Paul Laissue

Citado por

	Total	Desde 2019
Citas	3539	1446
Índice h	31	21
Índice i10	65	40

420

210

105

315

20042005200620072008200920102011201220132014201520162017201820192020202120222023202417 31 37 58 109 93 113 132 144 137 143 186 177 228 404 212 345 284 284 241 77

Acceso público

Ver todo

12 artículos

3 artículos

disponibles

no disponibles

Basado en requisitos de financiación

Coautores

Vaiman DanielDepartment Genetics and Development, Cochin Institute, ParisDirección de correo verificada de inserm.fr
VEITIA Reiner A.Professor, Université de Paris. Head François Jacob Institute, CEA. Editor In Chief Clinical GenetDirección de correo verificada de ijm.fr
Patino Liliana C.Mucosal Immunology Section, National Institute of Dental and Craniofacial Research (NIDCR), NationalDirección de correo verificada de nih.gov
Oscar Ortega-RecaldeUniversidad Nacional de Colombia | University of OtagoDirección de correo verificada de unal.edu.co
SAAD ALIPROFESSEUR D'HISTOLOGIE-EMBRYOLOGIE ET DE GENETIQUEDirección de correo verificada de rns.tn
Diego A. OjedaUniversity of MiamiDirección de correo verificada de miami.edu
Gaetan BurgioGroup Leader, The Australian National UniversityDirección de correo verificada de anu.edu.au
Diego Forero, MD, PhDResearcher, School of Health and Sport Sciences, Fundación Universitaria del Área AndinaDirección de correo verificada de areandina.edu.co
Ivo GutDirector, Centro Nacional de Analisis Genomico, CNAG-CRG, Center for Genomic RegulationDirección de correo verificada de cnag.crg.eu
Sandrine CaburetUniversité Paris DiderotDirección de correo verificada de ijm.fr
Bérénice A. BenayounAssistant Professor, USC Davis School of GerontologyDirección de correo verificada de usc.edu
jeyabalan nallathambiScentistDirección de correo verificada de narayananethralaya.com
Adrián LLerena MD PhD Professor Cli...INUBE Biosanitary University Research Institute. University of Extremadura. CICAB Clinical ResearchDirección de correo verificada de unex.es
Sonia R GroverDirector, Dept Gynaecology Royal Children's Hospital; Uni MelbourneDirección de correo verificada de rch.org.au
Erin TurbittUniversity of Technology SydneyDirección de correo verificada de uts.edu.au
Peter KoopmanThe University of QueenslandDirección de correo verificada de imb.uq.edu.au
Giovanni LeviResearch Director, UMR7221 CNRS/MNHN ParisDirección de correo verificada de mnhn.fr
Stefan WhiteWhiteFox Science ConsultingDirección de correo verificada de whitefoxsc.com
Krishnaswamy SRetd from Madurai Kamaraj
Carlos Fernando Prada QuirogaProfesor de Genética y Evolucion, Universidad del Tolima. Ibaguè, ColombiaDirección de correo verificada de ut.edu.co

Seguir

Paul Laissue

LATAM Medical Director. Orphan Diseases Unit. Biopas Laboratoires. BIOPAS Group. Inserm U1016, CNRS

