PUB - Publikationen an der Universität Bielefeld

What drives the allergic march?
Wahn U., Allergy 55(7), 2000
PMID: 10921457

The kaleidoscope of autoimmunity: multiple autoimmune syndromes and familial autoimmunity.
Anaya JM, Corena R, Castiblanco J, Rojas-Villarraga A, Shoenfeld Y., Expert Rev Clin Immunol 3(4), 2007
PMID: 20477166

Resolved and unresolved issues in the prevention and treatment of coronary artery disease: a workshop consensus statement.
Dzau V, Braunwald E., Am. Heart J. 121(4 Pt 1), 1991
PMID: 2008853

Genetic view on the phenomenon of combined diseases in man.
Puzyrev VP, Freidin MB., Acta Naturae 1(3), 2009
PMID: 22649614

The relationship between age of asthma onset and cardiovascular disease in Canadians.
Dogra S, Ardern CI, Baker J., J Asthma 44(10), 2007
PMID: 18097862

Asthma-like symptoms are increased in the metabolic syndrome.
Lee EJ, In KH, Ha ES, Lee KJ, Hur GY, Kang EH, Jung KH, Lee SY, Kim JH, Lee SY, Shin C, Shim JJ, Kang KH, Yoo SH., J Asthma 46(4), 2009
PMID: 19484665

Asthma, environmental risk factors, and hypertension among Arab Americans in metro Detroit.
Johnson M, Nriagu J, Hammad A, Savoie K, Jamil H., J Immigr Minor Health 12(5), 2008
PMID: 18998210

Sex-specific association between asthma and hypertension in nationally representative young Korean adults.
Lee HS, Park YM, Han K, Pekler G, Lee SS, Yoo S, Kim SR., Sci Rep 7(1), 2017
PMID: 29142269

Adult-onset asthma is associated with increased carotid atherosclerosis among women in the Atherosclerosis Risk in Communities (ARIC) study.
Onufrak S, Abramson J, Vaccarino V., Atherosclerosis 195(1), 2006
PMID: 17045272

Hypertension and Asthma: A Comorbid Relationship.
Christiansen SC, Schatz M, Yang SJ, Ngor E, Chen W, Zuraw BL., J Allergy Clin Immunol Pract 4(1), 2015
PMID: 26342745

Factors associated with systemic hypertension in asthma.
Ferguson S, Teodorescu MC, Gangnon RE, Peterson AG, Consens FB, Chervin RD, Teodorescu M., Lung 192(5), 2014
PMID: 24920421

Probing genetic overlap among complex human phenotypes.
Rzhetsky A, Wajngurt D, Park N, Zheng T., Proc. Natl. Acad. Sci. U.S.A. 104(28), 2007
PMID: 17609372

The human disease network.
Goh KI, Cusick ME, Valle D, Childs B, Vidal M, Barabasi AL., Proc. Natl. Acad. Sci. U.S.A. 104(21), 2007
PMID: 17502601

DeCoaD: determining correlations among diseases using protein interaction networks.
Hamaneh MB, Yu YK., BMC Res Notes 8(), 2015
PMID: 26047952

Novel candidate genes important for asthma and hypertension comorbidity revealed from associative gene networks.
Saik OV, Demenkov PS, Ivanisenko TV, Bragina EY, Freidin MB, Goncharova IA, Dosenko VE, Zolotareva OI, Hofestaedt R, Lavrik IN, Rogaev EI, Ivanisenko VA., BMC Med Genomics 11(Suppl 1), 2018
PMID: 29504915

HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants.
Ward LD, Kellis M., Nucleic Acids Res. 40(Database issue), 2011
PMID: 22064851

Systematic identification of trans eQTLs as putative drivers of known disease associations.
Westra HJ, Peters MJ, Esko T, Yaghootkar H, Schurmann C, Kettunen J, Christiansen MW, Fairfax BP, Schramm K, Powell JE, Zhernakova A, Zhernakova DV, Veldink JH, Van den Berg LH, Karjalainen J, Withoff S, Uitterlinden AG, Hofman A, Rivadeneira F, Hoen PAC', Reinmaa E, Fischer K, Nelis M, Milani L, Melzer D, Ferrucci L, Singleton AB, Hernandez DG, Nalls MA, Homuth G, Nauck M, Radke D, Volker U, Perola M, Salomaa V, Brody J, Suchy-Dicey A, Gharib SA, Enquobahrie DA, Lumley T, Montgomery GW, Makino S, Prokisch H, Herder C, Roden M, Grallert H, Meitinger T, Strauch K, Li Y, Jansen RC, Visscher PM, Knight JC, Psaty BM, Ripatti S, Teumer A, Frayling TM, Metspalu A, van Meurs JBJ, Franke L., Nat. Genet. 45(10), 2013
PMID: 24013639

