMID: 29193896
Add to export list
Prenatal microarray comparative genomic hybridization: Experience from the two first years of activity at the Lyon university-hospital.
Pons L, Till M, Alix E, Abel C, Boggio D, Bordes A, Caloone J, Raskin FC, Chatron N, Cordier MP, Fichez A, Labalme A, Lajeunesse C, Liaras É, Massoud M, Miribel J, Ollagnon E, Schluth-Bolard C, Vichier-Cerf A, [...] Sanlaville D
J Gynecol Obstet Hum Reprod, 46(3):275-283, 30 Jan 2017
Cited by: 3 articles | PMID: 28403926
Add to export list
Relevance of C5b9 immunostaining in the diagnosis of neonatal hemochromatosis.
Dubruc E, Nadaud B, Ruchelli E, Heissat S, Baruteau J, Broué P, Debray D, Cordier MP, Miossec P, Russo P, Collardeau-Frachon S
Pediatr Res, 81(5):712-721, 13 Jan 2017
Cited by: 7 articles | PMID: 28085791
Add to export list
Antenatal manifestations of inborn errors of metabolism: prenatal imaging findings.
Guibaud L, Collardeau-Frachon S, Lacalm A, Massoud M, Rossi M, Cordier MP, Vianey-Saban C
J Inherit Metab Dis, 40(1):103-112, 16 Nov 2016
Cited by: 3 articles | PMID: 27853988
Add to export list Review
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.
Collardeau-Frachon S, Cordier MP, Rossi M, Guibaud L, Vianey-Saban C
J Inherit Metab Dis, 39(5):597-610, 22 Apr 2016
Cited by: 1 article | PMID: 27106218
Add to export list Review
Otopalatodigital spectrum disorders: refinement of the phenotypic and mutational spectrum.
Moutton S, Fergelot P, Naudion S, Cordier MP, Solé G, Guerineau E, Hubert C, Rooryck C, Vuillaume ML, Houcinat N, Deforges J, Bouron J, Devès S, Le Merrer M, David A, Geneviève D, Giuliano F, Journel H, Megarbane A, [...] Coupry I
J Hum Genet, 61(8):693-699, 19 May 2016
Cited by: 11 articles | PMID: 27193221
Add to export list
Novel NEK8 Mutations Cause Severe Syndromic Renal Cystic Dysplasia through YAP Dysregulation.
Grampa V, Delous M, Zaidan M, Odye G, Thomas S, Elkhartoufi N, Filhol E, Niel O, Silbermann F, Lebreton C, Collardeau-Frachon S, Rouvet I, Alessandri JL, Devisme L, Dieux-Coeslier A, Cordier MP, Capri Y, Khung-Savatovsky S, Sigaudy S, [...] Saunier S
PLoS Genet, 12(3):e1005894, 11 Mar 2016
Cited by: 57 articles | PMID: 26967905 | PMCID: PMC4788435
Add to export list
This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
Free full text in Europe PMC
Fetal phenotypes in otopalatodigital spectrum disorders.
Naudion S, Moutton S, Coupry I, Sole G, Deforges J, Guerineau E, Hubert C, Deves S, Pilliod J, Rooryck C, Abel C, Le Breton F, Collardeau-Frachon S, Cordier MP, Delezoide AL, Goldenberg A, Loget P, Melki J, Odent S, [...] Fergelot P
Clin Genet, 89(3):371-377, 29 Oct 2015
Cited by: 10 articles | PMID: 26404489
Add to export list
[Innovations in diagnosis and treatment about a case of primary failure eruption linked to a PTHR1 gene mutation].
Raberin M, Diesmusch C, Cordier MP, Farges JC
Orthod Fr, 86(3):221-231, 14 Sep 2015
Cited by: 1 article | PMID: 26370593
Add to export list
Radiographic features of the skeleton in disorders of post-squalene cholesterol biosynthesis.
Rossi M, Hall CM, Bouvier R, Collardeau-Frachon S, Le Breton F, Bucourt M, Cordier MP, Vianey-Saban C, Parenti G, Andria G, Le Merrer M, Edery P, Offiah AC
Pediatr Radiol, 45(7):965-976, 03 Feb 2015
Cited by: 11 articles | PMID: 25646736
Add to export list Review

1-25 of 102 results

1 2 3 Next ...

Search life-sciences literature (45,103,589 articles, preprints and more)

Suggested authors matching "AUTH:Cordier MP" with an ORCID Suggested authors have linked their articles in Europe PMC to their ORCID iD. Up to two suggested authors with a matching surname and initial are shown, ordered by the total number of publications they have in Europe PMC.

Search results

Partnerships & funding

Suggested authors matching "AUTH:Cordier MP" with an ORCID