Melanie Eyries

Melanie Eyries

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Melanie Eyries

Melanie Eyries

Publications by authors named "Melanie Eyries"

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Soft tissue angiomatosis: another PIK3CA-related disorder.

Histopathology 2019 Oct 20. Epub 2019 Oct 20.

Department of Pathology, Hôpital Universitaire Necker-Enfants Malades, APHP, Paris, France.

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http://dx.doi.org/10.1111/his.14021DOI Listing
October 2019

mutation causing pulmonary arterial hypertension and lung disease.

Eur Respir J 2019 Aug 22;54(2). Epub 2019 Aug 22.

Pôle des spécialités médicales/département de pneumologie, CHRU de Nancy, Vandœuvre-lès-Nancy, France

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http://dx.doi.org/10.1183/13993003.00388-2019DOI Listing
August 2019

Clinical implications of CTNNA1 germline mutations in asymptomatic carriers.

Gastric Cancer 2019 07 4;22(4):899-903. Epub 2018 Dec 4.

Laboratoire d'Oncogénétique, Unité fonctionnelle d'Oncogénétique, Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière AP-HP, 75013, Paris, France.

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http://link.springer.com/10.1007/s10120-018-00907-7
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http://dx.doi.org/10.1007/s10120-018-00907-7DOI Listing
July 2019

Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis.

Authors:
Christopher J Rhodes Ken Batai Marta Bleda Matthias Haimel Laura Southgate Marine Germain Michael W Pauciulo Charaka Hadinnapola Jurjan Aman Barbara Girerd Amit Arora Jo Knight Ken B Hanscombe Jason H Karnes Marika Kaakinen Henning Gall Anna Ulrich Lars Harbaum Inês Cebola Jorge Ferrer Katie Lutz Emilia M Swietlik Ferhaan Ahmad Philippe Amouyel Stephen L Archer Rahul Argula Eric D Austin David Badesch Sahil Bakshi Christopher Barnett Raymond Benza Nitin Bhatt Harm J Bogaard Charles D Burger Murali Chakinala Colin Church John G Coghlan Robin Condliffe Paul A Corris Cesare Danesino Stéphanie Debette C Gregory Elliott Jean Elwing Melanie Eyries Terry Fortin Andre Franke Robert P Frantz Adaani Frost Joe G N Garcia Stefano Ghio Hossein-Ardeschir Ghofrani J Simon R Gibbs John Harley Hua He Nicholas S Hill Russel Hirsch Arjan C Houweling Luke S Howard Dunbar Ivy David G Kiely James Klinger Gabor Kovacs Tim Lahm Matthias Laudes Rajiv D Machado Robert V MacKenzie Ross Keith Marsolo Lisa J Martin Shahin Moledina David Montani Steven D Nathan Michael Newnham Andrea Olschewski Horst Olschewski Ronald J Oudiz Willem H Ouwehand Andrew J Peacock Joanna Pepke-Zaba Zia Rehman Ivan Robbins Dan M Roden Erika B Rosenzweig Ghulam Saydain Laura Scelsi Robert Schilz Werner Seeger Christian M Shaffer Robert W Simms Marc Simon Olivier Sitbon Jay Suntharalingam Haiyang Tang Alexander Y Tchourbanov Thenappan Thenappan Fernando Torres Mark R Toshner Carmen M Treacy Anton Vonk Noordegraaf Quinten Waisfisz Anna K Walsworth Robert E Walter John Wharton R James White Jeffrey Wilt Stephen J Wort Delphine Yung Allan Lawrie Marc Humbert Florent Soubrier David-Alexandre Trégouët Inga Prokopenko Richard Kittles Stefan Gräf William C Nichols Richard C Trembath Ankit A Desai Nicholas W Morrell Martin R Wilkins

Lancet Respir Med 2019 Mar 5;7(3):227-238. Epub 2018 Dec 5.

Department of Medicine, Imperial College London, London, UK. Electronic address:

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http://dx.doi.org/10.1016/S2213-2600(18)30409-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391516PMC
March 2019

Prenatal molecular diagnosis in RASA1-related disease.

Prenat Diagn 2017 12 21;37(12):1261-1264. Epub 2017 Nov 21.

Service de Génétique, Hôpital Ambroise Paré, Assistance Publique Hôpitaux de Paris, Boulogne-Billancourt, France.

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http://dx.doi.org/10.1002/pd.5165DOI Listing
December 2017

Clinical and genetic findings in children with central nervous system arteriovenous fistulas.

Ann Neurol 2017 Dec 12;82(6):972-980. Epub 2017 Dec 12.

Department of genetics, Hopital Pitié-Salpêtrière, Paris, France.

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http://dx.doi.org/10.1002/ana.25106DOI Listing
December 2017

Clinical phenotypes and outcomes of heritable and sporadic pulmonary veno-occlusive disease: a population-based study.

Lancet Respir Med 2017 02 11;5(2):125-134. Epub 2017 Jan 11.

