Publications by authors named "Jesper Brohede"

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Biochemical studies of poly-T variants in the Alzheimer's disease associated TOMM40 gene.
Louise Hedskog, Jesper Brohede, Birgitta Wiehager, Catarina Moreira Pinho, Priya Revathikumar

J Alzheimers Dis· May 2013

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Evidence of linkage to chromosomes 10p15.3-p15.1, 14q24.3-q31.1 and 9q33.3-q34.3 in non-syndromic colorectal cancer families.
Ian W Saunders, Jason Ross, Finlay Macrae, Graeme P Young, Ignacio Blanco, Jesper Brohede

Eur J Hum Genet· January 2012

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Linkage analysis of autopsy-confirmed familial Alzheimer disease supports an Alzheimer disease locus in 8q24.
Anna Sillén, Jesper Brohede, Charlotte Forsell, Lena Lilius, Jorge Andrade

Dement Geriatr Cogn Disord· July 2011

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A DNA methylation study of the amyloid precursor protein gene in several brain regions from patients with familial Alzheimer disease.
Jesper Brohede, Mia Rinde, Bengt Winblad, Caroline Graff

J Neurogenet· December 2010

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Linkage to 20p13 including the ANGPT4 gene in families with mixed Alzheimer's disease and vascular dementia.
Anna Sillén, Jesper Brohede, Lena Lilius, Charlotte Forsell, Jorge Andrade

J Hum Genet· October 2010

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Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease.
Liesel M FitzGerald, Briony Patterson, Russell Thomson, Andrea Polanowski, Stephen Quinn, Jesper Brohede

Eur J Hum Genet· March 2009

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Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family.
Huei-Hsin Chiang, Lina Rosvall, Jesper Brohede, Karin Axelman, Behnosh F Björk

Alzheimers Dement· November 2008

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Resolution of trisomic mosaicism in prenatal diagnosis: estimated performance of a 50K SNP microarray.
Jillian Cross, Greg Peters, Zhanhe Wu, Jesper Brohede, Garry N Hannan

Prenat Diagn· December 2007

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A range of simple summary genome-wide statistics for detecting genetic linkage using high density marker data.
Ian W Saunders, Garry N Hannan, Jesper Brohede, Graham G Giles, Mark A Jenkins

Genet Epidemiol· September 2007

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Estimating genotyping error rates from Mendelian errors in SNP array genotypes and their impact on inference.
Ian W Saunders, Jesper Brohede, Garry N Hannan

Genomics· September 2007

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Evolutionary evidence suggests that CpG island-associated Alus are frequently unmethylated in human germline.
Jesper Brohede, Keith N Rand

Hum Genet· May 2006

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Chromosome 7 aberrations in a young girl with myelodysplasia and hepatoblastoma: an unusual association.
Katherine Neas, Greg Peters, Julianne Jackson, Mrinal Tembe, Zhan He Wu, Jesper Brohede

Clin Dysmorphol· January 2006

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PPC: an algorithm for accurate estimation of SNP allele frequencies in small equimolar pools of DNA using data from high density microarrays.
Jesper Brohede, Rob Dunne, James D McKay, Garry N Hannan

Nucleic Acids Res· September 2005

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Single-molecule analysis of the hypermutable tetranucleotide repeat locus D21S1245 through sperm genotyping: a heterogeneous pattern of mutation but no clear male age effect.
Jesper Brohede, Norman Arnheim, Hans Ellegren

Mol Biol Evol· January 2004

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Individual variation in microsatellite mutation rate in barn swallows.
Jesper Brohede, Anders P Møller, Hans Ellegren

Mutat Res· January 2004

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Heterogeneity in the rate and pattern of germline mutation at individual microsatellite loci.
Jesper Brohede, Craig R Primmer, Anders Møller, Hans Ellegren

Nucleic Acids Res· May 2002

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