Dirección de correo verificada de biopasgroup.com

Human Genetics Genomics Quantitative Genetics Complex Diseases


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
Undertreatment strongly decreases prognosis of breast cancer in elderly women C Bouchardy, E Rapiti, G Fioretta, P Laissue, I Neyroud-Caspar, ... Journal of clinical oncology 21 (19), 3580-3587, 2003	630	2003
Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure P Laissue, S Christin-Maitre, P Touraine, F Kuttenn, O Ritvos, K Aittomaki, ... European Journal of Endocrinology 154 (5), 739-744, 2006	345	2006
Expressional and Epigenetic Alterations of Placental Serine Protease Inhibitors: SERPINA3 Is a Potential Marker of Preeclampsia ST Chelbi, F Mondon, H Jammes, C Buffat, TM Mignot, J Tost, F Busato, ... Hypertension 49 (1), 76-83, 2007	168	2007
The forkhead-box family of transcription factors: key molecular players in colorectal cancer pathogenesis P Laissue Molecular cancer 18 (1), 5, 2019	121	2019
Recent advances in the study of genes involved in non-syndromic premature ovarian failure P Laissue, G Vinci, RA Veitia, M Fellous Molecular and Cellular Endocrinology 282 (1-2), 101-111, 2008	104	2008
Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis CP Diggle, DA Parry, CV Logan, P Laissue, C Rivera, CM Restrepo, ... Human mutation 33 (8), 1175-1181, 2012	101	2012
Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2 P Laissue, B Lakhal, BA Benayoun, A Dipietromaria, R Braham, ... Journal of medical genetics 46 (7), 455-457, 2009	87	2009
Novel genes and mutations in patients affected by recurrent pregnancy loss P Quintero-Ronderos, E Mercier, M Fukuda, R González, CF Suárez, ... PloS one 12 (10), e0186149, 2017	80	2017
New mutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing LC Patiño, I Beau, C Carlosama, JC Buitrago, R González, CF Suárez, ... Human reproduction 32 (7), 1512-1520, 2017	80	2017
Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations DJ Fonseca, LC Patiño, YC Suárez, A de Jesús Rodríguez, HE Mateus, ... Fertility and sterility 104 (1), 154-162. e2, 2015	78	2015
A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiency C Carlosama, M Elzaiat, LC Patiño, HE Mateus, RA Veitia, P Laissue Human molecular genetics 26 (16), 3161-3166, 2017	74	2017
ATG7 and ATG9A loss-of-function variants trigger autophagy impairment and ovarian failure C Delcour, L Amazit, LC Patino, F Magnin, J Fagart, B Delemer, J Young, ... Genetics in Medicine 21 (4), 930-938, 2019	72	2019
Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing P Laissue Molecular and cellular endocrinology 411, 243-257, 2015	72	2015
BMP15 mutations associated with primary ovarian insufficiency reduce expression, activity, or synergy with GDF9 LC Patiño, KL Walton, TD Mueller, KE Johnson, W Stocker, D Richani, ... The Journal of Clinical Endocrinology & Metabolism 102 (3), 1009-1019, 2017	64	2017
Success stories in genomic medicine from resource-limited countries K Mitropoulos, H Al Jaibeji, DA Forero, P Laissue, A Wonkam, ... Human genomics 9, 1-7, 2015	63	2015
Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia A Ducat, L Doridot, R Calicchio, C Méhats, JL Vilotte, J Castille, ... Scientific reports 6 (1), 19196, 2016	61	2016
Identification of 34 novel and 56 known FOXL2 mutations in patients with blepharophimosis syndrome D Beysen, S De Jaegere, D Amor, P Bouchard, S Christin‐Maitre, ... Human mutation 29 (11), E205-E219, 2008	59	2008
Centimorgan-range one-step mapping of fertility traits using interspecific recombinant congenic mice D L'Hôte, C Serres, P Laissue, A Oulmouden, C Rogel-Gaillard, ... Genetics 176 (3), 1907-1921, 2007	56	2007
Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial premature ovarian failure S Caburet, P Zavadakova, Z Ben-Neriah, K Bouhali, A Dipietromaria, ... PLoS one 7 (3), e33412, 2012	52	2012
Biallelic HERC1 mutations in a syndromic form of overgrowth and intellectual disability O Ortega‐Recalde, OI Beltrán, JM Gálvez, A Palma‐Montero, ... Clinical genetics 88 (4), e1-e3, 2015	50	2015

El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.

Artículos 1–20

Citas por año

Citas duplicadas

Citas combinadas

Añadir coautoresCoautores

Seguir

Citado por

Coautores