Transcriptome and genome sequencing uncovers functional variation in humans.
Lappalainen T, Sammeth M, Friedlander MR, 't Hoen PA, Monlong J, Rivas MA, Gonzalez-Porta M, Kurbatova N, Griebel T, Ferreira PG, Barann M, Wieland T, Greger L, van Iterson M, Almlof J, Ribeca P, Pulyakhina I, Esser D, Giger T, Tikhonov A, Sultan M, Bertier G, MacArthur DG, Lek M, Lizano E, Buermans HP, Padioleau I, Schwarzmayr T, Karlberg O, Ongen H, Kilpinen H, Beltran S, Gut M, Kahlem K, Amstislavskiy V, Stegle O, Pirinen M, Montgomery SB, Donnelly P, McCarthy MI, Flicek P, Strom TM; Geuvadis Consortium, Lehrach H, Schreiber S, Sudbrak R, Carracedo A, Antonarakis SE, Hasler R, Syvanen AC, van Ommen GJ, Brazma A, Meitinger T, Rosenstiel P, Guigo R, Gut IG, Estivill X, Dermitzakis ET, Estivill X, Guigo R, Dermitzakis E, Antonarakis S, Meitinger T, Strom TM, Palotie A, Deleuze JF, Sudbrak R, Lerach H, Gut I, Syvanen AC, Gyllensten U, Schreiber S, Rosenstiel P, Brunner H, Veltman J, Hoen PA, van Ommen GJ, Carracedo A, Brazma A, Flicek P, Cambon-Thomsen A, Mangion J, Bentley D, Hamosh A., Nature 501(7468), 2013
PMID: 24037378

Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans.
GTEx Consortium, Ardlie KG, Deluca DS, Segre AV, Sullivan TJ, Young TR, Gelfand ET, Trowbridge CA, Maller JB, Tukiainen T, Lek M, Ward LD, Kheradpour P, Iriarte B, Meng Y, Palmer CD, Esko T, Winckler W, Hirschhorn JN, Kellis M, MacArthur DG, Getz G, Shabalin AA, Li G, Zhou YH, Nobel AB, Rusyn I, Wright FA, Lappalainen T, Ferreira PG, Ongen H, Rivas MA, Battle A, Mostafavi S, Monlong J, Sammeth M, Mele M, Reverter F, Goldmann JM, Koller D, Guigo R, McCarthy MI, Dermitzakis ET, Gamazon ER, Im HK, Konkashbaev A, Nicolae DL, Cox NJ, Flutre T, Wen X, Stephens M, Pritchard JK, Tu Z, Zhang B, Huang T, Long Q, Lin L, Yang J, Zhu J, Liu J, Brown A, Mestichelli B, Tidwell D, Lo E, Salvatore M, Shad S, Thomas JA, Lonsdale JT, Moser MT, Gillard BM, Karasik E, Ramsey K, Choi C, Foster BA, Syron J, Fleming J, Magazine H, Hasz R, Walters GD, Bridge JP, Miklos M, Sullivan S, Barker LK, Traino HM, Mosavel M, Siminoff LA, Valley DR, Rohrer DC, Jewell SD, Branton PA, Sobin LH, Barcus M, Qi L, McLean J, Hariharan P, Um KS, Wu S, Tabor D, Shive C, Smith AM, Buia SA, Undale AH, Robinson KL, Roche N, Valentino KM, Britton A, Burges R, Bradbury D, Hambright KW, Seleski J, Korzeniewski GE, Erickson K, Marcus Y, Tejada J, Taherian M, Lu C, Basile M, Mash DC, Volpi S, Struewing JP, Temple GF, Boyer J, Colantuoni D, Little R, Koester S, Carithers LJ, Moore HM, Guan P, Compton C, Sawyer SJ, Demchok JP, Vaught JB, Rabiner CA, Lockhart NC, Ardlie KG, Getz G, Wright FA, Kellis M, Volpi S, Dermitzakis ET., Science 348(6235), 2015
PMID: 25954001

