- ►diabetesjournals.org MG Hayes, L del Bosque-Plata, T Tsuchiya, CL Hanis, … - Diabetes, 2005 - Am Diabetes Assoc We investigated the patterns and extent of linkage disequilibrium (LD) in the vicinity of the type
2 diabetes gene calapin-10 (CAPN10) in Mexican Americans, European Americans, African
Americans, and Chinese Americans. We found that CAPN10 occurs within a single block ... Cited by 6 - Related articles - BL Direct - All 5 versions
SK Iyengar, RC Elston - Springer Summary The goal of the Human Genome Project and the subsequent HapMap Project was
to accelerate the pace at which genes for complex human traits were discovered. Elated by the
early successes from cloning disease genes for monogenic disorders, the architects of ... Related articles
H Corvol, C Flamant, C Vallet, A Clement, J Brouard - Archives de pédiatrie, 2006 - Elsevier La mucoviscidose est la plus fréquente des affections héréditaires à transmission autosomique
récessive dans les populations d'origine caucasienne, touchant environ un nouveau-né sur 4500
en France. Elle est secondaire à une mutation du gène codant pour la protéine CFTR ... Cited by 1 - Related articles - All 2 versions
[CITATION] Response to:Power dressing and meta-analysis: incorporating power analysis into …
- ►endocrinology-journals.org M Meier, HH Klein, J Kramer, M Drenckhan, … - Journal of …, 2007 - Soc Endocrinology Calpains are a family of non-lysosomal cytoplasmatic cysteine proteases. Since calpain 10
(CAPN10), a member of the calpain family of proteases, has been found to represent a putative
diabetes susceptibility gene, it was argued that calpains may be involved in the ... Cited by 1 - Related articles - BL Direct - All 2 versions
L Krause, AC McHardy, TW Nattkemper… - Nucleic Acids Research, 2007 - ukpmc.ac.uk We present the novel prokaryotic gene finder GISMO, which combines searches for protein family
domains with composition-based classification based on a support vector machine. GISMO is
highly accurate; exhibiting high sensitivity and specificity in gene identification. We found ... Cited by 1 - Related articles
X Wang, S Zhang, Q Sha - Genetic Epidemiology, 2009 - interscience.wiley.com As a result of the availability of a very large numbers of single nucleotide polymorphisms, there
has been increasing interest in genetic associations involving several closely linked loci. Methods
for detection of association between traits and multiple genetic polymorphisms are being ... Cited by 1 - Related articles - All 2 versions
W Pan - Human Heredity, 2009 - content.karger.com It is critical to develop and apply powerful statistical tests for genetic association studies due
to typically weak associations with complex human diseases or phenotypes. For population-based
case-control studies with unphased multilocus genotype data, most of the existing ... Cited by 1 - Related articles - All 3 versions
L Hsu, JR Starr, Y Zheng, SM Schwartz - Hum Hered, 2009 - content.karger.com The etiology of many common diseases such as cancer and coronary heart diseases is
complex, involving an in- terplay of both genes and environment. Researchers have collected
such comprehensive risk factor information on study participants under various design, ... Cited by 1 - Related articles - All 4 versions
