Yvonne Engwall - Concepedia

Author

Yvonne Engwall

Sahlgrenska University Hospital

Also Known As

Y Engwall, Y. Engwall, Yvonne Engwall

Publications

704

Citations

H-Index

Concepts

All Affiliations

Sahlgrenska University Hospital University of Gothenburg Karolinska University Hospital Karolinska Institutet

About

Yvonne Engwall is an author at Sahlgrenska University Hospital specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	652
2	Cell Biology	2	2	151
3	Molecular Genetics	2	2	86
4	Epidemiology	1	1	31
5	Molecular Biology	1	1	189

Yvonne Engwall

Publications

695

Citations

H-Index

Page 1

	Year	Citations
Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: Cumulative risks and APC gene mutations Jan Björk, Helena I. Åkerbrant, Lennart Iselius, Gastroenterology Genetic DisorderFamilial Adenomatous PolyposisGeneticsPathologyCancer Genetics	2001	252
Parallel sequencing used in detection of mosaic mutations: Comparison with four diagnostic DNA screening techniques Anna Rohlin, Josephine Wernersson, Yvonne Engwall, Human Mutation Genetic TestingGeneticsPathologyMolecular BiologyDisease Gene Identification	2009	189
A large deletion disrupts the exon 3 transcription activation domain of the BRCA2 gene in a breast/ovarian cancer family. Margareta Nordling, Per Karlsson, Jan Wahlström, PubMed Transcriptional RegulationGene Deletion DataSomatic VariantBreast OncologyGenetics	1998	94
Inactivation of promoter 1B of APC causes partial gene silencing: evidence for a significant role of the promoter in regulation and causative of familial adenomatous polyposis Anna Rohlin, Yvonne Engwall, Kaisa Fritzell, Oncogene Adenomatous Polyposis ColiPartial Gene SilencingGenetic DisorderFamilial Adenomatous PolyposisGenetics	2011	57
Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families Gunilla Kanter-Smoler, Kaisa Fritzell, Anna Rohlin, BMC Medicine	2008	43
Novel Findings in Swedish Patients With MYH-Associated Polyposis: Mutation Detection and Clinical Characterization Gunilla Kanter-Smoler, Jan Björk, Kaisa Fritzell, Clinical Gastroenterology and Hepatology Novel FindingsAutoimmune DiseaseGenetic DisorderMedicineImmunodeficiencies	2006	31
A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques Annika Bergman, Anna Flodin, Yvonne Engwall, Familial Cancer Somatic VariantGenetic DisorderMedicineGeneticsPathology	2005	29

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