Innate immune activation in neutrophilic asthma and bronchiectasis.
Simpson JL, Grissell TV, Douwes J, Scott RJ, Boyle MJ, Gibson PG., Thorax 62(3), 2006
PMID: 16844729

Toll-like receptors 2, 3 and 4 and thymic stromal lymphopoietin expression in fatal asthma.
Ferreira DS, Annoni R, Silva LF, Buttignol M, Santos AB, Medeiros MC, Andrade LN, Yick CY, Sterk PJ, Sampaio JL, Dolhnikoff M, Wenzel SE, Mauad T., Clin. Exp. Allergy 42(10), 2012
PMID: 22994343

Polymorphisms in toll-like receptor 4 gene are associated with asthma severity but not susceptibility in a Chinese Han population.
Zhang Q, Qian FH, Zhou LF, Wei GZ, Jin GF, Bai JL, Yin KS., J Investig Allergol Clin Immunol 21(5), 2011
PMID: 21905500

Association of Single Nucleotide Polymorphisms in Toll-like Receptor Genes With Asthma Risk: A Systematic Review and Meta-analysis.
Tizaoui K, Kaabachi W, Hamzaoui K, Hamzaoui A., Allergy Asthma Immunol Res 7(2), 2014
PMID: 25729620

The interaction between farming/rural environment and TLR2, TLR4, TLR6 and CD14 genetic polymorphisms in relation to early- and late-onset asthma.
Lau MY, Dharmage SC, Burgess JA, Win AK, Lowe AJ, Lodge C, Perret J, Hui J, Thomas PS, Morrison S, Giles GG, Hopper J, Abramson MJ, Walters EH, Matheson MC., Sci Rep 7(), 2017
PMID: 28262750

Suggestive evidence for genetic linkage between IgE phenotypes and chromosome 14q markers.
Mansur AH, Bishop DT, Markham AF, Morton NE, Holgate ST, Morrison JF., Am. J. Respir. Crit. Care Med. 159(6), 1999
PMID: 10351921

A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.
Ober C, Tsalenko A, Parry R, Cox NJ., Am. J. Hum. Genet. 67(5), 2000
PMID: 11022011

Chromosome 14 linkage analysis and mutation study of 2 serpin genes in allergic asthmatic families.
Malerba G, Patuzzo C, Trabetti E, Lauciello MC, Galavotti R, Pescollderungg L, Whalen MB, Zanoni G, Martinati LC, Boner AL, Pignatti PF., J. Allergy Clin. Immunol. 107(4), 2001
PMID: 11295654

Analysis of novel disease-related genes in bronchial asthma.
Yuyama N, Davies DE, Akaiwa M, Matsui K, Hamasaki Y, Suminami Y, Yoshida NL, Maeda M, Pandit A, Lordan JL, Kamogawa Y, Arima K, Nagumo F, Sugimachi M, Berger A, Richards I, Roberds SL, Yamashita T, Kishi F, Kato H, Arai K, Ohshima K, Tadano J, Hamasaki N, Miyatake S, Sugita Y, Holgate ST, Izuhara K., Cytokine 19(6), 2002
PMID: 12421571

