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Items: 1 to 50 of 57

1.

Is High-Density Lipoprotein Cholesterol Causally Related to Kidney Function? Evidence From Genetic Epidemiological Studies.

Coassin S, Friedel S, Köttgen A, Lamina C, Kronenberg F.

Arterioscler Thromb Vasc Biol. 2016 Nov;36(11):2252-2258. Epub 2016 Sep 29.

2.

A genome-wide association meta-analysis on apolipoprotein A-IV concentrations.

Lamina C, Friedel S, Coassin S, Rueedi R, Yousri NA, Seppälä I, Gieger C, Schönherr S, Forer L, Erhart G, Kollerits B, Marques-Vidal P, Ried J, Waeber G, Bergmann S, Dähnhardt D, Stöckl A, Kiechl S, Raitakari OT, Kähönen M, Willeit J, Kedenko L, Paulweber B, Peters A, Meitinger T, Strauch K; KORA Study Group, Lehtimäki T, Hunt SC, Vollenweider P, Kronenberg F.

Hum Mol Genet. 2016 Aug 15;25(16):3635-3646. doi: 10.1093/hmg/ddw211. Epub 2016 Jul 12.

3.

The low molecular weight fraction of compounds released from immature wheat pistils supports barley pollen embryogenesis.

Lippmann R, Friedel S, Mock HP, Kumlehn J.

Front Plant Sci. 2015 Jul 7;6:498. doi: 10.3389/fpls.2015.00498. eCollection 2015.

4.

Dispositional mindfulness is predicted by structural development of the insula during late adolescence.

Friedel S, Whittle SL, Vijayakumar N, Simmons JG, Byrne ML, Schwartz OS, Allen NB.

Dev Cogn Neurosci. 2015 Aug;14:62-70. doi: 10.1016/j.dcn.2015.07.001. Epub 2015 Jul 9.

5.

Dissecting spatiotemporal biomass accumulation in barley under different water regimes using high-throughput image analysis.

Neumann K, Klukas C, Friedel S, Rischbeck P, Chen D, Entzian A, Stein N, Graner A, Kilian B.

Plant Cell Environ. 2015 Oct;38(10):1980-96. doi: 10.1111/pce.12516. Epub 2015 Apr 14.

PMID:
25689277
6.

Dissecting the phenotypic components of crop plant growth and drought responses based on high-throughput image analysis.

Chen D, Neumann K, Friedel S, Kilian B, Chen M, Altmann T, Klukas C.

Plant Cell. 2014 Dec;26(12):4636-55. doi: 10.1105/tpc.114.129601. Epub 2014 Dec 11.

7.

A novel noninvasive procedure for high-throughput screening of major seed traits.

Rolletschek H, Fuchs J, Friedel S, Börner A, Todt H, Jakob PM, Borisjuk L.

Plant Biotechnol J. 2015 Feb;13(2):188-99. doi: 10.1111/pbi.12245. Epub 2014 Sep 9.

8.

Separating the wheat from the chaff - a strategy to utilize plant genetic resources from ex situ genebanks.

Keilwagen J, Kilian B, Özkan H, Babben S, Perovic D, Mayer KF, Walther A, Poskar CH, Ordon F, Eversole K, Börner A, Ganal M, Knüpffer H, Graner A, Friedel S.

Sci Rep. 2014 Jun 10;4:5231. doi: 10.1038/srep05231.

9.

Arabidopsis kinetochore null2 is an upstream component for centromeric histone H3 variant cenH3 deposition at centromeres.

Lermontova I, Kuhlmann M, Friedel S, Rutten T, Heckmann S, Sandmann M, Demidov D, Schubert V, Schubert I.

Plant Cell. 2013 Sep;25(9):3389-404. doi: 10.1105/tpc.113.114736. Epub 2013 Sep 6.

10.

Plasticity of the Arabidopsis root system under nutrient deficiencies.

Gruber BD, Giehl RF, Friedel S, von Wirén N.

Plant Physiol. 2013 Sep;163(1):161-79. doi: 10.1104/pp.113.218453. Epub 2013 Jul 12.

11.

Patterns of nucleotide asymmetries in plant and animal genomes.

