Harriet von Koskull - Concepedia

Author

Harriet von Koskull

Also Known As

H von Koskull, H. (b) von Koskull, H. Koskull, H. Von Koskull, H. v. Koskull, H. von Koskull, HARRIET KOSKULL, HARRIET VON KOSKULL, Harriet Koskull, Harriet Von Koskull

Publications

Citations

H-Index

Concepts

All Affiliations

Helsinki University Hospital University of Helsinki Väestöliitto Oulu University Hospital Erasmus University Rotterdam

About

Harriet von Koskull is an author at Helsinki University Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	19	951
2	Public Health	3	3	144
3	Health Sciences	2	2	64
4	Biology	2	2	64
5	Natural Sciences	1	1	13

Harriet von Koskull

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate Alleles Sarah L. Nolin, W. Ted Brown, Anne Glicksman, The American Journal of Human Genetics Allelic VariantGenetic DisorderGeneticsFragile X SpectrumGynecology	2003	418
The 11q;22q translocation: A European collaborative analysis of 43 cases M. Fraccaro, J. Lindsten, C. E. Ford, Human Genetics European Collaborative Analysis	1980	201
The 11q;22q translocation: A collaborative study of 20 new cases and analysis of 110 families Lennart Iselius, J. Lindsten, Alain Aurias, Human Genetics Human MigrationNew CasesCollaborative Study	1983	189
Prenatally detected trisomy 7 mosaicism in a dysmorphic child Sirpa Kivirikko, Riitta Salonen, Armi Salo, Prenatal Diagnosis	2002	99
Cultured human amniotic fluid cells characterized with antibodies against intermediate filaments in indirect immunofluorescence microscopy. Ismo Virtanen, Harriet von Koskull, V.-P. Lehto, Journal of Clinical Investigation OocyteImmunocytochemical TechniqueGynecologyCell CultureCytoskeleton	1981	64
Partial trisomy 21 Perttì Aula, Jaakko Leisti, Harriet von Koskull Clinical Genetics CytogeneticsGeneticsGynecologyClinical GeneticsPublic Health	1973	64
Striking Founder Effect for the Fragile X Syndrome in Finland C Oudet, Harriet von Koskull, Ann‐Marie Nordström, European Journal of Human Genetics Family MedicineGenetic DisorderDisabilityFragile X SpectrumAbnormal Development	1993	59
<i>PAK3</i> related mental disability: Further characterization of the phenotype Maarit Peippo, Anne M. Koivisto, Teppo Särkämö, American Journal of Medical Genetics Part A	2007	57
Nonrandom distribution of chromosome breaks in Fanconi’s anemia Harriet von Koskull, Perttì Aula Cytogenetic and Genome Research BiologyKaryotype ImagingHuman KaryotypeChromosome DynamicsCytogenetics	1973	51
Induction of cytokeratin expression in human mesenchymal cells Harriet von Koskull, Ismo Virtanen Journal of Cellular Physiology	1987	48

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