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1.

Maternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritance.

Esparza-Gordillo, Jorge; Matanovic, Anja; Marenholz, Ingo; Bauerfeind, Anja; Rohde, Klaus; Nemat, Katja; Lee-Kirsch, Min-Ae; Nordenskjöld, Magnus; Winge, Marten C G; Keil, Thomas; Krüger, Renate; Lau, Susanne; Beyer, Kirsten; Kalb, Birgit; Niggemann, Bodo; Hübner, Norbert; Cordell, Heather J; Bradley, Maria; Lee, Young-Ae.

PLoS Genet; 11(3): e1005076, 2015 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-25757221

2.

DNA methylation within melatonin receptor 1A (MTNR1A) mediates paternally transmitted genetic variant effect on asthma plus rhinitis.

Sarnowski, Chloé; Laprise, Catherine; Malerba, Giovanni; Moffatt, Miriam F; Dizier, Marie-Hélène; Morin, Andréanne; Vincent, Quentin B; Rohde, Klaus; Esparza-Gordillo, Jorge; Margaritte-Jeannin, Patricia; Liang, Liming; Lee, Young-Ae; Bousquet, Jean; Siroux, Valérie; Pignatti, Pier Franco; Cookson, William O; Lathrop, Mark; Pastinen, Tomi; Demenais, Florence; Bouzigon, Emmanuelle.

J Allergy Clin Immunol; 138(3): 748-753, 2016 09.

Artículo en Inglés | MEDLINE | ID: mdl-27038909

3.

Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus.

Lee-Kirsch, Min Ae; Gong, Maolian; Chowdhury, Dipanjan; Senenko, Lydia; Engel, Kerstin; Lee, Young-Ae; de Silva, Udesh; Bailey, Suzanna L; Witte, Torsten; Vyse, Timothy J; Kere, Juha; Pfeiffer, Christiane; Harvey, Scott; Wong, Andrew; Koskenmies, Sari; Hummel, Oliver; Rohde, Klaus; Schmidt, Reinhold E; Dominiczak, Anna F; Gahr, Manfred; Hollis, Thomas; Perrino, Fred W; Lieberman, Judy; Hübner, Norbert.

Nat Genet; 39(9): 1065-7, 2007 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-17660818

4.

A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis.

Witt, Heiko; Sahin-Tóth, Miklós; Landt, Olfert; Chen, Jian-Min; Kähne, Thilo; Drenth, Joost Ph; Kukor, Zoltán; Szepessy, Edit; Halangk, Walter; Dahm, Stefan; Rohde, Klaus; Schulz, Hans-Ulrich; Le Maréchal, Cédric; Akar, Nejat; Ammann, Rudolf W; Truninger, Kaspar; Bargetzi, Mario; Bhatia, Eesh; Castellani, Carlo; Cavestro, Giulia Martina; Cerny, Milos; Destro-Bisol, Giovanni; Spedini, Gabriella; Eiberg, Hans; Jansen, Jan B M J; Koudova, Monika; Rausova, Eva; Macek, Milan; Malats, Núria; Real, Francisco X; Menzel, Hans-Jürgen; Moral, Pedro; Galavotti, Roberta; Pignatti, Pier Franco; Rickards, Olga; Spicak, Julius; Zarnescu, Narcis Octavian; Böck, Wolfgang; Gress, Thomas M; Friess, Helmut; Ockenga, Johann; Schmidt, Hartmut; Pfützer, Roland; Löhr, Matthias; Simon, Peter; Weiss, Frank Ulrich; Lerch, Markus M; Teich, Niels; Keim, Volker; Berg, Thomas.

Nat Genet; 38(6): 668-73, 2006 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-16699518

5.

Multi-locus stepwise regression: a haplotype-based algorithm for finding genetic associations applied to atopic dermatitis.

Knüppel, Sven; Esparza-Gordillo, Jorge; Marenholz, Ingo; Holzhütter, Hermann-Georg; Bauerfeind, Anja; Ruether, Andreas; Weidinger, Stephan; Lee, Young-Ae; Rohde, Klaus.

