About: Nicolas Richard

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About: Nicolas Richard Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher (ORCID 0000-0003-0702-7399)

Attributes	Values
rdf:type	Item
description	forskare (sv) 연구원 (ko) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) հետազոտող (hy) researcher (ORCID 0000-0003-0702-7399) (en)
rdfs:label	Nicolas Richard (en) Nicolas Richard (es) Nicolas Richard (nl) Nicolas Richard (ast)
skos:prefLabel	Nicolas Richard (en) Nicolas Richard (es) Nicolas Richard (nl) Nicolas Richard (ast)
name	Nicolas Richard (en) Nicolas Richard (es) Nicolas Richard (nl) Nicolas Richard (ast)
Scopus author ID	wds:Q57419747-6FEDAD8B-0090-411C-AFA4-A17C119EFA8D
Scopus author ID	16231189800
given name	wds:Q57419747-D4D5E53E-6E95-437E-B803-3949FA0E359C
given name	Nicolas
instance of	wds:Q57419747-CCEFE2C1-F534-42C3-9234-E699ED33E90B
instance of	Homo sapiens
occupation	wds:Q57419747-CC7A6E7E-DCC6-48C9-A9B4-6CA6AD50F858
employer	wds:Q57419747-66F752DD-92FF-4E70-930A-5074C70162E4
sex or gender	wds:Q57419747-100D7C17-E86A-49BC-AAD2-D954C43B7029
VIAF ID	wds:Q57419747-513E14A2-CB02-44AB-AD12-9526C2557323
IdRef ID	wds:Q57419747-27B0B747-D540-48D2-BAAB-389E1D9D45EF
family name	wds:Q57419747-8813F7A7-42B5-4BD1-9105-E3328A38E353
VIAF ID	http://viaf.org/viaf/308790122
IdRef ID	http://www.idref.fr/178137480/id
occupation	researcher
employer	CHU Côte de Nacre
sex or gender	male
VIAF ID	308790122
IdRef ID	178137480
family name	Richard
ORCID iD	wds:Q57419747-BC9ACBAD-8D5B-479C-8CC9-DD753B13C75A
ORCID iD	https://orcid.org/0000-0003-0702-7399
ORCID iD	0000-0003-0702-7399
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57419747
is author of	Loss of methylation at GNAS exon A/B is associated with increased intrauterine growth Paternal GNAS mutations lead to severe intrauterine growth retardation (IUGR) and provide evidence for a role of XLαs in fetal development. A multicenter blinded study evaluating EGFR and KRAS mutation testing methods in the clinical non-small cell lung cancer setting--IFCT/ERMETIC2 Project Part 1: Comparison of testing methods in 20 French molecular genetic National Cancer Institute pl Expected benefits of topotecan combined with lapatinib in recurrent ovarian cancer according to biological profile: a phase 2 trial The expression of aromatase in gonadotropes is regulated by estradiol and gonadotropin-releasing hormone in a manner that differs from the regulation of luteinizing hormone. Cross-Validation Study for Epidermal Growth Factor Receptor and KRAS Mutation Detection in 74 Blinded Non-small Cell Lung Carcinoma Samples: A Total of 5550 Exons Sequenced by 15 Molecular French Laboratories (Evaluation of the EGFR Mutation Status f Progressive osseous heteroplasia: a model for the imprinting effects of GNAS inactivating mutations in humans An apoptosis methylation prognostic signature for early lung cancer in the IFCT-0002 trial. De novo 15q13.3 microdeletion with cryptogenic West syndrome A new FSHbeta mutation in a 29-year-old woman with primary amenorrhea and isolated FSH deficiency: functional characterization and ovarian response to human recombinant FSH. Array CGH analysis in high-risk pregnancies: comparing DNA from cultured cells and cell-free fetal DNA Vitamin D-Dependent Rickets