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source DB	source ID	text	size	updated at	# proj.	updated_at
PubMed	14729256	Lack of a genetic association between the TNXB locus and schizophrenia in a Chinese population. A recent study demonstrated that the tenascin X (TNXB) gene was associated with schizophrenia in a Briti	1.1 KB	2025-10-02	6	-
PubMed	14755442	TNXB locus may be a candidate gene predisposing to schizophrenia. We report here on the detection of nine single nucleotide polymorphisms (SNPs) near to the NOTCH4 locus in the search for schizophreni	1.47 KB	2025-10-02	7	-
PubMed	14986105	Common variants of ACE contribute to variable age-at-onset of Alzheimer's disease. Studies on the role that genetic variation may play in a complex human disease can be empowered by an assessment of b	1.64 KB	2025-10-02	6	-
PubMed	15003442	Possible linkage of schizophrenia and bipolar affective disorder to chromosome 3q29; a follow-up. The present linkage study is a follow-up within the chromosome 3q29 region in schizophrenia and bipola	1.69 KB	2025-10-02	5	-
PubMed	15546966	Lack of association of matrix metalloproteinase 3 (MMP3) genotypes with ankylosing spondylitis susceptibility and severity. OBJECTIVE: To study the linkage and association of ankylosing spondylitis (A	1.74 KB	2025-10-02	5	-
PubMed	15007729	Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene. Developmental dyslexia, or reading disability, is a multigenic complex disease for which at least five loci, i.e. DY	1.41 KB	2025-10-02	5	-
PubMed	15010842	Imprinting status of DLK1 gene in brain tumors and lymphomas. DLK1 and GTL2 are reciprocally imprinted genes on human chromosome 14q32. DLK1 encodes a transmembrane protein that is a paternally expres	1.32 KB	2025-10-02	6	-
PubMed	15561962	Polymorphism in the calsequestrin 1 (CASQ1) gene on chromosome 1q21 is associated with type 2 diabetes in the old order Amish. Calsequestrin (CASQ)1 is involved in intracellular storage and release of	1.47 KB	2025-10-02	6	-
PubMed	15561969	Polymorphisms in both promoters of hepatocyte nuclear factor 4-alpha are associated with type 2 diabetes in the Amish. Hepatocyte nuclear factor 4-alpha (HNF4A) is a transcription factor located on ch	1.69 KB	2025-10-02	6	-
PubMed	15564288	Polymorphisms in XPD and TP53 and mutation in human lung cancer. The pattern of somatic mutations in TP53 is distinct for particular cancers and carcinogenic exposures, providing clues to disease etio	2.01 KB	2025-10-02	6	-