About: Nabila Bouatia-Naji

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

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) chercheuse (fr) investigadora (es) ഗവേഷക (ml) wetenschapper (nl) дослідниця (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) researcher (en-ca) researcher (en-gb) researcher (en-us) hulumtuese (sq) ricercatrice (it) investigadora (ca) investigadora (gl) investigadora (pt) investigadora (ast)
rdfs:label	Nabila Bouatia-Naji (en) Nabila Bouatia-Naji (es) Nabila Bouatia-Naji (fr) Nabila Bouatia-Naji (it) Nabila Bouatia-Naji (nl) Nabila Bouatia-Naji (sl) Nabila Bouatia-Naji (ast)
skos:prefLabel	Nabila Bouatia-Naji (en) Nabila Bouatia-Naji (es) Nabila Bouatia-Naji (fr) Nabila Bouatia-Naji (it) Nabila Bouatia-Naji (nl) Nabila Bouatia-Naji (sl) Nabila Bouatia-Naji (ast)
name	Nabila Bouatia-Naji (en) Nabila Bouatia-Naji (es) Nabila Bouatia-Naji (fr) Nabila Bouatia-Naji (it) Nabila Bouatia-Naji (nl) Nabila Bouatia-Naji (sl) Nabila Bouatia-Naji (ast)
given name	wds:Q30225478-F027F7C9-3034-40CC-ADF2-4B4ADA22683E
given name	Nabila
instance of	wds:Q30225478-604793F5-C072-400A-B402-8A062506FD92
instance of	Homo sapiens
award received	wds:Q30225478-09a31a2c-4e95-4e8c-d538-7d56cd820c71
award received	Fellow of the African Academy of Sciences
doctoral advisor	wds:Q30225478-F82B8D3A-C7F4-412B-9BC7-50F8B56E9827
doctoral student	wds:Q30225478-40814722-F9A8-4B15-9097-9795AE239AE7
doctoral advisor	Philippe Froguel
doctoral student	Mengyao Yu
occupation	wds:Q30225478-33EE4CE2-13A7-46ED-BBDA-6687D4CCF2ED
employer	wds:Q30225478-68474176-8FF1-49DE-A39D-7DA8C7C609E8 wds:Q30225478-A05E72B7-6F19-4B6D-8A03-49C91188A05E wds:Q30225478-A2C3CFB7-EDC9-440F-B0F8-A0F71762D39C
sex or gender	wds:Q30225478-68E138FC-FA2E-477E-AB79-0D32E8B12441
ISNI	wds:Q30225478-D85ADC45-86AE-43AF-B6EB-6128E4F4C38F
VIAF ID	wds:Q30225478-70829484-6F93-43E8-8BFB-7E43F89738BF
IdRef ID	wds:Q30225478-AFD4C925-2FF1-4F55-AC13-1DFB83FCDC43
date of birth	wds:Q30225478-7B540DDE-D1D9-4E82-8E33-CDBE12F34FD6
VIAF ID	http://viaf.org/viaf/198851534
IdRef ID	http://www.idref.fr/112489354/id
occupation	researcher
employer	Paris Descartes University French National Institute of Health and Medical Research
sex or gender	female organism
ISNI	0000000140848522
VIAF ID	198851534
IdRef ID	112489354
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
Springer Nature person ID	wds:Q30225478-71BA8E12-9E3E-44AF-BE7C-9CD68775AF76
ORCID iD	wds:Q30225478-3497F550-EFED-40BC-B617-3E7675697A51
Dimensions author ID	wds:Q30225478-E0892E0E-EED3-42AE-A578-4188F50AF55E
ORCID iD	https://orcid.org/0000-0001-5424-2134
Springer Nature person ID	0626061227.06
ORCID iD	0000-0001-5424-2134
Dimensions author ID	0626061227.06
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q30225478
is author of	Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes ACDC/Adiponectin Polymorphisms Are Associated With Severe Childhood and Adult Obesity Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution Genome-wide association analyses identify 18 new loci associated with serum urate concentrations Exome sequencing in seven families and gene-based association studies indicate genetic heterogeneity and suggest possible candidates for fibromuscular dysplasia. A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk G-allele of intronic rs10830963 in MTNR1B confers increased risk of impaired fasting glycemia and type 2 diabetes through an impaired glucose-stimulated insulin release: studies involving 19,605 Europeans Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways Genome-wide association study identifies five loci associated with lung function Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes A genome-wide association search for type 2 diabetes genes in African Americans

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