University Paris-Sud, Faculté de Médecine, Paris, F-94270, France; AP-HP, Centre de Référence de l'Hypertension Pulmonaire Sévère, Département Hospitalo-Universitaire (DHU) Thorax Innovation (TORINO), Service de Pneumologie, Hôpital de Bicêtre, Le Kremlin Bicêtre, Paris, France; UMR_S 999, Univ. Paris-Sud, INSERM, Laboratoire d'Excellence (LabEx) en Recherche sur le Médicament et l'Innovation Thérapeutique (LERMIT), Centre Chirurgical Marie Lannelongue, Le Plessis Robinson, Paris, France. Electronic address:

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http://dx.doi.org/10.1016/S2213-2600(16)30438-6DOI Listing
February 2017

Molecular Genetic Diagnosis of Pulmonary Arterial Hypertension: An Increased Complexity.

Rev Esp Cardiol (Engl Ed) 2016 Nov 12;69(11):1003-1004. Epub 2016 Sep 12.

Department of Genetics, GH Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris; UMR_S 1166, Université Paris-Sorbonne UPMC, and INSERM, Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.rec.2016.05.026DOI Listing
November 2016

Genetic analyses in a cohort of children with pulmonary hypertension.

Eur Respir J 2016 10 1;48(4):1118-1126. Epub 2016 Sep 1.

Genetics Dept, GH Pitié-Salpêtrière, Assistance Publique Hôpitaux de Paris, Paris, France Sorbonne Universités, UPMC Univ Paris 06, INSERM, UMR_S 1166-ICAN, Paris, France ICAN Institute for Cardiometabolism and Nutrition, Paris, France.

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http://dx.doi.org/10.1183/13993003.00211-2016DOI Listing
October 2016

Genetic counselling in a national referral centre for pulmonary hypertension.

Eur Respir J 2016 Feb 23;47(2):541-52. Epub 2015 Dec 23.

Université Paris Sud, Faculté de Médecine, Université Paris-Saclay, Le Kremlin Bicêtre, France AP-HP, Centre de Référence de l'Hypertension Pulmonaire Sévère, Département Hospitalo-Universitaire (DHU) Thorax Innovation (TORINO), Service de Pneumologie, Hôpital de Bicêtre, Le Kremlin Bicêtre, France UMR_S999, Université Paris-Sud, INSERM, Laboratoire d'Excellence (LabEx) en Recherche sur le Médicament et l'Innovation Thérapeutique (LERMIT), Centre Chirurgical Marie Lannelongue, Le Plessis Robinson, France

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http://erj.ersjournals.com/content/erj/early/2015/12/22/1399
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http://erj.ersjournals.com/lookup/doi/10.1183/13993003.00717
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http://dx.doi.org/10.1183/13993003.00717-2015DOI Listing
February 2016

Characteristics of pulmonary arterial hypertension in affected carriers of a mutation located in the cytoplasmic tail of bone morphogenetic protein receptor type 2.

Chest 2015 May;147(5):1385-1394

University Paris-Sud, Le Kremlin-Bicêtre, France; Assistance Publique-Hôpitaux de Paris (AP-HP), Service de Pneumologie, Centre de Référence de l'Hypertension Pulmonaire Sévère, DHU Thorax Innovation, Hôpital Bicêtre, Le Kremlin-Bicêtre, France; Institut National de la Santé et de la Recherche Médicale (INSERM) U999, LabEx LERMIT, Centre Chirurgical Marie Lannelongue, Le Plessis Robinson, France. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00123692153836
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http://dx.doi.org/10.1378/chest.14-0880DOI Listing
May 2015

Mechanisms of exertional dyspnoea in pulmonary veno-occlusive disease with EIF2AK4 mutations.

Eur Respir J 2014 Oct 19;44(4):1069-72. Epub 2014 Aug 19.

AP-HP, Hôpital Universitaire de Bicêtre, Service d'Explorations Fonctionnelles Respiratoires, Centre de Référence de l'Hypertension Pulmonaire Sévère, DHU TORINO "Thorax Innovation", Le Kremlin-Bicêtre, France Univ. Paris-Sud 11, Faculté de médecine, Le Kremlin-Bicêtre, France INSERM U999, LabEx LERMIT, Centre Chirurgical Marie Lannelongue, Le Plessis-Robinson, France

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http://dx.doi.org/10.1183/09031936.00088914DOI Listing
October 2014

EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension.

Nat Genet 2014 Jan 1;46(1):65-9. Epub 2013 Dec 1.

1] Unité Mixte de Recherche en Santé (UMR_S 956), Université Pierre and Marie Curie Université Paris 06 (UPMC) and Institut National de la Santé et de la Recherche Médicale (INSERM), Paris, France. [2] Genetics Department, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France. [3] Institute for Cardiometabolism and Nutrition (ICAN), Paris, France.

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http://dx.doi.org/10.1038/ng.2844DOI Listing
January 2014

Bone morphogenetic proteins protect pulmonary microvascular endothelial cells from apoptosis by upregulating α-B-crystallin.