Mascher M, Schubert I, Scholz U, Friedel S.

Biosystems. 2013 Mar;111(3):181-9. doi: 10.1016/j.biosystems.2013.02.001. Epub 2013 Feb 21.

PMID:
23438636
12.

[Leopard-spot pattern in fluorescein angiography].

Friedel S, Polak A.

Ophthalmologe. 2013 Apr;110(4):360-4. doi: 10.1007/s00347-012-2771-0. German.

PMID:
23338531
13.

Reverse engineering: a key component of systems biology to unravel global abiotic stress cross-talk.

Friedel S, Usadel B, von Wirén N, Sreenivasulu N.

Front Plant Sci. 2012 Dec 31;3:294. doi: 10.3389/fpls.2012.00294. eCollection 2012.

14.

Heterosis manifestation during early Arabidopsis seedling development is characterized by intermediate gene expression and enhanced metabolic activity in the hybrids.

Meyer RC, Witucka-Wall H, Becher M, Blacha A, Boudichevskaia A, Dörmann P, Fiehn O, Friedel S, von Korff M, Lisec J, Melzer M, Repsilber D, Schmidt R, Scholz M, Selbig J, Willmitzer L, Altmann T.

Plant J. 2012 Aug;71(4):669-83. doi: 10.1111/j.1365-313X.2012.05021.x. Epub 2012 Jun 12.

15.

Differentiation of endosperm transfer cells of barley: a comprehensive analysis at the micro-scale.

Thiel J, Riewe D, Rutten T, Melzer M, Friedel S, Bollenbeck F, Weschke W, Weber H.

Plant J. 2012 Aug;71(4):639-55. doi: 10.1111/j.1365-313X.2012.05018.x. Epub 2012 Jun 20.

16.

Seed-specific elevation of non-symbiotic hemoglobin AtHb1: beneficial effects and underlying molecular networks in Arabidopsis thaliana.

Thiel J, Rolletschek H, Friedel S, Lunn JE, Nguyen TH, Feil R, Tschiersch H, Müller M, Borisjuk L.

BMC Plant Biol. 2011 Mar 15;11:48. doi: 10.1186/1471-2229-11-48.

17.

TassDB2 - A comprehensive database of subtle alternative splicing events.

Sinha R, Lenser T, Jahn N, Gausmann U, Friedel S, Szafranski K, Huse K, Rosenstiel P, Hampe J, Schuster S, Hiller M, Backofen R, Platzer M.

BMC Bioinformatics. 2010 Apr 29;11:216. doi: 10.1186/1471-2105-11-216.

18.

Functional variants of the serotonin receptor type 3A and B gene are associated with eating disorders.

Hammer C, Kapeller J, Endele M, Fischer C, Hebebrand J, Hinney A, Friedel S, Gratacòs M, Estivill X, Fichter M, Fernández-Aranda F, Ehrlich S, Rappold G, Niesler B.

Pharmacogenet Genomics. 2009 Oct;19(10):790-9. doi: 10.1097/FPC.0b013e32833132b3.

PMID:
19741568
19.

Familiality and molecular genetics of attention networks in ADHD.

Konrad K, Dempfle A, Friedel S, Heiser P, Holtkamp K, Walitza S, Sauer S, Warnke A, Remschmidt H, Gilsbach S, Schäfer H, Hinney A, Hebebrand J, Herpertz-Dahlmann B.

Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):148-58. doi: 10.1002/ajmg.b.30967.

PMID:
19418498
20.

Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry.

Vogel CI, Greene B, Scherag A, Müller TD, Friedel S, Grallert H, Heid IM, Illig T, Wichmann HE, Schäfer H, Hebebrand J, Hinney A.

BMC Med Genet. 2009 Feb 19;10:14. doi: 10.1186/1471-2350-10-14.

21.

Exploring the genetic link between RLS and ADHD.

Schimmelmann BG, Friedel S, Nguyen TT, Sauer S, Ganz Vogel CI, Konrad K, Wilhelm C, Sinzig J, Renner TJ, Romanos M, Palmason H, Dempfle A, Walitza S, Freitag C, Meyer J, Linder M, Schäfer H, Warnke A, Lesch KP, Herpertz-Dahlman B, Hinney A, Hebebrand J.

