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Björn-Anders Jonsson

Umeå University

22

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1777

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Pre and postnatal growth failure with microcephaly due to two novel heterozygous IGF1R mutations and response to growth hormone treatment

2020 Acta Paediatrica
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A Missense Mutation in the Aggrecan C-type Lectin Domain Disrupts Extracellular Matrix Interactions and Causes Dominant Familial Osteochondritis Dissecans

2010 American Journal of Human Genetics
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Systematic replication study of reported genetic associations in prostate cancer: Strong support for genetic variation in the androgen pathway†

2006 The Prostate
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A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics

2005 American Journal of Human Genetics
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Comprehensive genetic evaluation of common E-cadherin sequence variants and prostate cancer risk: strong confirmation of functional promoter SNP.

2005 Human Genetics
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Characterization of a Recurrent Germ Line Mutation of the E-Cadherin Gene: Implications for Genetic Testing and Clinical Management

2005 Clinical Cancer Research
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Analysis of the macrophage scavenger receptor 1 gene in Swedish hereditary and sporadic prostate cancer

2004 The Prostate
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-160C/A polymorphism in the E-cadherin gene promoter and risk of hereditary, familial and sporadic prostate cancer.

2004 International Journal of Cancer
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Genetic analysis of the RNASEL gene in hereditary, familial, and sporadic prostate cancer

2004 Clinical Cancer Research
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Genome-wide scan of Swedish families with hereditary prostate cancer: Suggestive evidence of linkage at 5q11.2 and 19p13.3†

2003 The Prostate
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Citations (63)