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Mitochondrial GWA Analysis of Lipid Profile Identifies Genetic Variants to Be Associated with HDL Cholesterol and Triglyceride Levels. [electronic resource] by
- Flaquer, Antònia
- Rospleszcz, Susanne
- Reischl, Eva
- Zeilinger, Sonja
- Prokisch, Holger
- Meitinger, Thomas
- Meisinger, Christa
- Peters, Annette
- Waldenberger, Melanie
- Grallert, Harald
- Strauch, Konstantin
Producer: 20160425
In:
PloS one vol. 10
Availability: No items available.
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Genome-wide linkage analysis of congenital heart defects using MOD score analysis identifies two novel loci. [electronic resource] by
- Flaquer, Antònia
- Baumbach, Clemens
- Piñero, Estefania
- García Algas, Fernando
- de la Fuente Sanchez, María Angeles
- Rosell, Jordi
- Toquero, Jorge
- Alonso-Pulpon, Luis
- Garcia-Pavia, Pablo
- Strauch, Konstantin
- Heine-Suñer, Damian
Producer: 20131017
In:
BMC genetics vol. 14
Availability: No items available.
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12.
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Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease. [electronic resource] by
- Rakovic, Aleksandar
- Stiller, Barbara
- Djarmati, Ana
- Flaquer, Antonia
- Freudenberg, Jan
- Toliat, Mohammad-Reza
- Linnebank, Michael
- Kostic, Vladimir
- Lohmann, Katja
- Paus, Sebastian
- Nürnberg, Peter
- Kubisch, Christian
- Klein, Christine
- Wüllner, Ullrich
- Ramirez, Alfredo
Producer: 20090727
In:
Movement disorders : official journal of the Movement Disorder Society vol. 24
Availability: No items available.
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13.
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Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26. [electronic resource] by
- Hillmer, Axel M
- Flaquer, Antonia
- Hanneken, Sandra
- Eigelshoven, Sibylle
- Kortüm, Anne-Katrin
- Brockschmidt, Felix F
- Golla, Astrid
- Metzen, Christine
- Thiele, Holger
- Kolberg, Susanne
- Reinartz, Roman
- Betz, Regina C
- Ruzicka, Thomas
- Hennies, Hans Christian
- Kruse, Roland
- Nöthen, Markus M
Producer: 20080328
In:
American journal of human genetics vol. 82
Availability: No items available.
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14.
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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. [electronic resource] by
- Betz, Regina C
- Pforr, Jana
- Flaquer, Antonia
- Redler, Silke
- Hanneken, Sandra
- Eigelshoven, Sibylle
- Kortüm, Anne-Katrin
- Tüting, Thomas
- Lambert, Julien
- De Weert, Jozef
- Hillmer, Axel M
- Schmael, Christine
- Wienker, Thomas F
- Kruse, Roland
- Lutz, Gerhard
- Blaumeiser, Bettina
- Nöthen, Markus M
Producer: 20071029
In:
The Journal of investigative dermatology vol. 127
Availability: No items available.
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15.
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Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia. [electronic resource] by
- Hillmer, Axel M
- Hanneken, Sandra
- Ritzmann, Sibylle
- Becker, Tim
- Freudenberg, Jan
- Brockschmidt, Felix F
- Flaquer, Antonia
- Freudenberg-Hua, Yun
- Jamra, Rami Abou
- Metzen, Christine
- Heyn, Uwe
- Schweiger, Nadine
- Betz, Regina C
- Blaumeiser, Bettina
- Hampe, Jochen
- Schreiber, Stefan
- Schulze, Thomas G
- Hennies, Hans Christian
- Schumacher, Johannes
- Propping, Peter
- Ruzicka, Thomas
- Cichon, Sven
- Wienker, Thomas F
- Kruse, Roland
- Nothen, Markus M
Producer: 20050829
In:
American journal of human genetics vol. 77
Availability: No items available.
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16.
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Susceptibility variants for male-pattern baldness on chromosome 20p11. [electronic resource] by
- Hillmer, Axel M
- Brockschmidt, Felix F
- Hanneken, Sandra
- Eigelshoven, Sibylle
- Steffens, Michael
- Flaquer, Antonia
- Herms, Stefan
- Becker, Tim
- Kortüm, Anne-Katrin
- Nyholt, Dale R
- Zhao, Zhen Zhen
- Montgomery, Grant W
- Martin, Nicholas G
- Mühleisen, Thomas W
- Alblas, Margrieta A
- Moebus, Susanne
- Jöckel, Karl-Heinz
- Bröcker-Preuss, Martina
- Erbel, Raimund
- Reinartz, Roman
- Betz, Regina C
- Cichon, Sven
- Propping, Peter
- Baur, Max P
- Wienker, Thomas F
- Kruse, Roland
- Nöthen, Markus M
Producer: 20081124
In:
Nature genetics vol. 40
Availability: No items available.
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17.
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Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait. [electronic resource] by
- Huyghe, Jeroen R
- Van Laer, Lut
- Hendrickx, Jan-Jaap
- Fransen, Erik
- Demeester, Kelly
- Topsakal, Vedat
- Kunst, Sylvia
- Manninen, Minna
- Jensen, Mona
- Bonaconsa, Amanda
- Mazzoli, Manuela
- Baur, Manuela
- Hannula, Samuli
- Mäki-Torkko, Elina
- Espeso, Angeles
- Van Eyken, Els
- Flaquer, Antonia
- Becker, Christian
- Stephens, Dafydd
- Sorri, Martti
- Orzan, Eva
- Bille, Michael
- Parving, Agnete
- Pyykkö, Ilmari
- Cremers, Cor W R J
- Kremer, Hannie
- Van de Heyning, Paul H
- Wienker, Thomas F
- Nürnberg, Peter
- Pfister, Markus
- Van Camp, Guy
Producer: 20081020
In:
American journal of human genetics vol. 83
Availability: No items available.
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18.
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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. [electronic resource] by
- Schumacher, Johannes
- Kaneva, Radka
- Jamra, Rami Abou
- Diaz, Guillermo Orozco
- Ohlraun, Stephanie
- Milanova, Vihra
- Lee, Young-Ae
- Rivas, Fabio
- Mayoral, Fermin
- Fuerst, Robert
- Flaquer, Antonia
- Windemuth, Christine
- Gay, Eudoxia
- Sanz, Sebastian
- González, Maria José
- Gil, Susana
- Cabaleiro, Francisco
- del Rio, Francisco
- Perez, Fermin
- Haro, Jesus
- Kostov, Christian
- Chorbov, Vesselin
- Nikolova-Hill, Amelia
- Stoyanova, Vessela
- Onchev, George
- Kremensky, Ivo
- Strauch, Konstantin
- Schulze, Thomas G
- Nürnberg, Peter
- Gaebel, Wolfgang
- Klimke, Ansgar
- Auburger, Georg
- Wienker, Thomas F
- Kalaydjieva, Luba
- Propping, Peter
- Cichon, Sven
- Jablensky, Assen
- Rietschel, Marcella
- Nöthen, Markus M
Producer: 20060130
In:
American journal of human genetics vol. 77
Availability: No items available.
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