Discovery and refinement of loci associated with lipid levels.
Willer CJ, Schmidt EM, Sengupta S, Peloso GM, Gustafsson S, Kanoni S, Ganna A, Chen J, Buchkovich ML, Mora S, Beckmann JS, Bragg-Gresham JL, Chang HY, Demirkan A, Den Hertog HM, Do R, Donnelly LA, Ehret GB, Esko T, Feitosa MF, Ferreira T, Fischer K, Fontanillas P, Fraser RM, Freitag DF, Gurdasani D, Heikkila K, Hypponen E, Isaacs A, Jackson AU, Johansson A, Johnson T, Kaakinen M, Kettunen J, Kleber ME, Li X, Luan J, Lyytikainen LP, Magnusson PKE, Mangino M, Mihailov E, Montasser ME, Muller-Nurasyid M, Nolte IM, O'Connell JR, Palmer CD, Perola M, Petersen AK, Sanna S, Saxena R, Service SK, Shah S, Shungin D, Sidore C, Song C, Strawbridge RJ, Surakka I, Tanaka T, Teslovich TM, Thorleifsson G, Van den Herik EG, Voight BF, Volcik KA, Waite LL, Wong A, Wu Y, Zhang W, Absher D, Asiki G, Barroso I, Been LF, Bolton JL, Bonnycastle LL, Brambilla P, Burnett MS, Cesana G, Dimitriou M, Doney ASF, Doring A, Elliott P, Epstein SE, Ingi Eyjolfsson G, Gigante B, Goodarzi MO, Grallert H, Gravito ML, Groves CJ, Hallmans G, Hartikainen AL, Hayward C, Hernandez D, Hicks AA, Holm H, Hung YJ, Illig T, Jones MR, Kaleebu P, Kastelein JJP, Khaw KT, Kim E, Klopp N, Komulainen P, Kumari M, Langenberg C, Lehtimaki T, Lin SY, Lindstrom J, Loos RJF, Mach F, McArdle WL, Meisinger C, Mitchell BD, Muller G, Nagaraja R, Narisu N, Nieminen TVM, Nsubuga RN, Olafsson I, Ong KK, Palotie A, Papamarkou T, Pomilla C, Pouta A, Rader DJ, Reilly MP, Ridker PM, Rivadeneira F, Rudan I, Ruokonen A, Samani N, Scharnagl H, Seeley J, Silander K, Stancakova A, Stirrups K, Swift AJ, Tiret L, Uitterlinden AG, van Pelt LJ, Vedantam S, Wainwright N, Wijmenga C, Wild SH, Willemsen G, Wilsgaard T, Wilson JF, Young EH, Zhao JH, Adair LS, Arveiler D, Assimes TL, Bandinelli S, Bennett F, Bochud M, Boehm BO, Boomsma DI, Borecki IB, Bornstein SR, Bovet P, Burnier M, Campbell H, Chakravarti A, Chambers JC, Chen YI, Collins FS, Cooper RS, Danesh J, Dedoussis G, de Faire U, Feranil AB, Ferrieres J, Ferrucci L, Freimer NB, Gieger C, Groop LC, Gudnason V, Gyllensten U, Hamsten A, Harris TB, Hingorani A, Hirschhorn JN, Hofman A, Hovingh GK, Hsiung CA, Humphries SE, Hunt SC, Hveem K, Iribarren C, Jarvelin MR, Jula A, Kahonen M, Kaprio J, Kesaniemi A, Kivimaki M, Kooner JS, Koudstaal PJ, Krauss RM, Kuh D, Kuusisto J, Kyvik KO, Laakso M, Lakka TA, Lind L, Lindgren CM, Martin NG, Marz W, McCarthy MI, McKenzie CA, Meneton P, Metspalu A, Moilanen L, Morris AD, Munroe PB, Njolstad I, Pedersen NL, Power C, Pramstaller PP, Price JF, Psaty BM, Quertermous T, Rauramaa R, Saleheen D, Salomaa V, Sanghera DK, Saramies J, Schwarz PEH, Sheu WH, Shuldiner AR, Siegbahn A, Spector TD, Stefansson K, Strachan DP, Tayo BO, Tremoli E, Tuomilehto J, Uusitupa M, van Duijn CM, Vollenweider P, Wallentin L, Wareham NJ, Whitfield JB, Wolffenbuttel BHR, Ordovas JM, Boerwinkle E, Palmer CNA, Thorsteinsdottir U, Chasman DI, Rotter JI, Franks PW, Ripatti S, Cupples LA, Sandhu MS, Rich SS, Boehnke M, Deloukas P, Kathiresan S, Mohlke KL, Ingelsson E, Abecasis GR; Global Lipids Genetics Consortium., Nat. Genet. 45(11), 2013
PMID: 24097068