BMC Med Genet; 13: 8, 2012 Jan 27.

Artículo en Inglés | MEDLINE | ID: mdl-22284537

6.

Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis.

Söderhäll, Cilla; Marenholz, Ingo; Kerscher, Tamara; Rüschendorf, Franz; Esparza-Gordillo, Jorge; Worm, Margitta; Gruber, Christoph; Mayr, Gabriele; Albrecht, Mario; Rohde, Klaus; Schulz, Herbert; Wahn, Ulrich; Hubner, Norbert; Lee, Young-Ae.

PLoS Biol; 5(9): e242, 2007 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-17850181

7.

An interaction between filaggrin mutations and early food sensitization improves the prediction of childhood asthma.

Marenholz, Ingo; Kerscher, Tamara; Bauerfeind, Anja; Esparza-Gordillo, Jorge; Nickel, Renate; Keil, Thomas; Lau, Susanne; Rohde, Klaus; Wahn, Ulrich; Lee, Young-Ae.

J Allergy Clin Immunol; 123(4): 911-6, 2009 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-19348926

8.

Association of the HLA region with multiple sclerosis as confirmed by a genome screen using >10,000 SNPs on DNA chips.

Gödde, René; Rohde, Klaus; Becker, Christian; Toliat, Mahammad R; Entz, Patricia; Suk, Anita; Müller, Norbert; Sindern, Eckhart; Haupts, Michael; Schimrigk, Sebastian; Nürnberg, Peter; Epplen, Jörg T.

J Mol Med (Berl); 83(6): 486-94, 2005 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-15770496

9.

Simulation of Rapoport's rule for latitudinal species spread.

Stauffer, Dietrich; Rohde, Klaus.

Theory Biosci; 125(1): 55-65, 2006 Aug.

Artículo en Inglés | MEDLINE | ID: mdl-17046373

10.

Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy.

Sander, Thomas; Toliat, Mohammad Reza; Heils, Armin; Leschik, Gundula; Becker, Christian; Rüschendorf, Franz; Rohde, Klaus; Mundlos, Stefan; Nürnberg, Peter.

Epilepsy Res; 51(3): 249-55, 2002 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-12399075

11.

Comparing the richness of metazoan ectoparasite communities of marine fishes: controlling for host phylogeny.

Poulin, Robert; Rohde, Klaus.

Oecologia; 110(2): 278-283, 1997 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-28307435

12.

Ecology and biogeography of marine parasites.

Rohde, Klaus.

Adv Mar Biol; 43: 1-86, 2002.

Artículo en Inglés | MEDLINE | ID: mdl-12154612

13.

Natural laws, vacant niches and superorganisms. A response to Woodley.

Rohde, Klaus.

Riv Biol; 101(3): 340-6, 2008.

Artículo en Inglés | MEDLINE | ID: mdl-19322755

14.

Vacant niches and the possible operation of natural laws in ecosystems.

Rohde, Klaus.

Riv Biol; 101(1): 13-28, 2008.

Artículo en Inglés | MEDLINE | ID: mdl-18816906

15.

Evaluation of 41 candidate gene variants for obesity in the EPIC-Potsdam cohort by multi-locus stepwise regression.

Knüppel, Sven; Rohde, Klaus; Meidtner, Karina; Drogan, Dagmar; Holzhütter, Hermann-Georg; Boeing, Heiner; Fisher, Eva.

PLoS One; 8(7): e68941, 2013.

Artículo en Inglés | MEDLINE | ID: mdl-23874820

16.

A common variant on chromosome 11q13 is associated with atopic dermatitis.

Esparza-Gordillo, Jorge; Weidinger, Stephan; Fölster-Holst, Regina; Bauerfeind, Anja; Ruschendorf, Franz; Patone, Giannino; Rohde, Klaus; Marenholz, Ingo; Schulz, Florian; Kerscher, Tamara; Hubner, Norbert; Wahn, Ulrich; Schreiber, Stefan; Franke, Andre; Vogler, Rainer; Heath, Simon; Baurecht, Hansjörg; Novak, Natalija; Rodriguez, Elke; Illig, Thomas; Lee-Kirsch, Min-Ae; Ciechanowicz, Andrzej; Kurek, Michael; Piskackova, Tereza; Macek, Milan; Lee, Young-Ae; Ruether, Andreas.

