Holmberg E - Search Results

1

Screening families with endometrial and colorectal cancers for germline mutations.

Liu T, Chen J, Salahshor S, Kuismanen S, Holmberg E, Grönberg H, Peltomäki P, Lindblom A. Liu T, et al. Among authors: holmberg e. J Med Genet. 2001 Sep;38(9):E29. doi: 10.1136/jmg.38.9.e29. J Med Genet. 2001. PMID: 11546830 Free PMC article. No abstract available.

2

DGGE screening of mutations in mismatch repair genes (hMSH2 and hMLH1) in 34 Swedish families with colorectal cancer.

Liu T, Wahlberg S, Rubio C, Holmberg E, Grönberg H, Lindblom A. Liu T, et al. Among authors: holmberg e. Clin Genet. 1998 Feb;53(2):131-5. doi: 10.1111/j.1399-0004.1998.tb02660.x. Clin Genet. 1998. PMID: 9611074

3

The use of intragenic polymorphisms in determination of the genomic relevance of whole-exon deletions in MLH1 and MSH2.

Liu T, Holmberg E, Lindblom A. Liu T, et al. Among authors: holmberg e. Clin Genet. 2001 Mar;59(3):201-2. doi: 10.1034/j.1399-0004.2001.590311.x. Clin Genet. 2001. PMID: 11260232 No abstract available.

4

MSH2 codon 322 Gly to Asp seems not to confer an increased risk for colorectal cancer susceptibility.

Liu T, Stathopoulos P, Lindblom P, Rubio C, Wasteson Arver B, Iselius L, Holmberg E, Grönberg H, Lindblom A. Liu T, et al. Among authors: holmberg e. Eur J Cancer. 1998 Nov;34(12):1981. doi: 10.1016/s0959-8049(98)00217-2. Eur J Cancer. 1998. PMID: 10023327 No abstract available.

5

Genetic epidemiology of glioma.

Malmer B, Iselius L, Holmberg E, Collins A, Henriksson R, Grönberg H. Malmer B, et al. Among authors: holmberg e. Br J Cancer. 2001 Feb 2;84(3):429-34. doi: 10.1054/bjoc.2000.1612. Br J Cancer. 2001. PMID: 11161412 Free PMC article.

6

Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus.

Kainu T, Juo SH, Desper R, Schaffer AA, Gillanders E, Rozenblum E, Freas-Lutz D, Weaver D, Stephan D, Bailey-Wilson J, Kallioniemi OP, Tirkkonen M, Syrjäkoski K, Kuukasjärvi T, Koivisto P, Karhu R, Holli K, Arason A, Johannesdottir G, Bergthorsson JT, Johannsdottir H, Egilsson V, Barkardottir RB, Johannsson O, Haraldsson K, Sandberg T, Holmberg E, Grönberg H, Olsson H, Borg A, Vehmanen P, Eerola H, Heikkila P, Pyrhönen S, Nevanlinna H. Kainu T, et al. Among authors: holmberg e. Proc Natl Acad Sci U S A. 2000 Aug 15;97(17):9603-8. doi: 10.1073/pnas.97.17.9603. Proc Natl Acad Sci U S A. 2000. PMID: 10944226 Free PMC article.

7

Identification of genomic deletions of the APC gene in familial adenomatous polyposis by two independent quantitative techniques.

Meuller J, Kanter-Smoler G, Nygren AO, Errami A, Grönberg H, Holmberg E, Björk J, Wahlström J, Nordling M. Meuller J, et al. Among authors: holmberg e. Genet Test. 2004 Fall;8(3):248-56. doi: 10.1089/gte.2004.8.248. Genet Test. 2004. PMID: 15727247

8

CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome.

Wincent J, Holmberg E, Strömland K, Soller M, Mirzaei L, Djureinovic T, Robinson K, Anderlid B, Schoumans J. Wincent J, et al. Among authors: holmberg e. Clin Genet. 2008 Jul;74(1):31-8. doi: 10.1111/j.1399-0004.2008.01014.x. Epub 2008 Apr 28. Clin Genet. 2008. PMID: 18445044

9

Genomic screening in rare disorders: New mutations and phenotypes, highlighting ALG14 as a novel cause of severe intellectual disability.

Kvarnung M, Taylan F, Nilsson D, Anderlid BM, Malmgren H, Lagerstedt-Robinson K, Holmberg E, Burstedt M, Nordenskjöld M, Nordgren A, Lundberg ES. Kvarnung M, et al. Among authors: holmberg e. Clin Genet. 2018 Dec;94(6):528-537. doi: 10.1111/cge.13448. Epub 2018 Oct 15. Clin Genet. 2018. PMID: 30221345

10

Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland.

Sarantaus L, Huusko P, Eerola H, Launonen V, Vehmanen P, Rapakko K, Gillanders E, Syrjäkoski K, Kainu T, Vahteristo P, Krahe R, Pääkkönen K, Hartikainen J, Blomqvist C, Löppönen T, Holli K, Ryynänen M, Bützow R, Borg A, Wasteson Arver B, Holmberg E, Mannermaa A, Kere J, Kallioniemi OP, Winqvist R, Nevanlinna H. Sarantaus L, et al. Among authors: holmberg e. Eur J Hum Genet. 2000 Oct;8(10):757-63. doi: 10.1038/sj.ejhg.5200529. Eur J Hum Genet. 2000. PMID: 11039575

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