Confirmation of a dyslexia susceptibility locus on chromosome 1p34‐p36 in a set of 100 Canadian families

J Tzenova, BJ Kaplan, TL Petryshen… - American Journal of …, 2004 - Wiley Online Library
… We here report results confirming the presence of a dyslexia gene on 1p34-p36 in a sample
of 100 Canadian families using both qualitative (global) and quantitative (component trait) …

The KIAA0319-Like (KIAA0319L) Gene on Chromosome 1p34 as a Candidate for Reading Disabilities

JM Couto, L Gomez, K Wigg, T Cate-Carter… - Journal of …, 2008 - Taylor & Francis
… A study conducted on 100 Canadian families with multiple … have found consistent evidence
for linkage to 1p34-36, the region … for association with RD in our sample of Canadian families. …

Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population

JC Engert, M Lemire, J Faith, D Brisson… - European journal of …, 2008 - nature.com
… Fine mapping was performed on the original genome-scan families as well as additional
family members and new families over a 70 cM region of chromosome 8, centered on the NPL …

Five children with deletions of 1p34. 3 encompassing AGO1 and AGO3

MJ Tokita, PM Chow, G Mirzaa, N Dikow… - European Journal of …, 2015 - nature.com
… 4) reside in a cluster on chromosome 1p35p34. The effects of … found to have microdeletions
of chromosomal region 1p34.3 … of closely related family members on chromosome 1p35p34. …

Genomewide linkage in a large Dutch family with intracranial aneurysms: replication of 2 loci for intracranial aneurysms to chromosome 1p36. 11-p36. 13 and Xp22. 2 …

YM Ruigrok, C Wijmenga, GJE Rinkel, R Slot, F Baas… - Stroke, 2008 - Am Heart Assoc
… The locus at 1p36.11-36.13 overlaps with the previously reported locus on chromosome
1p34.3-p36.13 (ANIB3; HUGO Nomenclature Committee) identified in a single North American …

Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings

K Zhou, P Asherson, P Sham, B Franke, RJL Anney… - Biological …, 2008 - Elsevier
… METHODS: A set of 1094 single selected Caucasian ADHD nuclear families was genotyped
… RESULTS: A significant common linkage locus was found at chromosome 1p36 with a locus…

Investigating the genomic contributions to familial intracranial aneurysms in a First Nation from Northern British Columbia

A Newman-Simmons - 2021 - open.library.ubc.ca
… although IA has been well documented in Canadian and Greenlandic Inuit. To our … several
First Nation families from a community in Northwestern British Columbia, Canada. METHODS: …

Linkage analysis of chromosome 1 with essential hypertension and blood pressure quantitative traits in Chinese families

D Ge, J Huang, W Yang, J Zhao, Y Shen… - Annals of Human …, 2005 - Wiley Online Library
… The key finding of the present study is linkage of human chromosome 1p31 with essential
hypertension in 148 Chinese hypertensive families. Moreover, we have also shown weak …

High-resolution chromosome ideogram representation of currently recognized genes for autism spectrum disorders

MG Butler, SK Rafi, AM Manzardo - International journal of molecular …, 2015 - mdpi.com
… human chromosomechromosome region or breakpoint band site can be made to inform
diagnosis and gene-based personalized care and provide genetic counselling for families

Genomewide linkage in a large Caucasian family maps a new locus for intracranial aneurysms to chromosome 13q

T Santiago-Sim, SR DePalma, KL Ju, B McDonough… - Stroke, 2009 - Am Heart Assoc
… The subject of this study is a Caucasian family (CVM family) of French-Canadian heritage (…
), including markers at previously reported IA susceptibility loci in 1p34.3–36.13, 2p13, 5p15.2…