Nat Genet; 41(5): 596-601, 2009 May.

Artículo en Inglés | MEDLINE | ID: mdl-19349984

17.

Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease.

Monti, Jan; Fischer, Judith; Paskas, Svetlana; Heinig, Matthias; Schulz, Herbert; Gösele, Claudia; Heuser, Arnd; Fischer, Robert; Schmidt, Cosima; Schirdewan, Alexander; Gross, Volkmar; Hummel, Oliver; Maatz, Henrike; Patone, Giannino; Saar, Kathrin; Vingron, Martin; Weldon, Steven M; Lindpaintner, Klaus; Hammock, Bruce D; Rohde, Klaus; Dietz, Rainer; Cook, Stuart A; Schunck, Wolf-Hagen; Luft, Friedrich C; Hubner, Norbert.

Nat Genet; 40(5): 529-37, 2008 May.

Artículo en Inglés | MEDLINE | ID: mdl-18443590

18.

The effect of single-nucleotide polymorphism marker selection on patterns of haplotype blocks and haplotype frequency estimates.

Nothnagel, Michael; Rohde, Klaus.

Am J Hum Genet; 77(6): 988-98, 2005 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-16380910

19.

Quantitative trait locus analysis reveals two intragenic sites that influence O6-alkylguanine-DNA alkyltransferase activity in peripheral blood mononuclear cells.

Margison, Geoffrey P; Heighway, Jim; Pearson, Steven; McGown, Gail; Thorncroft, Mary R; Watson, Amanda J; Harrison, Kathryn L; Lewis, Sarah J; Rohde, Klaus; Barber, Philip V; O'Donnell, Paul; Povey, Andrew C; Santibáñez-Koref, Mauro F.

Carcinogenesis; 26(8): 1473-80, 2005 Aug.

Artículo en Inglés | MEDLINE | ID: mdl-15831531

20.

STAT6 as an asthma candidate gene: polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study.

Duetsch, Gabriele; Illig, Thomas; Loesgen, Sabine; Rohde, Klaus; Klopp, Norman; Herbon, Nicole; Gohlke, Henning; Altmueller, Janine; Wjst, Matthias.

Hum Mol Genet; 11(6): 613-21, 2002 Mar 15.

Artículo en Inglés | MEDLINE | ID: mdl-11912176

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Maternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritance.

DNA methylation within melatonin receptor 1A (MTNR1A) mediates paternally transmitted genetic variant effect on asthma plus rhinitis.

Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus.

A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis.

Multi-locus stepwise regression: a haplotype-based algorithm for finding genetic associations applied to atopic dermatitis.

Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis.

An interaction between filaggrin mutations and early food sensitization improves the prediction of childhood asthma.

Association of the HLA region with multiple sclerosis as confirmed by a genome screen using >10,000 SNPs on DNA chips.

Simulation of Rapoport's rule for latitudinal species spread.

Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy.

Comparing the richness of metazoan ectoparasite communities of marine fishes: controlling for host phylogeny.

Ecology and biogeography of marine parasites.

Natural laws, vacant niches and superorganisms. A response to Woodley.

Vacant niches and the possible operation of natural laws in ecosystems.

Evaluation of 41 candidate gene variants for obesity in the EPIC-Potsdam cohort by multi-locus stepwise regression.

A common variant on chromosome 11q13 is associated with atopic dermatitis.

Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease.

The effect of single-nucleotide polymorphism marker selection on patterns of haplotype blocks and haplotype frequency estimates.

Quantitative trait locus analysis reveals two intragenic sites that influence O6-alkylguanine-DNA alkyltransferase activity in peripheral blood mononuclear cells.

STAT6 as an asthma candidate gene: polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study.