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Items: 1 to 20 of 23


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

Flaquer A, Rospleszcz S, Reischl E, Zeilinger S, Prokisch H, Meitinger T, Meisinger C, Peters A, Waldenberger M, Grallert H, Strauch K.

PLoS One. 2015 May 6;10(5):e0126294. doi: 10.1371/journal.pone.0126294. eCollection 2015.


Mitochondrial genetic variants identified to be associated with posttraumatic stress disorder.

Flaquer A, Baumbach C, Ladwig KH, Kriebel J, Waldenberger M, Grallert H, Baumert J, Meitinger T, Kruse J, Peters A, Emeny R, Strauch K.

Transl Psychiatry. 2015 Mar 10;5:e524. doi: 10.1038/tp.2015.18.


Mitochondrial genetic variants identified to be associated with BMI in adults.

Flaquer A, Baumbach C, Kriebel J, Meitinger T, Peters A, Waldenberger M, Grallert H, Strauch K.

PLoS One. 2014 Aug 25;9(8):e105116. doi: 10.1371/journal.pone.0105116. eCollection 2014.


Association study of mitochondrial genetic polymorphisms in asthmatic children.

Flaquer A, Heinzmann A, Rospleszcz S, Mailaparambil B, Dietrich H, Strauch K, Grychtol R.

Mitochondrion. 2014 Jan;14(1):49-53. doi: 10.1016/j.mito.2013.11.002. Epub 2013 Nov 21.


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

Flaquer A, Baumbach C, Piñero E, García Algas F, de la Fuente Sanchez MA, Rosell J, Toquero J, Alonso-Pulpon L, Garcia-Pavia P, Strauch K, Heine-Suñer D.

BMC Genet. 2013 May 24;14:44. doi: 10.1186/1471-2156-14-44.


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

Flaquer A, Strauch K.

BMC Res Notes. 2012 Aug 6;5:411. doi: 10.1186/1756-0500-5-411.


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

Flaquer A, Jamra RA, Etterer K, Díaz GO, Rivas F, Rietschel M, Cichon S, Nöthen MM, Strauch K.

Am J Med Genet B Neuropsychiatr Genet. 2010 Jul;153B(5):1110-4. doi: 10.1002/ajmg.b.31075.


A new sex-specific genetic map of the human pseudoautosomal regions (PAR1 and PAR2).

Flaquer A, Fischer C, Wienker TF.

Hum Hered. 2009;68(3):192-200. doi: 10.1159/000224639. Epub 2009 Jun 11.


Evaluation of potential power gain with imputed genotypes in genome-wide association studies.

Becker T, Flaquer A, Brockschmidt FF, Herold C, Steffens M.

Hum Hered. 2009;68(1):23-34. doi: 10.1159/000210446. Epub 2009 Apr 1.


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

Rakovic A, Stiller B, Djarmati A, Flaquer A, Freudenberg J, Toliat MR, Linnebank M, Kostic V, Lohmann K, Paus S, Nürnberg P, Kubisch C, Klein C, Wüllner U, Ramirez A.

Mov Disord. 2009 Feb 15;24(3):429-33. doi: 10.1002/mds.22399.


Role of radiotherapy in organ-sparing treatment of seminoma.

Flaquer A, Alvarez A, Sánchez SM.

Clin Transl Oncol. 2008 Oct;10(10):679-81.


Susceptibility variants for male-pattern baldness on chromosome 20p11.

Hillmer AM, Brockschmidt FF, Hanneken S, Eigelshoven S, Steffens M, Flaquer A, Herms S, Becker T, Kortüm AK, Nyholt DR, Zhao ZZ, Montgomery GW, Martin NG, Mühleisen TW, Alblas MA, Moebus S, Jöckel KH, Bröcker-Preuss M, Erbel R, Reinartz R, Betz RC, Cichon S, Propping P, Baur MP, Wienker TF, Kruse R, Nöthen MM.

