3	A novel mitofusin 2 mutation causes canine fetal-onset neuroaxonal dystrophy.	Fyfe JC, Al-Tamimi RA, Liu J, Schäffer AA, Agarwala R, Henthorn PS.	21643798	PMC3165057	2011	10.1007/s10048-011-0285-6	\N
4	The insulin-like growth factor 1 receptor (IGF1R) contributes to reduced size in dogs.	Hoopes BC, Rimbault M, Liebers D, Ostrander EA, Sutter NB.	22903739	PMC3511640	2012	10.1007/s00335-012-9417-z	\N
5	Quantitative trait loci (QTL) study identifies novel genomic regions associated to Chiari-like malformation in Griffon Bruxellois dogs.	Lemay P, Knowler SP, Bouasker S, Nédélec Y, Platt S, Freeman C, Child G, Barreiro LB, Rouleau GA, Rusbridge C, Kibar Z.	24740420	PMC3989173	2014	10.1371/journal.pone.0089816	\N
6	Breed relationships facilitate fine-mapping studies: a 7.8-kb deletion cosegregates with Collie eye anomaly across multiple dog breeds.	Parker HG, Kukekova AV, Akey DT, Goldstein O, Kirkness EF, Baysac KC, Mosher DS, Aguirre GD, Acland GM, Ostrander EA.	17916641	PMC2045139	2007	10.1101/gr.6772807	\N
7	Single nucleotide polymorphisms (SNPs) in coding regions of canine dopamine- and serotonin-related genes.	Vĺge J, Lingaas F.	18226236	PMC2268707	2008	10.1186/1471-2156-9-10	\N
9	Genome-wide association analysis of canine atopic dermatitis and identification of disease related SNPs.	Wood SH, Ke X, Nuttall T, McEwan N, Ollier WE, Carter SD.	19838693	\N	2009	10.1007/s00251-009-0402-y	\N
15	PTPN22 polymorphisms may indicate a role for this gene in atopic dermatitis in West Highland white terriers.	Roque JB, O'Leary CA, Kyaw-Tanner M, Duffy DL, Gharahkhani P, Vogelnest L, Mason K, Shipstone M.	22208456	PMC3271996	2011	10.1186/1756-0500-4-571	\N
16	Assessment of canine BEST1 variations identifies new mutations and establishes an independent bestrophinopathy model (cmr3).	Zangerl B, Wickström K, Slavik J, Lindauer SJ, Ahonen S, Schelling C, Lohi H, Guziewicz KE, Aguirre GD.	21197113	PMC3008713	2010	\N	\N
22	An association study of 20 candidate genes with cryptorchidism in Siberian Husky dogs.	Zhao X, Du ZQ, Rothschild MF.	20646120	\N	2010	10.1111/j.1439-0388.2010.00859.x	\N
23	A non-synonymous mutation in the canine Pkd1 gene is associated with autosomal dominant polycystic kidney disease in Bull Terriers.	Gharahkhani P, O'Leary CA, Kyaw-Tanner M, Sturm RA, Duffy DL.	21818326	PMC3144903	2011	10.1371/journal.pone.0022455	\N
25	A novel locus for dilated cardiomyopathy maps to canine chromosome 8.	Werner P, Raducha MG, Prociuk U, Sleeper MM, Van Winkle TJ, Henthorn PS.	18442891	PMC2486407	2008	10.1016/j.ygeno.2008.03.007	\N
27	Canine Brachycephaly Is Associated with a Retrotransposon-Mediated Missplicing of SMOC2.	Marchant TW, Johnson EJ, McTeir L, Johnson CI, Gow A, Liuti T, Kuehn D, Svenson K, Bermingham ML, Drögemüller M, Nussbaumer M, Davey MG, Argyle DJ, Powell RM, Guilherme S, Lang J, Ter Haar G, Leeb T, Schwarz T, Mellanby RJ, Clements DN, Schoenebeck JJ.	28552356	PMC5462623	2017	\N	\N
28	Analysis of large versus small dogs reveals three genes on the canine X chromosome associated with body weight, muscling and back fat thickness.	Plassais J, Rimbault M, Williams FJ, Davis BW, Schoenebeck JJ, Ostrander EA.	28257443	PMC5357063	2017	\N	\N
