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For: Kunz E, Rothammer S, Pausch H, Schwarzenbacher H, Seefried FR, Matiasek K, Seichter D, Russ I, Fries R, Medugorac I. Confirmation of a non-synonymous SNP in PNPLA8 as a candidate causal mutation for Weaver syndrome in Brown Swiss cattle. Genet Sel Evol 2016;48:21. [PMID: 26992691 DOI: 10.1186/s12711-016-0201-5] [Cited by in Crossref: 20] [Cited by in F6Publishing: 14] [Article Influence: 3.3] [Reference Citation Analysis]
Number Citing Articles
1 Eck K, Kunz E, Mendel C, Lühken G, Medugorac I. Morphometric measurements in lambs as a basis for future mapping studies. Small Ruminant Research 2019;181:57-64. [DOI: 10.1016/j.smallrumres.2019.04.007] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
2 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] [Article Influence: 0.3] [Reference Citation Analysis]
3 Rothammer S, Kunz E, Krebs S, Bitzer F, Hauser A, Zinovieva N, Klymiuk N, Medugorac I. Remapping of the belted phenotype in cattle on BTA3 identifies a multiplication event as the candidate causal mutation. Genet Sel Evol 2018;50:36. [PMID: 29980171 DOI: 10.1186/s12711-018-0407-9] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
4 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: 28] [Article Influence: 5.5] [Reference Citation Analysis]
5 Xin WS, Zhang F, Yan GR, Xu WW, Xiao SJ, Zhang ZY, Huang LS. A whole genome sequence association study for puberty in a large Duroc × Erhualian F2 population. Anim Genet 2018;49:29-35. [PMID: 29194674 DOI: 10.1111/age.12623] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 1.2] [Reference Citation Analysis]
6 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]
7 Marina H, Chitneedi P, Pelayo R, Suárez-Vega A, Esteban-Blanco C, Gutiérrez-Gil B, Arranz JJ. Study on the concordance between different SNP-genotyping platforms in sheep. Anim Genet 2021;52:868-80. [PMID: 34515357 DOI: 10.1111/age.13139] [Reference Citation Analysis]
8 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: 27] [Article Influence: 6.5] [Reference Citation Analysis]
9 Ablondi M, Johnsson M, Eriksson S, Sabbioni A, Viklund ÅG, Mikko S. Performance of Swedish Warmblood fragile foal syndrome carriers and breeding prospects. Genet Sel Evol 2022;54:4. [PMID: 35062868 DOI: 10.1186/s12711-021-00693-4] [Reference Citation Analysis]
10 Ramljak J, Bunevski G, Bytyqi H, Marković B, Brka M, Ivanković A, Kume K, Stojanović S, Nikolov V, Simčič M, Sölkner J, Kunz E, Rothammer S, Seichter D, Grünenfelder HP, Broxham ET, Kugler W, Medugorac I. Conservation of a domestic metapopulation structured into related and partly admixed strains. Mol Ecol 2018;27:1633-50. [PMID: 29575253 DOI: 10.1111/mec.14555] [Cited by in Crossref: 14] [Cited by in F6Publishing: 12] [Article Influence: 3.5] [Reference Citation Analysis]
11 Gehrke LJ, Capitan A, Scheper C, König S, Upadhyay M, Heidrich K, Russ I, Seichter D, Tetens J, Medugorac I, Thaller G. Are scurs in heterozygous polled (Pp) cattle a complex quantitative trait? Genet Sel Evol 2020;52:6. [PMID: 32033534 DOI: 10.1186/s12711-020-0525-z] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
12 El-Sibai M, El Hajj J, Al Haddad M, El Baba N, Al Saneh M, Daoud Khatoun W, Helaers R, Vikkula M, El Atat O, Sabbagh J, Abou Chebel N, Ghassibe-Sabbagh M. Dysregulation of Rho GTPases in orofacial cleft patients-derived primary cells leads to impaired cell migration, a potential cause of cleft/lip palate development. Cells Dev 2021;165:203656. [PMID: 34024335 DOI: 10.1016/j.cdev.2021.203656] [Reference Citation Analysis]
13 Abitbol M, Jagannathan V, Laurent N, Noblet E, Dutil GF, Troupel T, de Dufaure de Citres C, Gache V, Blot S, Escriou C, Leeb T. A PNPLA8 frameshift variant in Australian shepherd dogs with hereditary ataxia. Anim Genet 2022. [PMID: 35864734 DOI: 10.1111/age.13245] [Reference Citation Analysis]
14 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]
15 Baes CF, Makanjuola BO, Miglior F, Marras G, Howard JT, Fleming A, Maltecca C. Symposium review: The genomic architecture of inbreeding: How homozygosity affects health and performance. Journal of Dairy Science 2019;102:2807-17. [DOI: 10.3168/jds.2018-15520] [Cited by in Crossref: 16] [Cited by in F6Publishing: 14] [Article Influence: 5.3] [Reference Citation Analysis]
16 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]
17 Goeckmann V, Rothammer S, Medugorac I. Bovine spastic paresis: A review of the genetic background and perspectives for the future. Vet J 2016;216:64-71. [PMID: 27687928 DOI: 10.1016/j.tvjl.2016.07.001] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
18 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: 4] [Article Influence: 1.7] [Reference Citation Analysis]
19 Müller MP, Rothammer S, Seichter D, Russ I, Hinrichs D, Tetens J, Thaller G, Medugorac I. Genome-wide mapping of 10 calving and fertility traits in Holstein dairy cattle with special regard to chromosome 18. J Dairy Sci 2017;100:1987-2006. [PMID: 28109604 DOI: 10.3168/jds.2016-11506] [Cited by in Crossref: 20] [Cited by in F6Publishing: 20] [Article Influence: 4.0] [Reference Citation Analysis]
20 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: 5] [Article Influence: 1.2] [Reference Citation Analysis]
21 Demir E, Bilginer U, Balcioglu MS, Karsli T. Direct and indirect contributions of molecular genetics to farm animal welfare: a review. Anim Health Res Rev 2021;:1-10. [PMID: 34842522 DOI: 10.1017/S1466252321000104] [Reference Citation Analysis]