Type 1B (25-Hydroxylase Deficiency): A Rare Condition or a Misdiagnosed Condition? Routine molecular profiling of patients with advanced non-small-cell lung cancer: results of a 1-year nationwide programme of the French Cooperative Thoracic Intergroup (IFCT). CYP24A1 Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive Trait. Diagnosis and management of congenital hypothyroidism associated with pseudohypoparathyroidism Identification of I1171N resistance mutation in ALK-positive non-small-cell lung cancer tumor sample and circulating tumor DNA. Cost-effectiveness of three strategies for second-line erlotinib initiation in nonsmall-cell lung cancer: the ERMETIC study part 3. Maternal Transmission Ratio Distortion of GNAS Loss-of-Function Mutations Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders Molecular characterization of a recurrent 10.9 kb CYP24A1 deletion in Idiopathic Infantile Hypercalcemia [Epigenetics and pseudohypoparathyroidism] Seasonal expression of KiSS-1 and the pituitary gonadotropins LHβ and FSHβ in adult male Libyan jird (Meriones libycus). Identification by array-Comparative Genomic Hybridization (array-CGH) of a large deletion of luteinizing hormone receptor gene combined with a missense mutation in a patient diagnosed with a 46,XY disorder of sex development and application to prena High frequency of paternal iso or heterodisomy at chromosome 20 associated with sporadic pseudohypoparathyroidism 1B Relevance of Detection of Mechanisms of Resistance to ALK Inhibitors in ALK-Rearranged NSCLC in Routine Practice FSHbeta gene mutation in a female with delayed puberty and hypogonadism: response to recombinant human FSH. [New biological treatments for lung cancer] Clinical Relevance of EGFR- or KRAS-mutated Subclones in Patients With Advanced Non-small-cell Lung Cancer Receiving Erlotinib in a French Prospective Cohort (IFCT ERMETIC2 Cohort - Part 2)
is author of	wds:Q33403609-9A492E30-18D0-47F0-9DFB-70C45C0239B7 wds:Q35442006-16B13D04-BA0F-407A-A5A9-DE10BFAAC7D0 wds:Q38761734-4FCDF3BF-90F1-4758-85A7-D4037F420DC4 wds:Q86538571-F144170F-D765-43A9-B164-2A5C7727EAE7 wds:Q87225692-E953CD09-44B4-46D1-9BA9-4ABA86114E7C wds:Q92319000-C526E4A8-59E0-4AFB-A386-35920670D985 wds:Q57419586-4B18CEC9-C6F7-4137-B167-1E86C2129F60 wds:Q64042734-F7286E36-0617-4F72-9BDA-3B42ECFD8A85 wds:Q84958201-52941666-6ADE-460F-8234-613691C19D8C wds:Q38916815-F6B0B0EC-9799-451E-8477-A6CCE3E04AA1 wds:Q40096915-7E67FDAA-5C50-49B6-BCA7-2E781E3DB2F1 wds:Q54587266-00111013-499F-401F-8380-F36F5971CEB4 wds:Q51548102-EC0ED917-3AFB-439C-9F03-D7716CB93905 wds:Q64039725-97700001-B893-4273-8430-27708C1B0E38 wds:Q92416792-40BE97F9-4183-4E28-AA31-414804EA4A94 wds:Q90730812-0AA3D8B6-FA1D-46AE-833C-BCEF5D394859 wds:Q33928609-676AB281-77C0-4B5D-B62B-9914BF15FF3E wds:Q40269757-00F7C892-0B73-48E3-80A9-FD47492AF0E5 wds:Q43196277-59A03508-4208-4626-80EB-C31292F808D0 wds:Q39067796-C122DDC2-B0BC-4CF0-B3BE-60C4692D07A8 wds:Q50585675-BA43EFCD-B443-46FF-AE11-8FE1A1D47239 wds:Q80212282-B8C0EF85-CBDF-4383-BAB1-1CD4AE438F7C wds:Q91208912-0A2E8946-B954-4699-98B0-DCC2BB1880A5 wds:Q37149603-0673A185-6B46-455C-B4D7-0C9B604C0353 wds:Q39766338-BD13CEAC-59EC-4DD5-B32E-7B9530B28ED5 wds:Q28280832-F41F3EB7-6200-496F-9D08-6F8F1B4473A8

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