29	Polymorphisms in canine platelet glycoproteins identify potential platelet antigens.	Callan MB, Werner P, Mason NJ, Meny GM, Raducha MG, Henthorn PS.	24209971	PMC3750671	2013	\N	\N
30	An ADAM9 mutation in canine cone-rod dystrophy 3 establishes homology with human cone-rod dystrophy 9.	Goldstein O, Mezey JG, Boyko AR, Gao C, Wang W, Bustamante CD, Anguish LJ, Jordan JA, Pearce-Kelling SE, Aguirre GD, Acland GM.	20806078	PMC2925905	2010	\N	\N
31	IQCB1 and PDE6B mutations cause similar early onset retinal degenerations in two closely related terrier dog breeds.	Goldstein O, Mezey JG, Schweitzer PA, Boyko AR, Gao C, Bustamante CD, Jordan JA, Aguirre GD, Acland GM.	24045995	PMC3809947	2013	\N	\N
32	Dogs and humans share a common susceptibility gene SRBD1 for glaucoma risk.	Kanemaki N, Tchedre KT, Imayasu M, Kawarai S, Sakaguchi M, Yoshino A, Itoh N, Meguro A, Mizuki N.	24040232	PMC3770690	2013	\N	\N
33	Single nucleotide polymorphisms and microsatellites in the canine glutathione S-transferase pi 1 (GSTP1) gene promoter.	Sacco J, Mann S, Toral K.	29046813	PMC5635497	2017	\N	\N
34	The ESR1 gene is associated with risk for canine mammary tumours.	Borge KS, Melin M, Rivera P, Thoresen SI, Webster MT, von Euler H, Lindblad-Toh K, Lingaas F.	23574728	PMC3637093	2013	\N	\N
36	Gaze-Following and Reaction to an Aversive Social Interaction Have Corresponding Associations with Variation in the OXTR Gene in Dogs but Not in Human Infants.	Oláh K, Topál J, Kovács K, Kis A, Koller D, Young Park S, Virányi Z.	29312041	PMC5732940	2017	\N	\N
37	An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs.	Ekenstedt KJ, Becker D, Minor KM, Shelton GD, Patterson EE, Bley T, Oevermann A, Bilzer T, Leeb T, Drögemüller C, Mickelson JR.	25275565	PMC4183422	2014	\N	\N
38	Variant detection and runs of homozygosity in next generation sequencing data elucidate the genetic background of Lundehund syndrome.	Metzger J, Pfahler S, Distl O.	27485430	PMC4971756	2016	\N	\N
39	Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogs.	Akkad DA, Gerding WM, Gasser RB, Epplen JT.	26401333	PMC4579392	2015	\N	\N
40	Assessment of Toll-like receptor 2, 4 and 9 SNP genotypes in canine sino-nasal aspergillosis.	Mercier E, Peters IR, Farnir F, Lavoué R, Day M, Clercx C, Peeters D.	25266752	PMC4143572	2014	\N	\N
41	A partial gene deletion of SLC45A2 causes oculocutaneous albinism in Doberman pinscher dogs.	Winkler PA, Gornik KR, Ramsey DT, Dubielzig RR, Venta PJ, Petersen-Jones SM, Bartoe JT.	24647637	PMC3960214	2014	\N	\N
42	Context and Individual Characteristics Modulate the Association between Oxytocin Receptor Gene Polymorphism and Social Behavior in Border Collies.	Turcsán B, Range F, Rónai Z, Koller D, Virányi Z.	29312078	PMC5742244	2017	\N	\N
43	Genome-wide association study to identify potential genetic modifiers in a canine model for Duchenne muscular dystrophy.	Brinkmeyer-Langford C, Balog-Alvarez C, Cai JJ, Davis BW, Kornegay JN.	27549615	PMC4994242	2016	\N	\N
44	Evaluation of the serotonergic genes htr1A, htr1B, htr2A, and slc6A4 in aggressive behavior of golden retriever dogs.	van den Berg L, Vos-Loohuis M, Schilder MB, van Oost BA, Hazewinkel HA, Wade CM, Karlsson EK, Lindblad-Toh K, Liinamo AE, Leegwater PA.	18066658	PMC2226021	2008	\N	\N
