Associated Papers
Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy.
Takata A et al.
Nature Communications, 2019
31175295 (PubMed )
Supplement: 41467_2019_10482_MOESM8_ESM.xlsx › Supplementary_Data_5
Association of the ARLTS1 variants with familial ovarian cancer risk in China.
Yang XY et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society, 2009
ARLTS1 germline variants and the risk for breast, prostate, and colorectal cancer.
Siltanen S et al.
European Journal of Human Genetics : Ejhg, 2008
No association of ARLTS1 polymorphisms and risk for familial chronic lymphocytic leukaemia.
Ng D et al.
British Journal of Haematology, 2007
ARLTS1 polymorphisms and basal cell carcinoma of the skin.
Li X et al.
Hereditary Cancer in Clinical Practice, 2007
Relationship between ARLTS1 polymorphisms and risk of chronic lymphocytic leukemia.
Sellick GS et al.
Leukemia Research, 2006
Association of the ARLTS1 Cys148Arg variant with familial breast cancer risk.
Frank B et al.
International Journal of Cancer, 2006
Familial cancer associated with a polymorphism in ARLTS1.
Calin GA et al.
The New England Journal of Medicine, 2005
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