J Psychiatr Res. 2009 Jul;43(10):941-5. doi: 10.1016/j.jpsychires.2009.01.003. Epub 2009 Feb 14.

PMID:
19223043
22.

Serotonin transporter gene polymorphism (5-HTTLPR), environmental conditions, and developing negative emotionality and fear in early childhood.

Pauli-Pott U, Friedel S, Hinney A, Hebebrand J.

J Neural Transm (Vienna). 2009 Apr;116(4):503-12. doi: 10.1007/s00702-008-0171-z. Epub 2009 Jan 10. Erratum in: J Neural Transm. 2009 Sep;116(9):1191. Friedl, Susann [corrected to Friedel, Susann].

PMID:
19137235
23.

Lifestyle intervention in obese children with variations in the melanocortin 4 receptor gene.

Reinehr T, Hebebrand J, Friedel S, Toschke AM, Brumm H, Biebermann H, Hinney A.

Obesity (Silver Spring). 2009 Feb;17(2):382-9. doi: 10.1038/oby.2008.422. Epub 2008 Nov 6.

24.

Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder.

Zhou K, Dempfle A, Arcos-Burgos M, Bakker SC, Banaschewski T, Biederman J, Buitelaar J, Castellanos FX, Doyle A, Ebstein RP, Ekholm J, Forabosco P, Franke B, Freitag C, Friedel S, Gill M, Hebebrand J, Hinney A, Jacob C, Lesch KP, Loo SK, Lopera F, McCracken JT, McGough JJ, Meyer J, Mick E, Miranda A, Muenke M, Mulas F, Nelson SF, Nguyen TT, Oades RD, Ogdie MN, Palacio JD, Pineda D, Reif A, Renner TJ, Roeyers H, Romanos M, Rothenberger A, Schäfer H, Sergeant J, Sinke RJ, Smalley SL, Sonuga-Barke E, Steinhausen HC, van der Meulen E, Walitza S, Warnke A, Lewis CM, Faraone SV, Asherson P.

Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1392-8. doi: 10.1002/ajmg.b.30878.

25.

Evidence for an influence of TCF7L2 polymorphism rs7903146 on insulin resistance and sensitivity indices in overweight children and adolescents during a lifestyle intervention.

Reinehr T, Friedel S, Mueller TD, Toschke AM, Hebebrand J, Hinney A.

Int J Obes (Lond). 2008 Oct;32(10):1521-4. doi: 10.1038/ijo.2008.146. Epub 2008 Sep 2.

PMID:
18762805
26.

Genetic aspects in attention-deficit/hyperactivity disorder.

Albayrak O, Friedel S, Schimmelmann BG, Hinney A, Hebebrand J.

J Neural Transm (Vienna). 2008;115(2):305-15. doi: 10.1007/s00702-007-0839-9. Epub 2008 Jan 16. Review.

PMID:
18200432
27.

Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants.

Hinney A, Nguyen TT, Scherag A, Friedel S, Brönner G, Müller TD, Grallert H, Illig T, Wichmann HE, Rief W, Schäfer H, Hebebrand J.

PLoS One. 2007 Dec 26;2(12):e1361.

28.

Gender-specific association of a functional coding polymorphism in the Neuropeptide S receptor gene with panic disorder but not with schizophrenia or attention-deficit/hyperactivity disorder.

Okamura N, Hashimoto K, Iyo M, Shimizu E, Dempfle A, Friedel S, Reinscheid RK.

Prog Neuropsychopharmacol Biol Psychiatry. 2007 Oct 1;31(7):1444-8. Epub 2007 Jul 3.

PMID:
17669576
29.

Association and linkage of allelic variants of the dopamine transporter gene in ADHD.

Friedel S, Saar K, Sauer S, Dempfle A, Walitza S, Renner T, Romanos M, Freitag C, Seitz C, Palmason H, Scherag A, Windemuth-Kieselbach C, Schimmelmann BG, Wewetzer C, Meyer J, Warnke A, Lesch KP, Reinhardt R, Herpertz-Dahlmann B, Linder M, Hinney A, Remschmidt H, Schäfer H, Konrad K, Hübner N, Hebebrand J.

