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1
Polygenic prediction of body mass index and obesity through the life course and across ancestries

von Smit RAJ ; Wade KH ; Hui Q ; et al.

Schlagworte: Polygenic score; body mass index
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2
Immunogenicity and safety of AZD2816, a beta (B.1.351) variant COVID-19 vaccine, and AZD1222 (ChAdOx1 nCoV-19) as third-dose boosters for previously vaccinated adults: a multicentre, randomised, partly double-blinded, phase 2/3 non-inferiority immunobridging study in the UK and Poland

von Wildman, Eden ; Rampling, Tommy ; Morris, Sheila ; et al.

In The Lancet Microbe November 2023 4(11):e863-e874
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3
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

von Walsh, Roddy ; Lahrouchi, Najim ; Tadros, Rafik ; et al.

In Genetics in Medicine January 2021 23(1):47-58
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4
A Saturated Map of Common Genetic Variants Associated with Human Height

von Yengo, Loïc ; Vedantam, Sailaja ; Miao, Jenkai ; et al.

Schlagworte: common single-nucleotide polymorphisms (SNPs); human height; genome; ancestry
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5
A saturated map of common genetic variants associated with human height.

von Yengo, L ; Vedantam, S ; Marouli, E ; et al.
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6
Genome-wide association analyses identify novel Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

von Barc J, Tadros R, Glinge C, Chiang DY, Jouni M, Simonet F, Jurgens SJ, Baudic M, Nicastro M, Potet F, Offerhaus JA, Walsh R, Choi SH, Verkerk AO, Mizusawa Y, Anys S, Minois D, Arnaud M, Duchateau J, Wijeyeratne YD, Muir A, Papadakis M, Castelletti S, Torchio M, Gil Ortuño C, Lacunza J, Giachino DF, Cerrato N, Martins RP, Campuzano O, Van Dooren S, Thollet A, Kyndt F, Mazzanti A, Clémenty N, Bisson A, Corveleyn A, Stallmeyer B, Dittmann S, Saenen J, Noël A, Honarbakhsh S, Rudic B, Marzak H, Rowe MK, Federspiel C, Le Page S, Placide L, Milhem A, Barajas-Martinez H, Beckmann BM, Krapels IP, Steinfurt J, Gregers Winkel B, Jabbari R, Shoemaker MB, Boukens BJ, Škorić-Milosavljević D, Bikker H, Manevy FC, Lichtner P, Ribasés M, Meitinger T, Müller-Nurasyid M, Veldink JH, van den Berg LH, Van Damme P, Cusi D, Lanzani C, Rigade S, Charpentier E, Baron E, Bonnaud S, Lecointe S, Donnart A, Le Marec H, Chatel S, Karakachoff M, Bézieau S, London B, Tfelt-Hansen J, Roden D, Odening KE, Cerrone M, Chinitz LA, Volders PG, van de Berg MP, Laurent G, Faivre L, Antzelevitch C, Kääb S, Al Arnaout A, Dupuis JM, Pasquie JL, Billon O, Roberts JD, Jesel L, Borggrefe M, Lambiase PD, Mansourati J, Loeys B, Leenhardt A, Guicheney P, Maury P, Schulze-Bahr E, Robyns T, Breckpot J, Babuty D, Priori SG, Napolitano C, de Asmundis C, Brugada P, Brugada R, Arbelo E, Brugada J, Mabo P, Behar N, Giustetto C, Molina M, Gimeno JR, Hasdemir C, Schwartz PJ, Crotti L, McKeown PP, Sharma S, Behr ER, Haissaguerre M, Sacher F, Rooryck C, Tan HL, Remme CA, Postema PG, Delmar M, Ellinor PT, Lubitz SA, Gourraud JB, Tanck MW, George Jr. AL, MacRae CA, Burridge PW, Dina C, Probst V, Wilde AA, Schott JJ, Redon R, Bezzina CR.
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7
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

von Barc, J ; Tadros, R ; Glinge, C ; et al.

Nature Genetics , 54 (3) pp. 232-239. (2022)

Schlagworte: Genome-wide association studies; Ventricular fibrillation
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8
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.

von Young, WJ ; Lahrouchi, N ; Isaacs, A ; et al.
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9
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.

von Walsh, R ; Lahrouchi, N ; Tadros, R ; et al.
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10
Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome

von Lahrouchi N ; Tadros R ; Crotti L ; et al.

