Ingegerd Fransson - Concepedia

Author

Ingegerd Fransson

Karolinska University Hospital

Also Known As

I. Fransson, Ingegerd Fransson

Publications

3.1K

Citations

H-Index

Concepts

All Affiliations

Karolinska University Hospital Karolinska Institutet University of Helsinki University of Oklahoma Folkhälsans Forskningscentrum

About

Ingegerd Fransson is an author at Karolinska University Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	14	2.2K
2	Natural Sciences	3	3	1.2K
3	Public Health	1	1	54
4	Social Sciences	1	1	121
5	Biology	1	1	1.2K

Ingegerd Fransson

Publications

Citations

H-Index

Page 1

	Year	Citations
The DNA sequence of human chromosome 22 Ian Dunham, Adrienne Hunt, John Collins, Nature Comparative GenomicsGeneticsMolecular GeneticsGenomicsMolecular Ecology	1999	1.2K
Deregulation of the platelet-derived growth factor β-chain gene via fusion with collagen gene COL1A1 in dermatof ibrosarcoma protuberans and giant-cell fibroblastoma Marie-Pierre Simon, Florence Pédeutour, Nicolas Sirvent, Nature Genetics Giant-cell FibroblastomaPathologyDermatof Ibrosarcoma ProtuberansFibroblast Growth FactorCell Proliferation	1997	526
Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development Myriam Peyrard‐Janvid, Elizabeth J. Leslie, Youssef A. Kousa, The American Journal of Human Genetics	2013	227
Genome-Wide Analysis of Single Nucleotide Polymorphisms Uncovers Population Structure in Northern Europe Elina Salmela, Tuuli Lappalainen, Ingegerd Fransson, PLoS ONE	2008	184
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia Heidi Anthoni, Marco Zucchelli, Hans Matsson, Human Molecular Genetics GeneticsCandidate Susceptibility GenesMolecular GeneticsDisease Gene IdentificationSocial Sciences	2007	121
The human <i>LARGE</i> gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family Myriam Peyrard, Eyal Seroussi, Ann-Christin Sandberg-Nordqvist, Proceedings of the National Academy of Sciences	1999	118
Submicroscopic genomic alterations in Silver–Russell syndrome and Silver–Russell-like patients Katariina Hannula‐Jouppi, M. Puoskari, Ingegerd Fransson, Journal of Medical Genetics	2009	113
Characterization of a new member of the human /-adaptin gene family from chromosome 22q12, a candidate meningioma gene Myriam Peyrard, Ingegerd Fransson, Ya‐Gang Xie, Human Molecular Genetics	1994	99
A novel gene containing LIM domains (LIMD1) is located within the common eliminated region 1 (C3CER1) in 3p21.3 Hajnalka Kiss, Darek Kedra, Ying Yang, Human Genetics Novel GeneNatural SciencesGeneticsLim DomainsGene Regulation	1999	61
Characterization of the human synaptogyrin gene family Darek Kedra, Huaqin Pan, Eyal Seroussi, Human Genetics Molecular NeuroscienceMolecular NeurobiologyMedicineCell BiologyCellular Neurobiology	1998	60

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