Mol Psychiatry. 2007 Oct;12(10):923-33. Epub 2007 Apr 10.

PMID:
17579611
30.

Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13.

Friedel S, Reichwald K, Scherag A, Brumm H, Wermter AK, Fries HR, Koberwitz K, Wabitsch M, Meitinger T, Platzer M, Biebermann H, Hinney A, Hebebrand J.

BMC Genet. 2007 May 3;8:17.

31.

No evidence for an involvement of variants in the cannabinoid receptor gene (CNR1) in obesity in German children and adolescents.

Müller TD, Reichwald K, Wermter AK, Brönner G, Nguyen TT, Friedel S, Koberwitz K, Engeli S, Lichtner P, Meitinger T, Schäfer H, Hebebrand J, Hinney A.

Mol Genet Metab. 2007 Apr;90(4):429-34. Epub 2007 Feb 8.

PMID:
17292652
32.

No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHD.

Schimmelmann BG, Friedel S, Dempfle A, Warnke A, Lesch KP, Walitza S, Renner TJ, Romanos M, Herpertz-Dahlmann B, Linder M, Schäfer H, Seitz C, Palmason H, Freitag C, Meyer J, Konrad K, Hinney A, Hebebrand J.

J Neural Transm (Vienna). 2007;114(4):523-6. Epub 2007 Jan 15.

PMID:
17219016
33.

[Genetic findings in Attention-Deficit and Hyperactivity Disorder (ADHD)].

Schimmelmann BG, Friedel S, Christiansen H, Dempfle A, Hinney A, Hebebrand J.

Z Kinder Jugendpsychiatr Psychother. 2006 Nov;34(6):425-33. Review. German.

PMID:
17094061
34.

Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample.

Heiser P, Dempfle A, Friedel S, Konrad K, Hinney A, Kiefl H, Walitza S, Bettecken T, Saar K, Linder M, Warnke A, Herpertz-Dahlmann B, Schäfer H, Remschmidt H, Hebebrand J.

J Neural Transm (Vienna). 2007;114(4):513-21. Epub 2006 Nov 10.

PMID:
17093889
35.

Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studies.

Dempfle A, Wudy SA, Saar K, Hagemann S, Friedel S, Scherag A, Berthold LD, Alzen G, Gortner L, Blum WF, Hinney A, Nürnberg P, Schäfer H, Hebebrand J.

Hum Mol Genet. 2006 Sep 15;15(18):2772-83. Epub 2006 Aug 11.

PMID:
16905557
36.

Twin study on heritability of activity, attention, and impulsivity as assessed by objective measures.

Heiser P, Heinzel-Gutenbrunner M, Frey J, Smidt J, Grabarkiewicz J, Friedel S, Kühnau W, Schmidtke J, Remschmidt H, Hebebrand J.

J Atten Disord. 2006 May;9(4):575-81.

PMID:
16648224
37.

Case-control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa.

Cellini E, Nacmias B, Brecelj-Anderluh M, Badía-Casanovas A, Bellodi L, Boni C, Di Bella D, Estivill X, Fernandez-Aranda F, Foulon C, Friedel S, Gabrovsek M, Gorwood P, Gratacos M, Guelfi J, Hebebrand J, Hinney A, Holliday J, Hu X, Karwautz A, Kipman A, Komel R, Rotella CM, Ribases M, Ricca V, Romo L, Tomori M, Treasure J, Wagner G, Collier DA, Sorbi S; EC Framework V 'Factors in Healthy Eating' consortium.

Psychiatr Genet. 2006 Apr;16(2):51-2. No abstract available.

PMID:
16538179
38.

A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs.

Hebebrand J, Dempfle A, Saar K, Thiele H, Herpertz-Dahlmann B, Linder M, Kiefl H, Remschmidt H, Hemminger U, Warnke A, Knölker U, Heiser P, Friedel S, Hinney A, Schäfer H, Nürnberg P, Konrad K.

Mol Psychiatry. 2006 Feb;11(2):196-205.

PMID:
16222334
39.

Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder.

