About: Taneli Raivio

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

Finnish researcher, professor of translational pediatrics at the University of Helsinki

Attributes	Values
rdf:type	Item
description	Fins hoogleraar (nl) finnischer Professor (de) Finnish researcher, professor of translational pediatrics at the University of Helsinki (en) suomalainen tutkija, Helsingin yliopiston translationaalisen lastentautiopin professori (fi)
rdfs:label	Taneli Raivio (ca) Taneli Raivio (en) Taneli Raivio (es) Taneli Raivio (fi) Taneli Raivio (fr) Taneli Raivio (ga) Taneli Raivio (it) Taneli Raivio (nl) Taneli Raivio (sl) Taneli Raivio (sq) Taneli Raivio (ast)
skos:prefLabel	Taneli Raivio (ca) Taneli Raivio (en) Taneli Raivio (es) Taneli Raivio (fi) Taneli Raivio (fr) Taneli Raivio (ga) Taneli Raivio (it) Taneli Raivio (nl) Taneli Raivio (sl) Taneli Raivio (sq) Taneli Raivio (ast)
name	Taneli Raivio (ca) Taneli Raivio (en) Taneli Raivio (es) Taneli Raivio (fi) Taneli Raivio (fr) Taneli Raivio (ga) Taneli Raivio (it) Taneli Raivio (nl) Taneli Raivio (sl) Taneli Raivio (sq) Taneli Raivio (ast)
given name	wds:Q30347924-98A1668B-8498-4D11-8B4A-D520EE6E3FBC
given name	Taneli
instance of	wds:Q30347924-ABE01B85-5961-4522-8308-C4CC2E55055D
instance of	Homo sapiens
employer	wds:Q30347924-448F86C7-C7E1-43EB-84EE-AFDBF94CEA1E
place of birth	wds:Q30347924-2d963a3c-4d89-839e-1a66-6492fef3ab52
sex or gender	wds:Q30347924-D6F66737-B0F3-4AC6-8733-6CBF9D4628E1
VIAF ID	wds:Q30347924-f69d73a2-4e7a-ff38-e8a7-90b3ac2359c4
GND ID	wds:Q30347924-0d037731-41f8-4e43-7fbe-e8fa06df7b1c
country of citizenship	wds:Q30347924-e2969a30-4299-4781-4a38-95ebac724b28
position held	wds:Q30347924-67D2D951-3FB4-4988-B226-4766BA041BF6
date of birth	wds:Q30347924-D97E71D2-4851-4388-9E44-D2CB8B89F8AC
educated at	wds:Q30347924-4566a063-40ab-4f5c-cd8f-6c9679cfad4a
family name	wds:Q30347924-fbb8b53f-434d-5960-8e14-1e0943700b97
WorldCat Identities ID (superseded)	wds:Q30347924-EDBA1712-1C0F-4A04-92B7-A1CBA90634FE
official website	wds:Q30347924-B9D4A963-D258-4535-9C08-2004F9F3B94A
VIAF ID	http://viaf.org/viaf/317090214
GND ID	https://d-nb.info/gnd/1076507115
employer	University of Helsinki
place of birth	Seinäjoki
sex or gender	male
VIAF ID	317090214
GND ID	1076507115
country of citizenship	Finland
position held	full professor
date of birth	1970-09-21 00:00:00Z (xsd:dateTime)
educated at	University of Helsinki
family name	Raivio
WorldCat Identities ID (superseded)	viaf-317090214
official website	https://tuhat.helsinki.fi/portal/en/persons/taneli-raivio(4c4c12f5-1436-4802-ab72-043b1c75fc76).html
Springer Nature person ID	wds:Q30347924-C15F6F12-BA9F-42B8-BAEA-368C3E7F355A
ORCID iD	wds:Q30347924-6CB6B493-3FE7-42FB-9DF0-929CE79DE9DB
Dimensions author ID	wds:Q30347924-08F083EF-9A18-4E0A-8BE7-2A2677776E07
ORCID iD	https://orcid.org/0000-0001-5385-434X
Springer Nature person ID	01216240036.26
ORCID iD	0000-0001-5385-434X
Dimensions author ID	01216240036.26
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q30347924
is author of	Serum angiopoietin-like 4 protein levels and expression in adipose tissue are inversely correlated with obesity in monozygotic twins Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathy Circulating glucocorticoid bioactivity in the preterm newborn after antenatal betamethasone treatment Reversible congenital hypogonadotropic hypogonadism in patients with CHD7, FGFR1 or GNRHR mutations Incidence, phenotypic features and molecular genetics of Kallmann syndrome in Finland Impaired fibroblast growth factor receptor 1 signaling as a cause of normosmic idiopathic hypogonadotropic hypogonadism The role of gene defects underlying isolated hypogonadotropic hypogonadism in patients with constitutional delay of growth and puberty. Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism Genetic features of the X chromosome affect pubertal development and testicular degeneration in adolescent boys with Klinefelter syndrome Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism LIN28B, LIN28A, KISS1, and KISS1R in idiopathic central precocious puberty LIN28B in constitutional delay of growth and puberty. Cholesterol Metabolism Altered and FGF21 Levels High After Pediatric Liver Transplantation Despite Normal Serum Lipids Comparison of solution-based exome capture methods for next generation sequencing Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia Identification of glucocorticoid-response genes in children with acute lymphoblastic leukemia Circulating Anti-Müllerian Hormone Levels in Adult Men Are under a Strong Genetic Influence High-sensitivity C-reactive protein in paediatric inflammatory bowel disease Fecal calprotectin remains high during glucocorticoid therapy in children with inflammatory bowel disease Congenital hypogonadotropic hypogonadism, functional hypogonadotropism or constitutional delay of growth and puberty? An analysis of a large patient series from a single tertiary center Childhood growth in boys with congenital hypogonadotropic hypogonadism. Circulating antimüllerian hormone levels in boys decline during early puberty and correlate with inhibin B. Childhood growth of females with Kallmann syndrome and FGFR1 mutations. Neural crest cells: from developmental biology to clinical interventions

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