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For: Schwarzenbacher H, Burgstaller J, Seefried FR, Wurmser C, Hilbe M, Jung S, Fuerst C, Dinhopl N, Weissenböck H, Fuerst-Waltl B, Dolezal M, Winkler R, Grueter O, Bleul U, Wittek T, Fries R, Pausch H. A missense mutation in TUBD1 is associated with high juvenile mortality in Braunvieh and Fleckvieh cattle. BMC Genomics 2016;17:400. [PMID: 27225349 DOI: 10.1186/s12864-016-2742-y] [Cited by in Crossref: 33] [Cited by in F6Publishing: 33] [Article Influence: 5.5] [Reference Citation Analysis]
Number Citing Articles
1 Hiltpold M, Janett F, Mapel XM, Kadri NK, Fang Z, Schwarzenbacher H, Seefried FR, Spengeler M, Witschi U, Pausch H. A 1-bp deletion in bovine QRICH2 causes low sperm count and immotile sperm with multiple morphological abnormalities. Genet Sel Evol 2022;54. [DOI: 10.1186/s12711-022-00710-0] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
2 Lim KS, Kim HC, Choi BH, Son JW, Lee KT, Choi TJ, Cho YM, Chai HH, Park JE, Park W, Lim C, Kim JM, Lim D. Identification of Monoallelically Expressed Genes Associated with Economic Traits in Hanwoo (Korean Native Cattle). Animals (Basel) 2021;12:84. [PMID: 35011190 DOI: 10.3390/ani12010084] [Reference Citation Analysis]
3 Häfliger IM, Seefried FR, Spengeler M, Drögemüller C. Mining massive genomic data of two Swiss Braunvieh cattle populations reveals six novel candidate variants that impair reproductive success. Genet Sel Evol 2021;53:95. [PMID: 34915862 DOI: 10.1186/s12711-021-00686-3] [Reference Citation Analysis]
4 Häfliger IM, Seefried FR, Drögemüller C. Reverse Genetic Screen for Deleterious Recessive Variants in the Local Simmental Cattle Population of Switzerland. Animals (Basel) 2021;11:3535. [PMID: 34944310 DOI: 10.3390/ani11123535] [Reference Citation Analysis]
5 Bengtsson C, Stålhammar H, Thomasen JR, Eriksson S, Fikse WF, Strandberg E. Mating allocations in Nordic Red Dairy Cattle using genomic information. J Dairy Sci 2021:S0022-0302(21)01021-3. [PMID: 34799119 DOI: 10.3168/jds.2021-20849] [Reference Citation Analysis]
6 Sledzieski S, Singh R, Cowen L, Berger B. D-SCRIPT translates genome to phenome with sequence-based, structure-aware, genome-scale predictions of protein-protein interactions. Cell Syst 2021;12:969-982.e6. [PMID: 34536380 DOI: 10.1016/j.cels.2021.08.010] [Cited by in Crossref: 1] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
7 Nosková A, Hiltpold M, Janett F, Echtermann T, Fang ZH, Sidler X, Selige C, Hofer A, Neuenschwander S, Pausch H. Infertility due to defective sperm flagella caused by an intronic deletion in DNAH17 that perturbs splicing. Genetics 2021;217:iyaa033. [PMID: 33724408 DOI: 10.1093/genetics/iyaa033] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
8 Ben Braiek M, Fabre S, Hozé C, Astruc JM, Moreno-Romieux C. Identification of homozygous haplotypes carrying putative recessive lethal mutations that compromise fertility traits in French Lacaune dairy sheep. Genet Sel Evol 2021;53:41. [PMID: 33932977 DOI: 10.1186/s12711-021-00634-1] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
9 Stathatos GG, Dunleavy JEM, Zenker J, O'Bryan MK. Delta and epsilon tubulin in mammalian development. Trends Cell Biol 2021;31:774-87. [PMID: 33867233 DOI: 10.1016/j.tcb.2021.03.010] [Reference Citation Analysis]
10 Sasaki S, Watanabe T, Ibi T, Hasegawa K, Sakamoto Y, Moriwaki S, Kurogi K, Ogino A, Yasumori T, Wakaguri H, Muraki E, Miki Y, Yoshida Y, Inoue Y, Tabuchi I, Iwao K, Arishima T, Kawashima K, Watanabe M, Sugano S, Sugimoto Y, Suzuki Y. Identification of deleterious recessive haplotypes and candidate deleterious recessive mutations in Japanese Black cattle. Sci Rep 2021;11:6687. [PMID: 33758295 DOI: 10.1038/s41598-021-86225-y] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
11 Hiltpold M, Niu G, Kadri NK, Crysnanto D, Fang ZH, Spengeler M, Schmitz-Hsu F, Fuerst C, Schwarzenbacher H, Seefried FR, Seehusen F, Witschi U, Schnieke A, Fries R, Bollwein H, Flisikowski K, Pausch H. Activation of cryptic splicing in bovine WDR19 is associated with reduced semen quality and male fertility. PLoS Genet 2020;16:e1008804. [PMID: 32407316 DOI: 10.1371/journal.pgen.1008804] [Cited by in Crossref: 6] [Cited by in F6Publishing: 12] [Article Influence: 3.0] [Reference Citation Analysis]
