Nina Horelli‐Kuitunen

Author

Also Known As

Katja Aktan-Collan, N Horelli-Kuitunen, N Horelli‐Kuitunen, N. Horelli-Kuitunen, Nina Horelli-Kuitunen, Nina Horelli‐Kuitunen, Nina Horelli–Kuitunen

Publications

2.8K

Citations

H-Index

Concepts

All Affiliations

University of Helsinki Helsinki University Hospital Institute for Molecular Medicine Finland University of Oulu Väestöliitto

About

Nina Horelli‐Kuitunen is an author at University of Helsinki specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	16	1.8K
2	Natural Sciences	6	6	133
3	Public Health	2	2	290
4	Biochemistry	2	2	61
5	Social Sciences	1	1	10

Nina Horelli‐Kuitunen

Publications

2.8K

Citations

H-Index

Page 1

	Year	Citations
An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains Johanna Aaltonen, Petra Björses, Jaakko Perheentupa, Nature Genetics Autoimmune DiseaseNovel GeneAutoantibody ProductionDisease MechanismImmunology	1997	1.2K
Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies Francesca Romana Grati, D. Molina Gomes, José Carlos Ferreira, Prenatal Diagnosis	2015	303
Human Growth Differentiation Factor 9 (GDF-9) and Its Novel Homolog GDF-9B Are Expressed in Oocytes during Early Folliculogenesis<sup>1</sup> Johanna Aaltonen, Mika Laitinen, Kaisa Vuojolainen, The Journal of Clinical Endocrinology & Metabolism Gdf-9 TranscriptOocyteFertilityGdf-9 MrnaGenetics	1999	274
Chromosomal Location, Exon Structure, and Vascular Expression Patterns of the Human <i>PDGFC</i> and <i>PDGFD</i> Genes Marko Uutela, Juha Laurén, Erika Bergsten, Circulation	2001	133
Novel Human Vascular Endothelial Growth Factor Genes VEGF-B and VEGF-C Localize to Chromosomes 11q13 and 4q34, Respectively Karri Paavonen, Nina Horelli‐Kuitunen, Dimitri Chilov, Circulation	1996	105
Two cases of Y; autosome translocations: A 45, X male and a clinically trisomy 18 patient Solange B. Farah, Clarisa F. Ramos, Maricilda Palandi de Mello, American Journal of Medical Genetics	1994	82
Distinct differentiation characteristics of individual human embryonic stem cell lines Milla Mikkola, Cia Olsson, Jaan Palgi, BMC Developmental Biology	2006	71
Prenatal diagnosis of 24 cases of microduplication 22q11.2: an investigation of phenotype-genotype correlations Céline Dupont, Francesca Romana Grati, Kwong Wai Choy, Prenatal Diagnosis	2014	65
High-Resolution Physical and Transcriptional Mapping of the Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy Locus on Chromosome 21q22.3 by FISH Johanna Aaltonen, Nina Horelli‐Kuitunen, Jian‐Bing Fan, Genome Research	1997	60
Genetic Aberrations in Sporadic and Neurofibromatosis 2 (NF2)-Associated Schwannomas Studied by Comparative Genomic Hybridization (CGH) J. Antinheimo, Satu‐Leena Sallinen, P Sallinen, Acta Neurochirurgica Neuro-oncologySomatic VariantGenetic DisorderMedicineGenetics	2000	54

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