A. Flaquer

发表

Evaluation of Potential Power Gain with Imputed Genotypes in Genome-Wide Association Studies

T. Becker, C. Herold, M. Steffens, 2009, Human Heredity.

Maternal relationships within an Iron Age burial at the High Pasture Cave, Isle of Skye, Scotland

James F. Wilson, M. Pala, M. Richards, 2019, Journal of Archaeological Science.

Genetic association study of the P‐type ATPase ATP13A2 in late‐onset Parkinson's disease

K. Lohmann, A. Ramírez, S. Paus, 2009, Movement disorders : official journal of the Movement Disorder Society.

Genome-wide linkage analysis of congenital heart defects using MOD score analysis identifies two novel loci

K. Strauch, D. Heine-Suñer, J. Rosell, 2013, BMC Genetics.

First mitochondrial genome-wide association study with metabolomics

C. Gieger, S. Zöllner, K. Suhre, 2021, Human molecular genetics.

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.

S. Cichon, T. Schulze, T. Wienker, 2005, American journal of human genetics.

Biomolecular insights into North African-related ancestry, mobility and diet in eleventh-century Al-Andalus

A. Torroni, A. Achilli, M. Pala, 2021, Scientific Reports.

Susceptibility variants for male-pattern baldness on chromosome 20p11

Thomas W. Mühleisen, S. Cichon, T. Mühleisen, 2008, Nature Genetics.

The conserved ASTN2/BRINP1 locus at 9q33.1–33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain

K. Strauch, D. Heine-Suñer, G. Olmos, 2021, Scientific Reports.

Familial Psychosis Associated With a Missense Mutation at MACF1 Gene Combined With the Rare Duplications DUP3p26.3 and DUP16q23.3, Affecting the CNTN6 and CDH13 Genes

K. Strauch, D. Heine-Suñer, G. Olmos, 2021, Frontiers in Genetics.

Mitochondrial Genetic Variants Identified to Be Associated with BMI in Adults

M. Waldenberger, A. Peters, K. Strauch, 2014, PloS one.

Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait.

T. Wienker, C. Cremers, H. Kremer, 2008, American journal of human genetics.

The human pseudoautosomal regions: a review for genetic epidemiologists

T. Wienker, C. Fischer, G. Rappold, 2008, European Journal of Human Genetics.

Genome-wide linkage analysis of congenital heart defects using MOD score analysis identifies two novel loci

K. Strauch, D. Heine-Suñer, J. Rosell, 2013, BMC Genetics.

Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.

S. Cichon, M. Rietschel, M. Nöthen, 2005, American journal of human genetics.

Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26.

M. Nöthen, H. Hennies, A. Hillmer, 2008, American journal of human genetics.

Linkage analysis of alcohol dependence using MOD scores

K. Strauch, T. Wienker, M. Baur, 2005, BMC Genetics.

A new susceptibility locus for bipolar affective disorder in PAR1 on Xp22.3/Yp11.3

S. Cichon, M. Rietschel, M. Nöthen, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Loss-of-function mutations in the filaggrin gene and alopecia areata: strong risk factor for a severe course of disease in patients comorbid for atopic disease.

M. Nöthen, T. Wienker, A. Hillmer, 2007, The Journal of investigative dermatology.

Fine mapping of 10q and 18q for familial Alzheimer's disease in Caribbean Hispanics

J. H. Lee, B. Tycko, R. Mayeux, 2004, Molecular Psychiatry.

A comparison of different linkage statistics in small to moderate sized pedigrees with complex diseases

K. Strauch, A. Flaquer, 2012, BMC Research Notes.

Prediction of type 2 diabetes mellitus based on nutrition data

W. Rathmann, K. Strauch, A. Flaquer, 2021, Journal of Nutritional Science.

Mitochondrial GWA Analysis of Lipid Profile Identifies Genetic Variants to Be Associated with HDL Cholesterol and Triglyceride Levels

M. Waldenberger, A. Peters, K. Strauch, 2015, PloS one.

Genetic influences on memory performance in familial Alzheimer disease

J. H. Lee, B. Tycko, R. Mayeux, 2004, Neurology.

A New Sex-Specific Genetic Map of the Human Pseudoautosomal Regions (PAR1 and PAR2)

T. Wienker, C. Fischer, A. Flaquer, 2009, Human Heredity.

Mitochondrial genetic variants identified to be associated with posttraumatic stress disorder

M. Waldenberger, A. Peters, K. Strauch, 2015, Translational Psychiatry.

Genetic influences on life span and survival among elderly African‐Americans, Caribbean Hispanics, and Caucasians

P. Cross, R. Mayeux, N. Schupf, 2004, American journal of medical genetics. Part A.

Association study of mitochondrial genetic polymorphisms in asthmatic children.

K. Strauch, A. Heinzmann, S. Rospleszcz, 2014, Mitochondrion.

Circulating metabolites modulated by diet are associated with depression

C. Gieger, Sonja Kunze, M. Waldenberger, 2023, Molecular psychiatry.

The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata

A. Hillmer, M. Nöthen, T. Tüting, 2007, The British journal of dermatology.