Arterioscler Thromb Vasc Biol 2013 Nov 26;33(11):2577-84. Epub 2013 Sep 26.

From the UMR_S 956; Univ Paris 06 (UPMC); Institut National de la Santé et de la Recherche Médicale (INSERM), F-75013, Paris (M.C., M.E., O.P., S.M., F.D., K.M., S.N., F.S.); ICAN Institute for Cardiometabolism and Nutrition, Paris, France (M.E., O.P., S.M., F.D., S.N., F.S.); and UMR_S 999; INSERM; Univ Paris-Sud; LabEx LERMIT, Centre Chirurgical Marie Lannelongue, Le Plessis Robinson, France (N.G.).

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http://dx.doi.org/10.1161/ATVBAHA.113.301976DOI Listing
November 2013

Clinical and genetic characteristics of Chinese patients with hereditary haemorrhagic telangiectasia-associated pulmonary hypertension.

Eur J Clin Invest 2013 Oct 6;43(10):1016-24. Epub 2013 Aug 6.

Department of Cardiology, the 4th Affiliated Hospital, Harbin Medical University, Harbin, China.

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http://dx.doi.org/10.1111/eci.12138DOI Listing
October 2013

A novel channelopathy in pulmonary arterial hypertension.

N Engl J Med 2013 Jul;369(4):351-361

Departments of Pediatrics (L.M., E.B.R., W.K.C.), Pharmacology (D.R.-C., K.S.S., R.S.K.), and Pathology (A.B.), Columbia University Medical Center, New York; the Departments of Pediatrics (E.D.A.) and Medicine (J.E.L.), Vanderbilt University Medical Center, Nashville; the Genetics Department, Hospital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris (APHP), Institut National de la Santé et de la Recherche Médicale (INSERM), and Université Pierre et Marie Curie (UPMC) Unité Mixte de Recherche en Santé (UMRS) 956, Institute of Cardiometabolism and Nutrition (ICAN) (M.E., F.S.); and INSERM-UPMC UMRS 937, ICAN (M.G., D.-A.T.) - all in Paris; and APHP, Département Hospitalo-Universitaire Thorax Innovation (DHU TORINO), Service de Pneumologie, Hôpital Bicêtre; Université Paris-Sud, Laboratoire d'Excellence en Recherche sur le Médicament et Innovation Thérapeutique (LERMIT); and INSERM UMRS 999 - all in Le Kremlin-Bicêtre, France (B.G., D.M., M.H.).

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http://dx.doi.org/10.1056/NEJMoa1211097DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3792227PMC
July 2013

Somatic mosaicism and double somatic hits can lead to MSI colorectal tumors.

Fam Cancer 2013 Mar;12(1):27-33

Department of Digestive Surgery, Hôpital Saint Antoine (AP-HP), Paris VI University, Paris, France.

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http://dx.doi.org/10.1007/s10689-012-9568-9DOI Listing
March 2013

Inhibition of apelin expression by BMP signaling in endothelial cells.

Am J Physiol Cell Physiol 2012 Dec 15;303(11):C1139-45. Epub 2012 Aug 15.

UMR_S 956 INSERM, 91 bvd de l'hôpital, F-75634 Paris cedex 13, France.

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http://www.physiology.org/doi/10.1152/ajpcell.00168.2012
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http://dx.doi.org/10.1152/ajpcell.00168.2012DOI Listing
December 2012

Hypoxia-induced apelin expression regulates endothelial cell proliferation and regenerative angiogenesis.

Circ Res 2008 Aug 10;103(4):432-40. Epub 2008 Jul 10.

INSERM UMRS 525, Université Pierre et Marie Curie, Paris, France.

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http://dx.doi.org/10.1161/CIRCRESAHA.108.179333DOI Listing
August 2008

Inducible platelet-derived growth factor D-chain expression by angiotensin II and hydrogen peroxide involves transcriptional regulation by Ets-1 and Sp1.

Blood 2006 Mar 27;107(6):2322-9. Epub 2005 Sep 27.

Centre for Vascular Research, Department of Pathology, University of New South Wales, Sydney NSW 2052 Australia.

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http://dx.doi.org/10.1182/blood-2005-06-2377DOI Listing
March 2006

Modulation of growth factor gene expression in vascular cells by oxidative stress.

Endothelium 2004 Mar-Apr;11(2):133-9

The Centre for Vascular Research, Department of Pathology, The University of New South Wales, Sydney, Australia.

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http://dx.doi.org/10.1080/10623320490482691DOI Listing
October 2004

Phorbol ester induction of angiotensin-converting enzyme transcription is mediated by Egr-1 and AP-1 in human endothelial cells via ERK1/2 pathway.

Circ Res 2002 Nov;91(10):899-906

Institut National de la Santé et de la Recherche Médicale, Unit 525, Faculté de Médecine Pitié-Sapétrière, Paris, France.

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http://dx.doi.org/10.1161/01.res.0000042703.39845.b4DOI Listing
November 2002