12 Wang Q, Zhang Q, Wang X, Zhang Y, Zhao X. Yak FOXO1 and FOXO3 SNPs and association with production traits, and their promotes cells apoptosis via RNAi. Gene 2020;743:144592. [PMID: 32198125 DOI: 10.1016/j.gene.2020.144592] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
13 Wu X, Mesbah-Uddin M, Guldbrandtsen B, Lund MS, Sahana G. Novel haplotypes responsible for prenatal death in Nordic Red and Danish Jersey cattle. J Dairy Sci 2020;103:4570-8. [PMID: 32197842 DOI: 10.3168/jds.2019-17831] [Cited by in Crossref: 3] [Cited by in F6Publishing: 7] [Article Influence: 1.5] [Reference Citation Analysis]
14 Wu X, Mesbah-Uddin M, Guldbrandtsen B, Lund MS, Sahana G. Haplotypes responsible for early embryonic lethality detected in Nordic Holsteins. J Dairy Sci 2019;102:11116-23. [PMID: 31548059 DOI: 10.3168/jds.2019-16651] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
15 Jagannathan V, Drögemüller C, Leeb T; Dog Biomedical Variant Database Consortium (DBVDC). A comprehensive biomedical variant catalogue based on whole genome sequences of 582 dogs and eight wolves. Anim Genet 2019;50:695-704. [PMID: 31486122 DOI: 10.1111/age.12834] [Cited by in Crossref: 56] [Cited by in F6Publishing: 53] [Article Influence: 18.7] [Reference Citation Analysis]
16 Fang ZH, Pausch H. Multi-trait meta-analyses reveal 25 quantitative trait loci for economically important traits in Brown Swiss cattle. BMC Genomics 2019;20:695. [PMID: 31481029 DOI: 10.1186/s12864-019-6066-6] [Cited by in Crossref: 5] [Cited by in F6Publishing: 14] [Article Influence: 1.7] [Reference Citation Analysis]
17 Upperman LR, Kinghorn BP, MacNeil MD, Van Eenennaam AL. Management of lethal recessive alleles in beef cattle through the use of mate selection software. Genet Sel Evol 2019;51:36. [PMID: 31382878 DOI: 10.1186/s12711-019-0477-3] [Cited by in Crossref: 5] [Cited by in F6Publishing: 9] [Article Influence: 1.7] [Reference Citation Analysis]
18 Mesbah-uddin M, Hoze C, Michot P, Barbat A, Lefebvre R, Boussaha M, Sahana G, Fritz S, Boichard D, Capitan A. A missense mutation (p.Tyr452Cys) in the CAD gene compromises reproductive success in French Normande cattle. Journal of Dairy Science 2019;102:6340-56. [DOI: 10.3168/jds.2018-16100] [Cited by in Crossref: 3] [Cited by in F6Publishing: 8] [Article Influence: 1.0] [Reference Citation Analysis]
19 Dreher C, Wellmann R, Stratz P, Schmid M, Preuß S, Hamann H, Bennewitz J. Genomic analysis of perinatal sucking reflex in German Brown Swiss calves. J Dairy Sci 2019;102:6296-305. [PMID: 31056319 DOI: 10.3168/jds.2019-16487] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
20 Iso-Touru T, Wurmser C, Venhoranta H, Hiltpold M, Savolainen T, Sironen A, Fischer K, Flisikowski K, Fries R, Vicente-Carrillo A, Alvarez-Rodriguez M, Nagy S, Mutikainen M, Peippo J, Taponen J, Sahana G, Guldbrandtsen B, Simonen H, Rodriguez-Martinez H, Andersson M, Pausch H. A splice donor variant in CCDC189 is associated with asthenospermia in Nordic Red dairy cattle. BMC Genomics 2019;20:286. [PMID: 30975085 DOI: 10.1186/s12864-019-5628-y] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]
21 Guarini AR, Sargolzaei M, Brito LF, Kroezen V, Lourenco DAL, Baes CF, Miglior F, Cole JB, Schenkel FS. Estimating the effect of the deleterious recessive haplotypes AH1 and AH2 on reproduction performance of Ayrshire cattle. J Dairy Sci 2019;102:5315-22. [PMID: 30954262 DOI: 10.3168/jds.2018-15366] [Cited by in Crossref: 3] [Cited by in F6Publishing: 7] [Article Influence: 1.0] [Reference Citation Analysis]
22 Zepeda-Batista JL, Parra-Bracamonte GM, Núñez-Domínguez R, Ramírez-Valverde R, Ruíz-Flores A. Screening genetic diseases prevalence in Braunvieh cattle. Trop Anim Health Prod 2019;51:25-31. [PMID: 30014197 DOI: 10.1007/s11250-018-1655-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 0.3] [Reference Citation Analysis]
