Labor Ι Publikationen

2013

Effects on transcriptional regulation and lipid droplet characteristics in the liver of female juvenile pigs after early postnatal feed restriction and refeeding are dependent on birth weight.
Nebendahl C1, Krüger R, Görs S, Albrecht E, Martens K, Hennig S, Storm N, Höppner W, Pfuhl R, Metzler-Zebeli BU, Hammon HM, Metges CC.
PLoS One. 2013 Nov 19;8(11)

The association of genetic markers for type 2 diabetes with prediabetic status - cross-sectional data of a diabetes prevention trial.
Zyriax BC, Salazar R, Hoeppner W, Vettorazzi E, Herder C, Windler E.
PLoS One. 2013 Sep 30;8(9)

Molecular epidemiology of multiple endocrine neoplasia 2: implications for RET screening in the new millenium.
Machens A, Lorenz K, Sekulla C, Höppner W, Frank-Raue K, Raue F, Dralle H.
Eur J Endocrinol. 2013 Feb 15;168(3)

 

2012

Apolipoprotein E genotype affects tissue metallothionein levels: studies in targeted gene replacement mice.
Graeser AC, Huebbe P, Storm N, Höppner W, Döring F, Wagner AE, Rimbach G.
Genes Nutr. 2012 Apr;7(2):247-55

2011

Hautalterung - warum der Schein oftmals trügt.
Salazar R, Höppner W
OM & Ernährung. 2011, 137

2010

Sequence Analysis of CYP21A1P in a German Population to Aid in the Molecular Biological Diagnosis of Congenital Adrenal Hyperplasia
Cumhur Cantürk, Ulrike Baade, Niels Storm, Ralf Pörtner, Wolfgang Höppner

Association analysis between gene variants of the tyrosine hydroxylase and the serotonin transporter in borderline personality disorder.
Tadić A, Elsässer A, Storm N, Baade U, Wagner S, Başkaya O, Lieb K, Dahmen N.
World J Biol Psychiatry. 2010 Feb;11(1):45-58

Selective deficiency of Gsalpha and the possible role of alternative gene products of GNAS in Albright hereditary osteodystrophy and pseudohypoparathyroidism type Ia.
Thiele S, Werner R, Ahrens W, Hübner A, Hinkel KG, Höppner W, Igl B, Hiort O.
Exp Clin Endocrinol Diabetes. 2010 Feb;118(2):127-32.

Polymorphisms in genes of the steroid receptor superfamily modify postmenopausal breast cancer risk associated with menopausal hormone therapy.
MARIE-GENICA Consortium on Genetic Susceptibility for Menopausal Hormone Therapy Related Breast Cancer Risk. Salazar R.
Int J Cancer. 2010 Jun 15;126(12):2935-46.

2009

Association analysis of serotonin receptor 1B (HTR1B) and brain-derived neurotrophic factor gene polymorphisms in Borderline personality disorder.
Tadić A, Elsässer A, Victor A, von Cube R, Başkaya O, Wagner S, Lieb K, Höppner W, Dahmen N.
J Neural Transm. 2009 Sep;116(9):1185-8.

Interaction between gene variants of the serotonin transporter promoter region (5-HTTLPR) and catechol O-methyltransferase (COMT) in borderline personality disorder.
Tadić A, Victor A, Başkaya O, von Cube R, Hoch J, Kouti I, Anicker NJ, Höppner W, Lieb K, Dahmen N.

Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 5;150B(4):487-95.

Genetik des oxidativen Stresses
Salazar R, Höppner W.
OM&Ernährung, 2009; 129

 

2008

Association analysis of SCN9A gene variants with borderline personality disorder.
Tadić A, Baskaya O, Victor A, Lieb K, Höppner W, Dahmen N.
J Psychiatr Res. 2008 Dec;43(2):155-63.

Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics.
Slanger T, Flesch-Janys D, Mutschelknauss E, Salazar R, Wang-Gohrke S, et al.
PLoS Genet. 2008 Apr 25;4(4):e1000054.