Walitza S, Renner TJ, Dempfle A, Konrad K, Wewetzer Ch, Halbach A, Herpertz-Dahlmann B, Remschmidt H, Smidt J, Linder M, Flierl L, Knölker U, Friedel S, Schäfer H, Gross C, Hebebrand J, Warnke A, Lesch KP.

Mol Psychiatry. 2005 Dec;10(12):1126-32.

PMID:
16116490
40.

Molecular genetic aspects of attention-deficit/hyperactivity disorder.

Heiser P, Friedel S, Dempfle A, Konrad K, Smidt J, Grabarkiewicz J, Herpertz-Dahlmann B, Remschmidt H, Hebebrand J.

Neurosci Biobehav Rev. 2004 Oct;28(6):625-41. Review.

PMID:
15527867
41.

Mutation screen of the brain derived neurotrophic factor gene (BDNF): identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention-deficit/hyperactivity disorder.

Friedel S, Horro FF, Wermter AK, Geller F, Dempfle A, Reichwald K, Smidt J, Brönner G, Konrad K, Herpertz-Dahlmann B, Warnke A, Hemminger U, Linder M, Kiefl H, Goldschmidt HP, Siegfried W, Remschmidt H, Hinney A, Hebebrand J.

Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):96-9.

PMID:
15457498
42.

Genetic risk factors in eating disorders.

Hinney A, Friedel S, Remschmidt H, Hebebrand J.

Am J Pharmacogenomics. 2004;4(4):209-23. Review.

PMID:
15287815
43.

Neuropathy due to hypovitaminosis following excessive weight loss.

Heiser P, Teepker M, Möller JC, Theisen FM, Friedel S, Hebebrand J, Remschmidt H.

J Am Acad Child Adolesc Psychiatry. 2004 Aug;43(8):928-9. No abstract available.

PMID:
15266188
44.

Ghrelin receptor gene: identification of several sequence variants in extremely obese children and adolescents, healthy normal-weight and underweight students, and children with short normal stature.

Wang HJ, Geller F, Dempfle A, Schäuble N, Friedel S, Lichtner P, Fontenla-Horro F, Wudy S, Hagemann S, Gortner L, Huse K, Remschmidt H, Bettecken T, Meitinger T, Schäfer H, Hebebrand J, Hinney A.

J Clin Endocrinol Metab. 2004 Jan;89(1):157-62.

PMID:
14715843
45.

Perspectives: molecular genetic research in human obesity.

Hebebrand J, Friedel S, Schäuble N, Geller F, Hinney A.

Obes Rev. 2003 Aug;4(3):139-46. Review.

PMID:
12916815
46.

Genome scan for childhood and adolescent obesity in German families.

Saar K, Geller F, Rüschendorf F, Reis A, Friedel S, Schäuble N, Nürnberg P, Siegfried W, Goldschmidt HP, Schäfer H, Ziegler A, Remschmidt H, Hinney A, Hebebrand J.

Pediatrics. 2003 Feb;111(2):321-7.

PMID:
12563058
47.

Glucose transporter 4 gene: association studies pertaining to alleles of two polymorphisms in extremely obese children and adolescents and in normal and underweight controls.

Friedel S, Antwerpen B, Hoch A, Vogel C, Grassl W, Geller F, Hebebrand J, Hinney A.

Ann N Y Acad Sci. 2002 Jun;967:554-7.

PMID:
12079888
48.

Green fluorescent proteins with short half-lives as reporters in Dictyostelium discoideum.

Deichsel H, Friedel S, Detterbeck A, Coyne C, Hamker U, MacWilliams HK.

Dev Genes Evol. 1999 Jan;209(1):63-8.

PMID:
9914420
49.

Trigger finger: the effect of partial release of the first annular pulley on triggering.

Topper SM, Jones DE, Klajnbart JO, Friedel SP.

Am J Orthop (Belle Mead NJ). 1997 Oct;26(10):675-7.

PMID:
9349888
50.

Ocular syphilis and neurosyphilis in a patient with human immunodeficiency virus infection.

Friedman RF, Ganiban GJ, Liss RA, Friedel SD.

Md Med J. 1995 Apr;44(4):284-8. Review.

PMID:
7731357

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