45	Assessment of coyote-wolf-dog admixture using ancestry-informative diagnostic SNPs.	Monzón J, Kays R, Dykhuizen DE.	24148003	PMC3899836	2014	\N	\N
46	Protein expression and genetic variability of canine Can f 1 in golden and Labrador retriever service dogs.	Breitenbuecher C, Belanger JM, Levy K, Mundell P, Fates V, Gershony L, Famula TR, Oberbauer AM.	27110374	PMC4840867	2016	\N	\N
47	A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis.	Abitbol M, Thibaud JL, Olby NJ, Hitte C, Puech JP, Maurer M, Pilot-Storck F, Hédan B, Dréano S, Brahimi S, Delattre D, André C, Gray F, Delisle F, Caillaud C, Bernex F, Panthier JJ, Aubin-Houzelstein G, Blot S, Tiret L.	20679209	PMC2930459	2010	\N	\N
48	Identification of novel genetic risk loci in Maltese dogs with necrotizing meningoencephalitis and evidence of a shared genetic risk across toy dog breeds.	Schrauwen I, Barber RM, Schatzberg SJ, Siniard AL, Corneveaux JJ, Porter BF, Vernau KM, Keesler RI, Matiasek K, Flegel T, Miller AD, Southard T, Mariani CL, Johnson GC, Huentelman MJ.	25393235	PMC4231098	2014	\N	\N
49	Saliva as an alternative source of high yield canine genomic DNA for genotyping studies.	Mitsouras K, Faulhaber EA.	19874604	PMC2781016	2009	\N	\N
50	XX Disorder of Sex Development is associated with an insertion on chromosome 9 and downregulation of RSPO1 in dogs (Canis lupus familiaris).	Meyers-Wallen VN, Boyko AR, Danko CG, Grenier JK, Mezey JG, Hayward JJ, Shannon LM, Gao C, Shafquat A, Rice EJ, Pujar S, Eggers S, Ohnesorg T, Sinclair AH.	29053721	PMC5650465	2017	\N	\N
51	Canine Leishmaniasis Progression is Associated with Vitamin D Deficiency.	Rodriguez-Cortes A, Martori C, Martinez-Florez A, Clop A, Amills M, Kubejko J, Llull J, Nadal JM, Alberola J.	28611427	PMC5469782	2017	\N	\N
52	Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 gene.	Gill JL, Capper D, Vanbellinghen JF, Chung SK, Higgins RJ, Rees MI, Shelton GD, Harvey RJ.	21420493	PMC4068303	2011	\N	\N
53	Searching for "monogenic diabetes" in dogs using a candidate gene approach.	Short AD, Holder A, Rothwell S, Massey J, Scholey R, Kennedy LJ, Catchpole B, Ollier WE.	26401325	PMC4579387	2014	\N	\N
54	Genome-Wide Scan for Visceral Leishmaniasis in Mixed-Breed Dogs Identifies Candidate Genes Involved in T Helper Cells and Macrophage Signaling.	Utsunomiya YT, Ribeiro ÉS, Quintal AP, Sangalli JR, Gazola VR, Paula HB, Trinconi CM, Lima VM, Perri SH, Taylor JF, Schnabel RD, Sonstegard TS, Garcia JF, Nunes CM.	26348501	PMC4562658	2015	\N	\N
55	Canine ?-defensin-1 (CBD1) gene as a possible marker for Leishmania infantum infection in dogs.	da Silva LG, Costa-Júnior CRL, Figueiredo-Júnior CAS, Leal-Balbino TC, Crovella S, Otranto D, Balbino VQ, Dantas-Torres F.	28427438	PMC5399410	2017	\N	\N
56	Oxytocin receptor gene polymorphisms are associated with human directed social behavior in dogs (Canis familiaris).	Kis A, Bence M, Lakatos G, Pergel E, Turcsán B, Pluijmakers J, Vas J, Elek Z, Brúder I, Földi L, Sasvári-Székely M, Miklósi A, Rónai Z, Kubinyi E.	24454713	PMC3893090	2014	\N	\N