23 Fritz S, Hoze C, Rebours E, Barbat A, Bizard M, Chamberlain A, Escouflaire C, Vander Jagt C, Boussaha M, Grohs C, Allais-bonnet A, Philippe M, Vallée A, Amigues Y, Hayes BJ, Boichard D, Capitan A. An initiator codon mutation in SDE2 causes recessive embryonic lethality in Holstein cattle. Journal of Dairy Science 2018;101:6220-31. [DOI: 10.3168/jds.2017-14119] [Cited by in Crossref: 10] [Cited by in F6Publishing: 12] [Article Influence: 2.5] [Reference Citation Analysis]
24 Frischknecht M, Bapst B, Seefried FR, Signer-Hasler H, Garrick D, Stricker C, Fries R, Russ I, Sölkner J, Bieber A, Strillacci MG, Gredler-Grandl B, Flury C; Intergenomics Consortium. Genome-wide association studies of fertility and calving traits in Brown Swiss cattle using imputed whole-genome sequences. BMC Genomics 2017;18:910. [PMID: 29178833 DOI: 10.1186/s12864-017-4308-z] [Cited by in Crossref: 19] [Cited by in F6Publishing: 22] [Article Influence: 3.8] [Reference Citation Analysis]
25 Rothammer S, Kunz E, Seichter D, Krebs S, Wassertheurer M, Fries R, Brem G, Medugorac I. Detection of two non-synonymous SNPs in SLC45A2 on BTA20 as candidate causal mutations for oculocutaneous albinism in Braunvieh cattle. Genet Sel Evol 2017;49:73. [PMID: 28982372 DOI: 10.1186/s12711-017-0349-7] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 2.4] [Reference Citation Analysis]
26 Michot P, Fritz S, Barbat A, Boussaha M, Deloche M, Grohs C, Hoze C, Le Berre L, Le Bourhis D, Desnoes O, Salvetti P, Schibler L, Boichard D, Capitan A. A missense mutation in PFAS (phosphoribosylformylglycinamidine synthase) is likely causal for embryonic lethality associated with the MH1 haplotype in Montbéliarde dairy cattle. Journal of Dairy Science 2017;100:8176-87. [DOI: 10.3168/jds.2017-12579] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 3.0] [Reference Citation Analysis]
27 Biffani S, Pausch H, Schwarzenbacher H, Biscarini F. The effect of mislabeled phenotypic status on the identification of mutation-carriers from SNP genotypes in dairy cattle. BMC Res Notes 2017;10:230. [PMID: 28651561 DOI: 10.1186/s13104-017-2540-x] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
28 Wu X, Guldbrandtsen B, Nielsen US, Lund MS, Sahana G. Association analysis for young stock survival index with imputed whole-genome sequence variants in Nordic Holstein cattle. J Dairy Sci 2017;100:6356-70. [PMID: 28551195 DOI: 10.3168/jds.2017-12688] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 1.6] [Reference Citation Analysis]
29 Breviario D. Is There any Alternative to Canonical DNA Barcoding of Multicellular Eukaryotic Species? A Case for the Tubulin Gene Family. Int J Mol Sci 2017;18:E827. [PMID: 28406446 DOI: 10.3390/ijms18040827] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
30 Pausch H, MacLeod IM, Fries R, Emmerling R, Bowman PJ, Daetwyler HD, Goddard ME. Evaluation of the accuracy of imputed sequence variant genotypes and their utility for causal variant detection in cattle. Genet Sel Evol 2017;49:24. [PMID: 28222685 DOI: 10.1186/s12711-017-0301-x] [Cited by in Crossref: 54] [Cited by in F6Publishing: 50] [Article Influence: 10.8] [Reference Citation Analysis]
31 Pausch H, Ammermüller S, Wurmser C, Hamann H, Tetens J, Drögemüller C, Fries R. A nonsense mutation in the COL7A1 gene causes epidermolysis bullosa in Vorderwald cattle. BMC Genet 2016;17:149. [PMID: 27905875 DOI: 10.1186/s12863-016-0458-2] [Cited by in Crossref: 20] [Cited by in F6Publishing: 12] [Article Influence: 3.3] [Reference Citation Analysis]
32 Biscarini F, Schwarzenbacher H, Pausch H, Nicolazzi EL, Pirola Y, Biffani S. Use of SNP genotypes to identify carriers of harmful recessive mutations in cattle populations. BMC Genomics 2016;17:857. [PMID: 27809787 DOI: 10.1186/s12864-016-3218-9] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.2] [Reference Citation Analysis]
33 Cole J, Null D, Vanraden P. Phenotypic and genetic effects of recessive haplotypes on yield, longevity, and fertility. Journal of Dairy Science 2016;99:7274-88. [DOI: 10.3168/jds.2015-10777] [Cited by in Crossref: 39] [Cited by in F6Publishing: 39] [Article Influence: 6.5] [Reference Citation Analysis]