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International Journal of Cancer|May 24, 2007
Increased HIF1 alpha in SDH and FH deficient tumors does not cause microsatellite instabilityHeli J Lehtonen, Markus J Mäkinen, Maija Kiuru, et al.
Cancer Research|August 17, 2002
Few FH mutations in sporadic counterparts of tumor types observed in hereditary leiomyomatosis and renal cell cancer familiesMaija Kiuru, Rainer Lehtonen, Johanna Arola, et al.
Genes, Chromosomes & Cancer|April 18, 2009
Array comparative genomic hybridization identifies a distinct DNA copy number profile in renal cell cancer associated with hereditary leiomyomatosis and renal cell cancerTaru A Koski, Heli J Lehtonen, Kowan J Jee, et al.
American Journal of Human Genetics|December 20, 2003
Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paragangliomaSakari Vanharanta, Mary Buchta, Sarah R McWhinney, et al.
Familial Cancer|January 22, 2010
No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndromePia Vahteristo, Taru A Koski, Laura Näätsaari, et al.
Cancer Genetics and Cytogenetics|May 28, 2008
Mutation screening of fumarate hydratase by multiplex ligation-dependent probe amplification: detection of exonic deletion in a patient with leiomyomatosis and renal cell cancerTaru Ahvenainen, Heli J Lehtonen, Rainer Lehtonen, et al.
American Journal of Human Genetics|August 23, 2016
Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset EncephalopathyMikko Muona, Ryosuke Ishimura, Anni Laari, et al.
Nature Genetics|February 28, 2002
Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancerIan P M Tomlinson, N Afrina Alam, Andrew J Rowan, et al.
Acta Neuropathologica|February 10, 2018
NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary diseaseJohanna Uusimaa, Riitta Kaarteenaho, Teija Paakkola, et al.
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