57	Canine CNGA3 Gene Mutations Provide Novel Insights into Human Achromatopsia-Associated Channelopathies and Treatment.	Tanaka N, Dutrow EV, Miyadera K, Delemotte L, MacDermaid CM, Reinstein SL, Crumley WR, Dixon CJ, Casal ML, Klein ML, Aguirre GD, Tanaka JC, Guziewicz KE.	26407004	PMC4583268	2015	\N	\N
58	Polymorphisms in the canine monoamine oxidase a (MAOA) gene: identification and variation among five broad dog breed groups.	Sacco J, Ruplin A, Skonieczny P, Ohman M.	28101368	PMC5237129	2017	\N	\N
59	Multiple Genetic Associations with Irish Wolfhound Dilated Cardiomyopathy.	Simpson S, Dunning MD, Brownlie S, Patel J, Godden M, Cobb M, Mongan NP, Rutland CS.	28070514	PMC5187458	2016	\N	\N
60	Oxytocin and Opioid Receptor Gene Polymorphisms Associated with Greeting Behavior in Dogs.	Kubinyi E, Bence M, Koller D, Wan M, Pergel E, Ronai Z, Sasvari-Szekely M, Miklósi Á.	28936190	PMC5594098	2017	\N	\N
61	Familial cutaneous lupus erythematosus (CLE) in the German shorthaired pointer maps to CFA18, a canine orthologue to human CLE.	Wang P, Zangerl B, Werner P, Mauldin EA, Casal ML.	21132284	PMC3230530	2011	\N	\N
62	A large animal model for CNGB1 autosomal recessive retinitis pigmentosa.	Winkler PA, Ekenstedt KJ, Occelli LM, Frattaroli AV, Bartoe JT, Venta PJ, Petersen-Jones SM.	23977260	PMC3747135	2013	\N	\N
63	Non-synonymous genetic variation in exonic regions of canine Toll-like receptors.	Cuscó A, Sánchez A, Altet L, Ferrer L, Francino O.	26401328	PMC4579382	2014	\N	\N
64	Polymorphism and methylation of the MC4R gene in obese and non-obese dogs.	Mankowska M, Nowacka-Woszuk J, Graczyk A, Ciazynska P, Stachowiak M, Switonski M.	28755272	PMC5579139	2017	\N	\N
66	Gastric inhibitory polypeptide receptor: association analyses for obesity of several polymorphisms in large study groups.	Vogel CI, Scherag A, Brönner G, Nguyen TT, Wang HJ, Grallert H, Bornhorst A, Rosskopf D, Völzke H, Reinehr T, Rief W, Illig T, Wichmann HE, Schäfer H, Hebebrand J, Hinney A.	19254363	PMC2654891	2009	10.1186/1471-2350-10-19	PMC2654891
67	Chitinase-3-like 1 (CHI3L1) gene and schizophrenia: genetic association and a potential functional mechanism.	Yang MS, Morris DW, Donohoe G, Kenny E, O'Dushalaine CT, Schwaiger S, Nangle JM, Clarke S, Scully P, Quinn J, Meagher D, Baldwin P, Crumlish N, O'Callaghan E, Waddington JL, Gill M, Corvin A.	18281018	\N	2008	10.1016/j.biopsych.2007.12.012	ELSS0006322308000176
68	Clinical and genetic factors associated with lipoprotein-associated phospholipase A2 in the Framingham Heart Study.	Schnabel R, Dupuis J, Larson MG, Lunetta KL, Robins SJ, Zhu Y, Rong J, Yin X, Stirnadel HA, Nelson JJ, Wilson PW, Keaney JF, Vasan RS, Benjamin EJ.	19135199	PMC2893025	2009	10.1016/j.atherosclerosis.2008.10.030	ELSS0021915008007569
69	Polymorphisms in the CRP gene moderate an association between depressive symptoms and circulating levels of C-reactive protein.	Halder I, Marsland AL, Cheong J, Muldoon MF, Ferrell RE, Manuck SB.	19796676	PMC3074460	2010	10.1016/j.bbi.2009.09.014	ELSS0889159109004371
70	Association of adiponectin gene polymorphisms with type 2 diabetes in an African American population enriched for nephropathy.	Bostrom MA, Freedman BI, Langefeld CD, Liu L, Hicks PJ, Bowden DW.	19056609	PMC2628626	2009	10.2337/db08-0598	PMC2628626
