Jarmo Jääskeläinen

Author

Jarmo Jääskeläinen

Also Known As

J Jaaskelainen, J Jääskeläinen, J Jääskeläinen, J. Jaaskelainen, J. Jääskeläinen, J. Jääskeläinen, J., Jääskeläinen, Jaaskelainen J, Jarmo E. S. Jääskeläinen, Jarmo Jaaskelainen

172

Publications

Citations

H-Index

Concepts

All Affiliations

Kuopio University Hospital University of Eastern Finland University of Helsinki University of Cambridge Helsinki University Hospital

About

Jarmo Jääskeläinen is an author at Kuopio University Hospital specializing in medicine, endocrinology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	19	778
2	Education	3	3	259
3	Health Sciences	3	3	182
4	Engineering	1	1	68
5	Natural Sciences	1	1	18

Jarmo Jääskeläinen

Publications

Citations

H-Index

Page 1

	Year	Citations
Androgen Receptor Gene CAG Repeat Polymorphism in the Development of Ovarian Hyperandrogenism Lourdes Ibáñez, Ken K. Ong, Nigel P. Mongan, The Journal of Clinical Endocrinology & Metabolism	2003	184
Growth of Patients with 21-Hydroxylase Deficiency: An Analysis of the Factors Influencing Adult Height Jarmo Jääskeläinen, Raimo Voutilainen Pediatric Research Metabolic SyndromeBody CompositionGrowth HormoneMetabolic DisorderHuman Growth	1997	149
Childhood Metabolic Syndrome and Its Components in Premature Adrenarche Pauliina Utriainen, Jarmo Jääskeläinen, Jarkko Romppanen, The Journal of Clinical Endocrinology & Metabolism	2007	116
Assessment of body composition by dual‐energy <scp>X</scp>‐ray absorptiometry, bioimpedance analysis and anthropometrics in children: the <scp>P</scp>hysical <scp>A</scp>ctivity and <scp>N</scp>utrition in <scp>C</scp>hildren study Tuomo Tompuri, Timo A. Lakka, Mikko Hakulinen, Clinical Physiology and Functional Imaging	2013	97
<b>Bone mineral density in relation to glucocorticoid substitution therapy in adult patients with 21‐hydroxylase deficiency</b> Jarmo Jääskeläinen, Raimo Voutilainen Clinical Endocrinology	1996	91
Long‐term outcome of classical 21‐hydroxylase deficiency: diagnosis, complications and quality of life Jarmo Jääskeläinen, Raimo Voutilainen Acta Paediatrica	2000	87
Analysis by LC–MS/MS of endogenous steroids from human serum, plasma, endometrium and endometriotic tissue Merja R. Häkkinen, Taija Heinosalo, Niina Saarinen, Journal of Pharmaceutical and Biomedical Analysis MedicineUterine ReceptivityGynecologyFemale Reproductive FunctionMenstrual Cycle	2018	81
Detection of Novel Gene Variants Associated with Congenital Hypothyroidism in a Finnish Patient Cohort Christoffer Löf, Konrad Patyra, Teemu Kuulasmaa, Thyroid	2016	79
Simultaneous analysis by LC–MS/MS of 22 ketosteroids with hydroxylamine derivatization and underivatized estradiol from human plasma, serum and prostate tissue Merja R. Häkkinen, Teemu J. Murtola, Raimo Voutilainen, Journal of Pharmaceutical and Biomedical Analysis MedicineProstate TissueGynecologyHuman PlasmaUnderivatized Estradiol	2018	75
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism Hakan Cangül, Xiao-Hui Liao, Erik Schoenmakers, JCI Insight GeneticsMolecular BiologyMolecular GeneticsCongenital DeafnessMendelian Disorder	2018	73

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