Biological, clinical and population relevance of 95 loci for blood lipids.
Teslovich TM, Musunuru K, Smith AV, Edmondson AC, Stylianou IM, Koseki M, Pirruccello JP, Ripatti S, Chasman DI, Willer CJ, Johansen CT, Fouchier SW, Isaacs A, Peloso GM, Barbalic M, Ricketts SL, Bis JC, Aulchenko YS, Thorleifsson G, Feitosa MF, Chambers J, Orho-Melander M, Melander O, Johnson T, Li X, Guo X, Li M, Shin Cho Y, Jin Go M, Jin Kim Y, Lee JY, Park T, Kim K, Sim X, Twee-Hee Ong R, Croteau-Chonka DC, Lange LA, Smith JD, Song K, Hua Zhao J, Yuan X, Luan J, Lamina C, Ziegler A, Zhang W, Zee RY, Wright AF, Witteman JC, Wilson JF, Willemsen G, Wichmann HE, Whitfield JB, Waterworth DM, Wareham NJ, Waeber G, Vollenweider P, Voight BF, Vitart V, Uitterlinden AG, Uda M, Tuomilehto J, Thompson JR, Tanaka T, Surakka I, Stringham HM, Spector TD, Soranzo N, Smit JH, Sinisalo J, Silander K, Sijbrands EJ, Scuteri A, Scott J, Schlessinger D, Sanna S, Salomaa V, Saharinen J, Sabatti C, Ruokonen A, Rudan I, Rose LM, Roberts R, Rieder M, Psaty BM, Pramstaller PP, Pichler I, Perola M, Penninx BW, Pedersen NL, Pattaro C, Parker AN, Pare G, Oostra BA, O'Donnell CJ, Nieminen MS, Nickerson DA, Montgomery GW, Meitinger T, McPherson R, McCarthy MI, McArdle W, Masson D, Martin NG, Marroni F, Mangino M, Magnusson PK, Lucas G, Luben R, Loos RJ, Lokki ML, Lettre G, Langenberg C, Launer LJ, Lakatta EG, Laaksonen R, Kyvik KO, Kronenberg F, Konig IR, Khaw KT, Kaprio J, Kaplan LM, Johansson A, Jarvelin MR, Janssens AC, Ingelsson E, Igl W, Kees Hovingh G, Hottenga JJ, Hofman A, Hicks AA, Hengstenberg C, Heid IM, Hayward C, Havulinna AS, Hastie ND, Harris TB, Haritunians T, Hall AS, Gyllensten U, Guiducci C, Groop LC, Gonzalez E, Gieger C, Freimer NB, Ferrucci L, Erdmann J, Elliott P, Ejebe KG, Doring A, Dominiczak AF, Demissie S, Deloukas P, de Geus EJ, de Faire U, Crawford G, Collins FS, Chen YD, Caulfield MJ, Campbell H, Burtt NP, Bonnycastle LL, Boomsma DI, Boekholdt SM, Bergman RN, Barroso I, Bandinelli S, Ballantyne CM, Assimes TL, Quertermous T, Altshuler D, Seielstad M, Wong TY, Tai ES, Feranil AB, Kuzawa CW, Adair LS, Taylor HA Jr, Borecki IB, Gabriel SB, Wilson JG, Holm H, Thorsteinsdottir U, Gudnason V, Krauss RM, Mohlke KL, Ordovas JM, Munroe PB, Kooner JS, Tall AR, Hegele RA, Kastelein JJ, Schadt EE, Rotter JI, Boerwinkle E, Strachan DP, Mooser V, Stefansson K, Reilly MP, Samani NJ, Schunkert H, Cupples LA, Sandhu MS, Ridker PM, Rader DJ, van Duijn CM, Peltonen L, Abecasis GR, Boehnke M, Kathiresan S., Nature 466(7307), 2010
PMID: 20686565

Genetic studies of body mass index yield new insights for obesity biology.
o, Nature 518(7538), 2015
PMID: 25673413

Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Dichgans M, Malik R, Konig IR, Rosand J, Clarke R, Gretarsdottir S, Thorleifsson G, Mitchell BD, Assimes TL, Levi C, O'Donnell CJ, Fornage M, Thorsteinsdottir U, Psaty BM, Hengstenberg C, Seshadri S, Erdmann J, Bis JC, Peters A, Boncoraglio GB, Marz W, Meschia JF, Kathiresan S, Ikram MA, McPherson R, Stefansson K, Sudlow C, Reilly MP, Thompson JR, Sharma P, Hopewell JC, Chambers JC, Watkins H, Rothwell PM, Roberts R, Markus HS, Samani NJ, Farrall M, Schunkert H; METASTROKE Consortium; CARDIoGRAM Consortium; C4D Consortium; International Stroke Genetics Consortium, Gschwendtner A, Bevan S, Chen YC, DeStefano AL, Parati EA, Quertermous T, Ziegler A, Boerwinkle E, Holm H, Fischer M, Kessler T, Willenborg C, Laaksonen R, Voight BF, Stewart AF, Rader DJ, Hall AS, Kooner JS., Stroke 45(1), 2013
PMID: 24262325