71	Structure and sequence variation of the canine perforin gene.	Neta M, Wen X, Moore PF, Bienzle D.	19740553	\N	2010	10.1016/j.vetimm.2009.08.012	ELSS0165242709002839
73	SHARE: an adaptive algorithm to select the most informative set of SNPs for candidate genetic association.	Dai JY, Leblanc M, Smith NL, Psaty B, Kooperberg C.	19605740	PMC2742496	2009	10.1093/biostatistics/kxp023	PMC2742496
74	Genetics of attention deficit hyperactivity disorder.	Mick E, Faraone SV.	18295146	\N	2008	10.1016/j.chc.2007.11.011	ELSS1056499307001253
75	Pathogenic triad in COPD: oxidative stress, protease-antiprotease imbalance, and inflammation.	Fischer BM, Pavlisko E, Voynow JA.	21857781	PMC3157944	2011	10.2147/COPD.S10770	PMC3157944
77	Partial replication of a DRD4 association in ADHD individuals using a statistically derived quantitative trait for ADHD in a family-based association test.	Lasky-Su J, Banaschewski T, Buitelaar J, Franke B, Brookes K, Sonuga-Barke E, Ebstein R, Eisenberg J, Gill M, Manor I, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Taylor E, Zhou K, Thompson M, Asherson P, Faraone S	17560555	\N	2007	10.1016/j.biopsych.2007.03.006	ELSS0006322307002326
78	Assessment of genotype imputation methods.	Biernacka JM, Tang R, Li J, McDonnell SK, Rabe KG, Sinnwell JP, Rider DN, de Andrade M, Goode EL, Fridley BL.	20018042	PMC2795949	2009	\N	PMC2795949
80	A canine model of Cohen syndrome: Trapped Neutrophil Syndrome.	Shearman JR, Wilton AN.	21605373	PMC3128065	2011	10.1186/1471-2164-12-258	PMC3128065
82	Association analysis of chromosome 5 GABAA receptor cluster in Japanese schizophrenia patients.	Ikeda M, Iwata N, Suzuki T, Kitajima T, Yamanouchi Y, Kinoshita Y, Inada T, Ujike H, Ozaki N.	15993854	\N	2005	10.1016/j.biopsych.2005.05.002	ELSS0006322305005755
83	Complete sequencing of full-length canine ataxia telangiectasia mutated mRNA and characterization of its putative promoter.	Gentilini F, Turba ME, Forni M, Cinotti S.	19131117	\N	2009	10.1016/j.vetimm.2008.12.006	S0165242708007745
84	The Peru Urban versus Rural Asthma (PURA) Study: methods and baseline quality control data from a cross-sectional investigation into the prevalence, severity, genetics, immunology and environmental factors affecting asthma in adolescence in Peru.	Robinson CL, Baumann LM, Gilman RH, Romero K, Combe JM, Cabrera L, Hansel NN, Barnes K, Gonzalvez G, Wise RA, Breysse PN, Checkley W.	22357570	PMC3289983	2012	10.1136/bmjopen-2011-000421	PMC3289983
85	No effect of APOE and PVRL2 on the clinical outcome of multiple sclerosis.	Ramagopalan SV, Deluca GC, Morrison KM, Herrera BM, Dyment DA, Orton S, Bihoreau MT, Degenhardt A, Pugliatti M, Sadovnick AD, Sotgiu S, Ebers GC.	17376543	\N	2007	10.1016/j.jneuroim.2007.02.003	ELSS0165572807000616
88	Eotaxin-3 gene polymorphisms are associated with rheumatoid arthritis in a Korean population.	Chae SC, Park YR, Shim SC, Lee IK, Chung HT.	15784470	\N	2005	10.1016/j.humimm.2005.01.002	ELSS0198885905000030