Nat Genet. 2008 Nov;40(11):1279-81. doi: 10.1038/ng.228. Epub 2008 Oct 12.


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

Huyghe JR, Van Laer L, Hendrickx JJ, Fransen E, Demeester K, Topsakal V, Kunst S, Manninen M, Jensen M, Bonaconsa A, Mazzoli M, Baur M, Hannula S, Mäki-Torkko E, Espeso A, Van Eyken E, Flaquer A, Becker C, Stephens D, Sorri M, Orzan E, Bille M, Parving A, Pyykkö I, Cremers CW, Kremer H, Van de Heyning PH, Wienker TF, Nürnberg P, Pfister M, Van Camp G.

Am J Hum Genet. 2008 Sep;83(3):401-7. doi: 10.1016/j.ajhg.2008.08.002. Epub 2008 Aug 28.


The human pseudoautosomal regions: a review for genetic epidemiologists.

Flaquer A, Rappold GA, Wienker TF, Fischer C.

Eur J Hum Genet. 2008 Jul;16(7):771-9. doi: 10.1038/ejhg.2008.63. Epub 2008 Apr 9. Review.


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

Hillmer AM, Flaquer A, Hanneken S, Eigelshoven S, Kortüm AK, Brockschmidt FF, Golla A, Metzen C, Thiele H, Kolberg S, Reinartz R, Betz RC, Ruzicka T, Hennies HC, Kruse R, Nöthen MM.

Am J Hum Genet. 2008 Mar;82(3):737-43. doi: 10.1016/j.ajhg.2007.11.014. Epub 2008 Feb 21.


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

Betz RC, König K, Flaquer A, Redler S, Eigelshoven S, Kortüm AK, Hanneken S, Hillmer A, Tüting T, Lambert J, De Weert J, Kruse R, Lutz G, Blaumeiser B, Nöthen MM.

Br J Dermatol. 2008 Feb;158(2):389-91. Epub 2007 Nov 19.


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.

Betz RC, Pforr J, Flaquer A, Redler S, Hanneken S, Eigelshoven S, Kortüm AK, Tüting T, Lambert J, De Weert J, Hillmer AM, Schmael C, Wienker TF, Kruse R, Lutz G, Blaumeiser B, Nöthen MM.

J Invest Dermatol. 2007 Nov;127(11):2539-43. Epub 2007 Jun 21.


Linkage analysis of alcohol dependence using MOD scores.

Strauch K, Fürst R, Rüschendorf F, Windemuth C, Dietter J, Flaquer A, Baur MP, Wienker TF.

BMC Genet. 2005 Dec 30;6 Suppl 1:S162.


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.

Schumacher J, Kaneva R, Jamra RA, Diaz GO, Ohlraun S, Milanova V, Lee YA, Rivas F, Mayoral F, Fuerst R, Flaquer A, Windemuth C, Gay E, Sanz S, González MJ, Gil S, Cabaleiro F, del Rio F, Perez F, Haro J, Kostov C, Chorbov V, Nikolova-Hill A, Stoyanova V, Onchev G, Kremensky I, Strauch K, Schulze TG, Nürnberg P, Gaebel W, Klimke A, Auburger G, Wienker TF, Kalaydjieva L, Propping P, Cichon S, Jablensky A, Rietschel M, Nöthen MM.

Am J Hum Genet. 2005 Dec;77(6):1102-11. Epub 2005 Nov 2.


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

Hillmer AM, Hanneken S, Ritzmann S, Becker T, Freudenberg J, Brockschmidt FF, Flaquer A, Freudenberg-Hua Y, Jamra RA, Metzen C, Heyn U, Schweiger N, Betz RC, Blaumeiser B, Hampe J, Schreiber S, Schulze TG, Hennies HC, Schumacher J, Propping P, Ruzicka T, Cichon S, Wienker TF, Kruse R, Nothen MM.

Am J Hum Genet. 2005 Jul;77(1):140-8. Epub 2005 May 18.

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