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I. Fransson · SciRah

Researcher profile · Semantic Scholar

I. Fransson

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I. Fransson — researcher profile on SciRah

h-index: 19
Works: 24
Citations: 2,159

Most-cited papers

Deregulation of the platelet-derived growth factor β-chain gene via fusion with collagen gene COL1A1 in dermatof ibrosarcoma protuberans and giant-cell fibroblastoma
M. Simon, F. Pedeutour, N. Sirvent, J. Grosgeorge +13 more
1997Nature Genetics529 citations
Semantic Scholar
Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development.
M. Peyrard-Janvid, E. Leslie, Y. Kousa, Tiffany L Smith +17 more
2014American Journal of Human Genetics221 citations Open access
Semantic Scholar
High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH.
C. Bruder, C. Hirvelä, I. Tapia-Páez, I. Fransson +30 more
2001Human Molecular Genetics175 citations Open access
Semantic Scholar
Genome-Wide Analysis of Single Nucleotide Polymorphisms Uncovers Population Structure in Northern Europe
E. Salmela, T. Lappalainen, I. Fransson, P. Andersen +7 more
2008PLoS ONE163 citations Open access
Semantic Scholar
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.
P. Buckley, K. Mantripragada, Magdalena Benetkiewicz, I. Tapia-Páez +27 more
2002Human Molecular Genetics149 citations
Semantic Scholar
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.
H. Anthoni, M. Zucchelli, H. Matsson, B. Müller-Myhsok +13 more
2007Human Molecular Genetics132 citations
Semantic Scholar
The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family.
M. Peyrard, Eyal Seroussi, A. Sandberg-Nordqvist, Ya-Gang Xie +7 more
1999Proceedings of the National Academy of Sciences of the United States of America127 citations Open access
Semantic Scholar
Characterization of a new member of the human beta-adaptin gene family from chromosome 22q12, a candidate meningioma gene.
M. Peyrard, I. Fransson, Ya-Gang Xie, Fei-Yu Han +6 more
1994Human Molecular Genetics106 citations
Semantic Scholar
Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups.
H. Jiao, B. Tóth, Melinda Erdős, I. Fransson +14 more
2008Molecular Immunology87 citations Open access
Semantic Scholar
Submicroscopic genomic alterations in Silver–Russell syndrome and Silver–Russell-like patients
Sara Bruce, K. Hannula-Jouppi, M. Puoskari, I. Fransson +3 more
2009Journal of Medical Genetics80 citations
Semantic Scholar
Analysis of short stature homeobox-containing gene (SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity
G. Grigelioniene, J. Schoumans, L. Neumeyer, S. Ivarsson +15 more
2001Human Genetics58 citations
Semantic Scholar
Characterization of the human synaptogyrin gene family
D. Kedra, H. Pan, E. Seroussi, I. Fransson +7 more
1998Human Genetics56 citations
Semantic Scholar
The genes for oncostatin M (OSM) and leukemia inhibitory factor (LIF) are tightly linked on human chromosome 22.
Timothy M. Rose, Michelle J. Lagrou, I. Fransson, Barbro Werelius +5 more
1993Genomics53 citations
Semantic Scholar
Familial non-syndromic cleft lip and palate--analysis of the IRF6 gene and clinical phenotypes.
Marie Pegelow, M. Peyrard-Janvid, M. Zucchelli, I. Fransson +4 more
2008European Journal of Orthodontics45 citations
Semantic Scholar
Association and Mutation Analyses of the IRF6 Gene in Families with Nonsyndromic and Syndromic Cleft Lip and/or Cleft Palate
Marie Pegelow, H. Koillinen, M. Magnusson, I. Fransson +4 more
2014The Cleft Palate-Craniofacial Journal31 citations
Semantic Scholar
The germinal center kinase gene and a novel CDC25-like gene are located in the vicinity of the PYGM gene on 11q13
D. Kedra, E. Seroussi, I. Fransson, J. Trifunovic +5 more
1997Human Genetics31 citations
Semantic Scholar
A 1-Mb PAC contig spanning the common eliminated region 1 (CER1) in microcell hybrid-derived SCID tumors.
Ying Yang, H. Kiss, M. Kost-Alimova, D. Kedra +11 more
1999Genomics30 citations
Semantic Scholar
Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome
M. Peyrard-Janvid, Marie Pegelow, H. Koillinen, C. Larsson +6 more
2005European Journal of Human Genetics28 citations
Semantic Scholar
A novel gene containing LIM domains (LIMD1) is located within the common eliminated region 1 (C3CER1) in 3p21.3
H. Kiss, D. Kedra, Ying Yang, M. Kost-Alimova +6 more
1999Human Genetics19 citations
Semantic Scholar
Strong conservation of the human NF2 locus based on sequence comparison in five species
Caisa M. Hansson, Haider Ali, C. Bruder, I. Fransson +5 more
2003Mammalian Genome12 citations
Semantic Scholar
Physical mapping of the NF2/meningioma region on human chromosome 22q12.
M. Ruttledge, Ya-Gang Xie, Fei-Yu Han, Marco Giovannini +7 more
1994Genomics12 citations
Semantic Scholar
Cloning, expression pattern, and chromosomal assignment to 16q23 of the human γ-adaptin gene (ADTG)
M. Peyrard, S. Parveneh, S. Lagercrantz, M. Ekman +3 more
19988 citations
Semantic Scholar
Cloning, expression pattern, and chromosomal assignment to 16q23 of the human gamma-adaptin gene (ADTG).
M. Peyrard, S. Parveneh, S. Lagercrantz, M. Ekman +3 more
1998Genomics5 citations
Semantic Scholar
Characterization of the mouse beta-prime adaptin gene; cDNA sequence, genomic structure, and chromosomal localization
C. Guilbaud, M. Peyrard, I. Fransson, S. Clifton +3 more
1997Mammalian Genome4 citations
Semantic Scholar

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