89	A one base pair deletion in the canine ATP13A2 gene causes exon skipping and late-onset neuronal ceroid lipofuscinosis in the Tibetan terrier.	Wöhlke A, Philipp U, Bock P, Beineke A, Lichtner P, Meitinger T, Distl O.	22022275	PMC3192819	2011	10.1371/journal.pgen.1002304	PMC3192819
90	Hepatocyte growth factor and myopia: genetic association analyses in a Caucasian population.	Yanovitch T, Li YJ, Metlapally R, Abbott D, Viet KN, Young TL.	19471602	PMC2684748	2009	\N	PMC2684748
91	Candidate genetic analysis of plasma high-density lipoprotein-cholesterol and severity of coronary atherosclerosis.	Chen SN, Cilingiroglu M, Todd J, Lombardi R, Willerson JT, Gotto AM, Ballantyne CM, Marian AJ.	19878569	PMC2775733	2009	10.1186/1471-2350-10-111	PMC2775733
92	Analysis of the polymorphisms in eotaxin gene family and their association with asthma, IgE, and eosinophil.	Chae SC, Lee YC, Park YR, Shin JS, Song JH, Oh GJ, Hong ST, Pae HO, Choi BM, Chung HT.	15207712	\N	2004	10.1016/j.bbrc.2004.05.136	ELSS0006291X04011453
93	W1250 Genome-Wide Association Scan Reveals Polymorphisms in the P67phox Subunit (Ncf2) of the NADPH Oxidase Complex in Boxer Dogs With Adherent and Invasive E.Coli-Associated Granulomatous Colitis: A Potential Model of Chronic Granulomatous Disease	Craven, Melanie; Acland, Gregory M.; Mezey, Jason; Boyko, Adam; Wang, Wei; Meurs, Kathryn; McDonough, Sean; Simpson, Kenneth W.	\N	\N	2010	10.1016/S0016-5085(10)63141-1	ELSS0016508510631411
94	W1246 Disease Phenotype are Genetically-Influenced in British Twins With Inflammatory Bowel Disease	Ng, Siew C.; Woodrow, Susannah R.; Patel, Nisha; Subhani, Javaid; Harbord, Marcus	\N	\N	2010	10.1016/S0016-5085(10)63137-X	ELSS001650851063137X
95	W1251 Epigenetic Variation of Dnmt3l in Paediatric Ileal Crohn's Disease	Drini, Musa; Wong, Nicholas C.; Wagner, Josef; Craig, Jeffrey M.; Kirkwood, Carl D.; Catto-Smith, Anthony G.; Cameron, Don; Saffery, Richard; Macrae, Finlay A.	\N	\N	2010	10.1016/S0016-5085(10)63142-3	ELSS0016508510631423
96	W1248 Identification of a Single Nucleotide Polymorphism That Associates With Longitudinal Disease Behaviour in Crohn's Disease and May Have Prognostic Utility	Lee, James; Anderson, Carl A.; Wesley, Emma; Ahmad, Tariq; Edwards, Cathryn M.; Parkes, Miles; Smith, Kenneth G.	\N	\N	2010	10.1016/S0016-5085(10)63139-3	ELSS0016508510631393
97	W1247 Nkx2-3 Variant Rs11190140 is Associated With IBD and Alters NFAT Transcription Factor Binding	John, Gerrit; Lin, Zhenwu; Hegarty, John P.; Berg, Arthur; Pastor, Danielle M.; Kelly, Ashley A.; Wang, Yunhua; Poritz, Lisa S.; Koltun, Walter	\N	\N	2010	10.1016/S0016-5085(10)63138-1	ELSS0016508510631381
98	W1249 A Family-Based Study Provides Evidence for a Genetically Determined Intestinal Barrier Defect in Ulcerative Colitis	Büning, Carsten; Saupe, Nora; Baumgart, Daniel C.; Sturm, Andreas; Zeitz, Martin; Haas, Verena K.	\N	\N	2010	10.1016/S0016-5085(10)63140-X	ELSS001650851063140X
99	Despite identifying some shared gene associations with human atopic dermatitis the use of multiple dog breeds from various locations limits detection of gene associations in canine atopic dermatitis.	Wood SH, Ollier WE, Nuttall T, McEwan NA, Carter SD.	20728225	\N	2010	10.1016/j.vetimm.2010.07.020	ELSS0165242710002710