Publications by authors named "Antonia Flaquer"

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Circulating metabolites modulated by diet are associated with depression.
Ashley van der Spek, Isobel D Stewart, Brigitte Kühnel, Maik Pietzner, Tahani Alshehri, Antonia Flaquer

Mol Psychiatry· September 2023

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First mitochondrial genome-wide association study with metabolomics.
Brahim Aboulmaouahib, Gabi Kastenmüller, Karsten Suhre, Sebastian Zöllner, Hansi Weissensteiner, Antònia Flaquer

Hum Mol Genet· September 2022

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Prediction of type 2 diabetes mellitus based on nutrition data.
Andreas Katsimpris, Aboulmaouahib Brahim, Wolfgang Rathmann, Anette Peters, Konstantin Strauch, Antònia Flaquer

J Nutr Sci· January 2022

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Biomolecular insights into North African-related ancestry, mobility and diet in eleventh-century Al-Andalus.
Marina Silva, Gonzalo Oteo-García, Rui Martiniano, João Guimarães, Matthew von Tersch, Antònia Flaquer

Sci Rep· September 2021

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The conserved ASTN2/BRINP1 locus at 9q33.1-33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain.
Josep Pol-Fuster, Francesca Cañellas, Laura Ruiz-Guerra, Aina Medina-Dols, Bàrbara Bisbal-Carrió, Antònia Flaquer

Sci Rep· July 2021

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Familial Psychosis Associated With a Missense Mutation at Gene Combined With the Rare Duplications DUP3p26.3 and DUP16q23.3, Affecting the and Genes.
Josep Pol-Fuster, Francesca Cañellas, Laura Ruiz-Guerra, Aina Medina-Dols, Bàrbara Bisbal-Carrió, Antònia Flaquer

Front Genet· April 2021

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Mitochondrial GWA Analysis of Lipid Profile Identifies Genetic Variants to Be Associated with HDL Cholesterol and Triglyceride Levels.
Antònia Flaquer, Susanne Rospleszcz, Eva Reischl, Sonja Zeilinger, Holger Prokisch

PLoS One· April 2016

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Mitochondrial genetic variants identified to be associated with BMI in adults.
Antònia Flaquer, Clemens Baumbach, Jennifer Kriebel, Thomas Meitinger, Annette Peters

PLoS One· May 2015

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Association study of mitochondrial genetic polymorphisms in asthmatic children.
Antònia Flaquer, Andrea Heinzmann, Susanne Rospleszcz, Beena Mailaparambil, Henriette Dietrich

Mitochondrion· January 2014

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Genome-wide linkage analysis of congenital heart defects using MOD score analysis identifies two novel loci.
Antònia Flaquer, Clemens Baumbach, Estefania Piñero, Fernando García Algas, María Angeles de la Fuente Sanchez

BMC Genet· May 2013

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A comparison of different linkage statistics in small to moderate sized pedigrees with complex diseases.
Antònia Flaquer, Konstantin Strauch

BMC Res Notes· August 2012

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A new susceptibility locus for bipolar affective disorder in PAR1 on Xp22.3/Yp11.3.
Antònia Flaquer, Rami Abou Jamra, Karolin Etterer, Guillermo Orozco Díaz, Fabio Rivas

Am J Med Genet B Neuropsychiatr Genet· July 2010

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A new sex-specific genetic map of the human pseudoautosomal regions (PAR1 and PAR2).
Antònia Flaquer, Christine Fischer, Thomas F Wienker

Hum Hered· September 2009

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Evaluation of potential power gain with imputed genotypes in genome-wide association studies.
Tim Becker, Antonia Flaquer, Felix F Brockschmidt, Christine Herold, Michael Steffens

Hum Hered· May 2009

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Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.
Aleksandar Rakovic, Barbara Stiller, Ana Djarmati, Antonia Flaquer, Jan Freudenberg

Mov Disord· February 2009

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Susceptibility variants for male-pattern baldness on chromosome 20p11.
Axel M Hillmer, Felix F Brockschmidt, Sandra Hanneken, Sibylle Eigelshoven, Michael Steffens, Antonia Flaquer

Nat Genet· November 2008

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Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait.
Jeroen R Huyghe, Lut Van Laer, Jan-Jaap Hendrickx, Erik Fransen, Kelly Demeester, Antonia Flaquer

Am J Hum Genet· September 2008

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The human pseudoautosomal regions: a review for genetic epidemiologists.
Antonia Flaquer, Gudrun A Rappold, Thomas F Wienker, Christine Fischer

Eur J Hum Genet· July 2008

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Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26.
Axel M Hillmer, Antonia Flaquer, Sandra Hanneken, Sibylle Eigelshoven, Anne-Katrin Kortüm

Am J Hum Genet· March 2008

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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.
Regina C Betz, Jana Pforr, Antonia Flaquer, Silke Redler, Sandra Hanneken

J Invest Dermatol· November 2007

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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.
Johannes Schumacher, Radka Kaneva, Rami Abou Jamra, Guillermo Orozco Diaz, Stephanie Ohlraun, Antonia Flaquer

Am J Hum Genet· December 2005

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Linkage analysis of alcohol dependence using MOD scores.
Konstantin Strauch, Robert Fürst, Franz Rüschendorf, Christine Windemuth, Johannes Dietter, Antonia Flaquer

BMC Genet· December 2005

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Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.
Axel M Hillmer, Sandra Hanneken, Sibylle Ritzmann, Tim Becker, Jan Freudenberg, Antonia Flaquer

Am J Hum Genet· July 2005

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Genetic influences on life span and survival among elderly African-Americans, Caribbean Hispanics, and Caucasians.
Joseph H Lee, Antonia Flaquer, Rosann Costa, Howard Andrews, Peter Cross

Am J Med Genet A· July 2004

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