Schlagworte: genome-wide association study; inheritance pattern; long QT syndrome; Settore BIOS-14/A - Genetica; Settore MEDS-24/A - Statistica medica; Settore MEDS-07/B - Malattie dell'apparato cardiovascolare
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11
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition

von Roberts JD ; Asaki SY ; Mazzanti A ; et al.

Schlagworte: arrhythmia; genetic; long QT syndrome; penetrance; sudden cardiac death; Settore BIOS-14/A - Genetica; Settore MEDS-07/B - Malattie dell'apparato cardiovascolare
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12
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

von Ntalla, I ; Weng, L-C ; Cartwright, JH ; et al.
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13
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

von Walsh, R ; Lahrouchi, N ; Tadros, R ; et al.

Genetics in Medicine (2020) (In press).

Schlagworte: variant interpretation; LQTS; Brugada; ACMG/AMP guidelines
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14
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition

von Roberts, JD ; Asaki, SY ; Mazzanti, A ; et al.

Circulation , 141 (6) pp. 429-439. (2020)

Schlagworte: Arrhythmia; genetics; long QT syndrome; penetrance; sudden cardiac death
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15
Early mobilization in the critical care unit: A review of adult and pediatric literature

von Cameron, Saoirse ; Ball, Ian ; Cepinskas, Gediminas ; et al.

In Journal of Critical Care August 2015 30(4):664-672
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16
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.

von Lahrouchi, N ; Tadros, R ; Crotti, L ; et al.
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17
Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes

von Pulit, SL ; Weng, L-C ; McArdle, PF ; et al.
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18
Multi-ethnic genome-wide association study for atrial fibrillation

von Roselli, C ; Chaffin, MD ; Weng, L-C ; et al.
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19
Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium

von Weng, LC ; Lunetta, KL ; Muller-Nurasyid, M ; et al.

Weng, LC, Lunetta, KL, Muller-Nurasyid, M, Smith, AV, Theriault, S, Weeke, PE, Barnard, J, Bis, JC, Lyytikainen, LP, Kleber, ME, Martinsson, A, Lin, H J, Rienstra, M, Trompet, S, Krijthe, B, Dorr, M, Klarin, D, Chasman, DI, Sinner, MF, Waldenberger, M, Launer, LJ, Harris, TB, Soliman, EZ, Alonso, A, Pare, G, Teixeira, PL, Denny, JC, Shoemaker, MB, Van Wagoner, DR, Smith, JD, Psaty, BM, Sotoodehnia, N, Taylor, KD, Kahonen, M, Nikus, K, Delgado, GE, Melander, O, Engstrom, G, Yao, J, Guo, XQ, Christophersen, IE, Ellinor, PT, Geelhoed, B, Verweij, N, Macfarlane, P, Ford, I, Heeringa, J, Franco Duran, OH, ....

Schlagworte: /dk/atira/pure/keywords/researchprograms/AFL001000/EMCNIHES016401; name=EMC NIHES-01-64-01
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20
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

von Christophersen, IE ; Rienstra, M ; Roselli, C ; et al.
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21
Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium

von Weng, L-C ; Lunetta, KL ; Mueller-Nurasyid, M ; et al.

Scientific Reports , 7 , Article 11303. (2017)

Schlagworte: Cardiology; Genome-wide association studies
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22
Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.

von Barc, J ; Tadros, R ; Glinge, C ; et al.
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23
Management of Congenital Long-QT Syndrome: Commentary From the Experts

von Kaufman, ES ; Eckhardt, LL ; Ackerman, MJ ; et al.
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24
Genetic susceptibility for atrial fibrillation in patients undergoing atrial fibrillation ablation

von Shoemaker MB ; Husser D ; Roselli C ; et al.

Schlagworte: Settore MED/11
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25
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition

von Roberts, J ; Asaki, S ; Mazzanti, A ; et al.

Schlagworte: arrhythmia; genetic; long QT syndrome; penetrance; sudden cardiac death; Settore BIOS-14/A - Genetica; Settore MEDS-07/B - Malattie dell'apparato cardiovascolare; info:eu-repo/semantics/article
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