Jesper Brohede

发表

A range of simple summary genome‐wide statistics for detecting genetic linkage using high density marker data

G. Giles, J. Hopper, M. Southey, 2007, Genetic epidemiology.

A DNA Methylation Study of the Amyloid Precursor Protein Gene in Several Brain Regions from Patients with Familial Alzheimer Disease

B. Winblad, C. Graff, Mia Rinde, 2010, Journal of neurogenetics.

Individual variation in microsatellite mutation rate in barn swallows.

H. Ellegren, A. Møller, Jesper Brohede, 2004, Mutation research.

Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease

J. Dickinson, L. FitzGerald, A. Polanowski, 2009, European Journal of Human Genetics.

Evolutionary evidence suggests that CpG island-associated Alus are frequently unmethylated in human germline

K. Rand, Jesper Brohede, 2006, Human Genetics.

Chromosome 7 aberrations in a young girl with myelodysplasia and hepatoblastoma: an unusual association

G. Peters, G. N. Hannan, F. Collins, 2006, Clinical dysmorphology.

Linkage to 20p13 including the ANGPT4 gene in families with mixed Alzheimer's disease and vascular dementia

B. Winblad, J. Odeberg, C. Graff, 2010, Journal of Human Genetics.

Resolution of trisomic mosaicism in prenatal diagnosis: estimated performance of a 50K SNP microarray

G. Peters, G. N. Hannan, Zhanhe Wu, 2007, Prenatal diagnosis.

Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family

C. Graff, Huei-Hsin Chiang, K. Axelman, 2008, Alzheimer's & Dementia.

Estimating genotyping error rates from Mendelian errors in SNP array genotypes and their impact on inference.

G. N. Hannan, Ian W Saunders, Jesper Brohede, 2007, Genomics.

Brohede, J. 2003. Rates and Patterns of Mutation in Microsatellite DNA. Acta Universitatis Upsaliensis. Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 803. 51 pp. Uppsala. ISBN 91-554-5524-7

Jesper Brohede, 2003 .

List of Thesis Papers Papers I-iv Are Available in Appendix 1 Individual Variation in Microsatellite Mutation Rate in Barn Swallows. (manuscript) Summaries of Papers including Discussion.. 26

H. Ellegren, A. Møller, N. Arnheim, 2022 .

Single-molecule analysis of the hypermutable tetranucleotide repeat locus D21S1245 through sperm genotyping: a heterogeneous pattern of mutation but no clear male age effect.

H. Ellegren, N. Arnheim, Jesper Brohede, 2003, Molecular biology and evolution.

Microsatellite evolution: polarity of substitutions within repeats and neutrality of flanking sequences

H. Ellegren, Jesper Brohede, 1999, Proceedings of the Royal Society of London. Series B: Biological Sciences.

Heterogeneity in the rate and pattern of germline mutation at individual microsatellite loci.

H. Ellegren, A. Møller, C. Primmer, 2002, Nucleic acids research.

Linkage Analysis of Autopsy-Confirmed Familial Alzheimer Disease Supports an Alzheimer Disease Locus in 8q24

B. Winblad, J. Odeberg, C. Graff, 2011, Dementia and Geriatric Cognitive Disorders.

PPC: an algorithm for accurate estimation of SNP allele frequencies in small equimolar pools of DNA using data from high density microarrays

G. N. Hannan, Jesper Brohede, R. Dunne, 2005, Nucleic acids research.

Evidence of linkage to chromosomes 10p15.3–p15.1, 14q24.3–q31.1 and 9q33.3–q34.3 in non-syndromic colorectal cancer families

V. Moreno, G. Capellá, G. N. Hannan, 2011, European Journal of Human Genetics.

Biochemical studies of poly-T variants in the Alzheimer's disease associated TOMM40 gene.

C. Graff, M. Ankarcrona, C. Pinho, 2012, Journal of Alzheimer's disease : JAD.

Extrapair paternity in relation to sexual ornamentation, arrival date, and condition in a migratory bird

A. Møller, C. Primmer, F. Lope, 2003 .

Methylation studies in brains from patients with familial Alzheimer's disease

B. Winblad, C. Graff, Jesper Brohede, 2009, Alzheimer's & Dementia.