Association of a common AKAP9 variant with breast cancer risk: a collaborative analysis.
Bartram CR, Flesch-Janys D, Mutschelknauss E, Ashton K, Salazar R, Webb E, Hamann U, et al.
J Natl Cancer Inst. 2008 Mar 19;100(6):437-42. Epub 2008 Mar 11

 

2007

Developing effective screening strategies in multiple endocrine neoplasia type 1 (MEN 1) on the basis of clinical and sequencing data of German patients with MEN.
Schaaf L, Pickel J, Zinner K, Hering U, Höfler M, Goretzki PE, Spelsberg F, Raue F, von zur Mühlen A, Gerl H, Hensen J, Bartsch DK, Rothmund M, Schneyer U, Dralle H, Engelbach M, Karges W, Stalla GK, Höppner W.
Exp Clin Endocrinol Diabetes. 2007 Sep;115(8):509-17.

Gene-gene interaction associated with neural reward sensitivity.
Yacubian J, Sommer T, Schroeder K, Gläscher J, Kalisch R, Leuenberger B, Braus DF, Büchel C.
Proc Natl Acad Sci U S A. 2007 May 8;104(19):8125-30.

Mutations in the RET proto-oncogene in medullary thyroid carcinoma.
Höppner W.
Clin Lab. 2007;53(5-6):283-4.

Genpolymorphismen und Geschlecht
R. Salazar, W. Höppner
Blickpunkt DER MANN 2007; 5 (2): 00-00.

 

2006

Long-term outcome in 46 gene carriers of hereditary medullary thyroid carcinoma after prophylactic thyroidectomy: impact of individual RET genotype.
Frank-Raue K, Buhr H, Dralle H, Klar E, Senninger N, Weber T, Rondot S, Höppner W, Raue F.
Eur J Endocrinol. 2006 Aug;155(2):229-36.

Characteristic genomic imbalances in pediatric pheochromocytoma.
Hering A, Guratowska M, Bucsky P, Claussen U, Decker J, Ernst G, Hoeppner W, Michel S, Neumann H, Parlowsky T, Loncarevic I.
Genes Chromosomes Cancer. 2006 Jun;45(6):602-7.

Detection and genotyping of SHV beta-lactamase variants by mass spectrometry after base-specific cleavage of in vitro-generated RNA transcripts.
Stürenburg E, Storm N, Sobottka I, Horstkotte MA, Scherpe S, Aepfelbacher M, Müller S.
J Clin Microbiol. 2006 Mar;44(3):909-15.

Comparison of a new MALDI-TOF based resequencing method with Sanger sequencing for molecular diagnostics of multiple endocrine neoplasia type 2 (MEN2).
Storm, N., Vater, N., Salazar, R., Leuenberger, B., van den Boom, D., and Höppner, W.
Medgen  2006 18(1), 43.

 

2005

Coincidence of multiple endocrine neoplasia types 1 and 2: mutations in the RET protooncogene and MEN1 tumor suppressor gene in a family presenting with recurrent primary hyperparathyroidism.
Frank-Raue K, Rondot S, Hoeppner W, Goretzki P, Raue F, Meng W.
J Clin Endocrinol Metab. 2005 Jul;90(7):4063-7. Epub 2005 May 3. Erratum in: J Clin Endocrinol Metab. 2005 Oct;90(10):5575.

 

2004

Severe form of thyroid hormone resistance in a patient with homozygous/hemizygous mutation of T3 receptor gene.
Frank-Raue K, Lorenz A, Haag C, Höppner W, Boll HU, Knorr D, Hentze S, Raue F.
Eur J Endocrinol. 2004 Jun;150(6):819-23.

 

2000

Quality assurance in RT-PCR-based BCR/ABL diagnosis - results of an interlaboratory test and a standardization approach.

Burmeister T1, Maurer J, Aivado M, Elmaagacli AH, Grünebach F, Held KR, Hess G, Hochhaus A, Höppner W, Lentes KU, Lübbert M, Schäfer KL, Schafhausen P, Schmidt CA, Schüler F, Seeger K, Seelig R, Thiede C, Viehmann S, Weber C, Wilhelm S, Christmann A, Clement JH, Ebener U, Enczmann J, Leo R, Schleuning M, Schoch R, Thiel E.
Leukemia. 2000 Oct;14(10):1850-6.