A meta-analysis of gene expression signatures of blood pressure and hypertension.
Huan T, Esko T, Peters MJ, Pilling LC, Schramm K, Schurmann C, Chen BH, Liu C, Joehanes R, Johnson AD, Yao C, Ying SX, Courchesne P, Milani L, Raghavachari N, Wang R, Liu P, Reinmaa E, Dehghan A, Hofman A, Uitterlinden AG, Hernandez DG, Bandinelli S, Singleton A, Melzer D, Metspalu A, Carstensen M, Grallert H, Herder C, Meitinger T, Peters A, Roden M, Waldenberger M, Dorr M, Felix SB, Zeller T; International Consortium for Blood Pressure GWAS (ICBP), Vasan R, O'Donnell CJ, Munson PJ, Yang X, Prokisch H, Volker U, van Meurs JB, Ferrucci L, Levy D., PLoS Genet. 11(3), 2015
PMID: 25785607

Proficiency of data interpretation: identification of signaling SNPs/specific loci for coronary artery disease.
Cheema AN, Rosenthal SL, Ilyas Kamboh M., Database (Oxford) 2017(), 2017
PMID: 29220472

Inflammatory caspases: linking an intracellular innate immune system to autoinflammatory diseases.
Martinon F, Tschopp J., Cell 117(5), 2004
PMID: 15163405

Interleukin-1β is crucial for the induction of coronary artery inflammation in a mouse model of Kawasaki disease.
Lee Y, Schulte DJ, Shimada K, Chen S, Crother TR, Chiba N, Fishbein MC, Lehman TJ, Arditi M., Circulation 125(12), 2012
PMID: 22361326

Ribonuclease 4 protects neuron degeneration by promoting angiogenesis, neurogenesis, and neuronal survival under stress.
Li S, Sheng J, Hu JK, Yu W, Kishikawa H, Hu MG, Shima K, Wu D, Xu Z, Xin W, Sims KB, Landers JE, Brown RH Jr, Hu GF., Angiogenesis 16(2), 2012
PMID: 23143660

Angiogenin: a review of the pathophysiology and potential clinical applications.
Tello-Montoliu A, Patel JV, Lip GY., J. Thromb. Haemost. 4(9), 2006
PMID: 16961595

Arterial Hypertension Is Characterized by Imbalance of Pro-Angiogenic versus Anti-Angiogenic Factors.
Marek-Trzonkowska N, Kwieczynska A, Reiwer-Gostomska M, Kolinski T, Molisz A, Siebert J., PLoS ONE 10(5), 2015
PMID: 25951297

Vascular remodelling and angiogenesis in asthma: morphological aspects and pharmacological modulation.
Chetta A, Zanini A, Torre O, Olivieri D., Inflamm Allergy Drug Targets 6(1), 2007
PMID: 17352687

A comparative study of two angiogenic factors: vascular endothelial growth factor and angiogenin in induced sputum from asthmatic children in acute attack.
Abdel-Rahman AM, el-Sahrigy SA, Bakr SI., Chest 129(2), 2006
PMID: 16478840

Polymorphisms in the promoter region of catalase gene and essential hypertension.
Zhou XF, Cui J, DeStefano AL, Chazaro I, Farrer LA, Manolis AJ, Gavras H, Baldwin CT., Dis. Markers 21(1), 2005
PMID: 15735318

Catalase polymorphisms and metabolic diseases.
Hebert-Schuster M, Fabre EE, Nivet-Antoine V., Curr Opin Clin Nutr Metab Care 15(4), 2012
PMID: 22617568

Tobacco smoking, fruit and vegetable intake modify association between -21A>T polymorphism of catalase gene and risk of bronchial asthma.
Polonikov AV, Ivanov VP, Solodilova MA, Kozhuhov MA, Panfilov VI., J Asthma 46(3), 2009
PMID: 19373626

Human catalase, its polymorphisms, regulation and changes of its activity in different diseases.
Kodydkova J, Vavrova L, Kocik M, Zak A., Folia Biol. (Praha) 60(4), 2014
PMID: 25152049

Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression.
Zhou H, Polimanti R, Yang BZ, Wang Q, Han S, Sherva R, Nunez YZ, Zhao H, Farrer LA, Kranzler HR, Gelernter J., JAMA Psychiatry 74(12), 2017
PMID: 29071344

Genome-wide association study of comorbid depressive syndrome and alcohol dependence.
Edwards AC, Aliev F, Bierut LJ, Bucholz KK, Edenberg H, Hesselbrock V, Kramer J, Kuperman S, Nurnberger JI Jr, Schuckit MA, Porjesz B, Dick DM., Psychiatr. Genet. 22(1), 2012
PMID: 22064162