Becker D - Search Results

1

Candidate Genetic Modifiers for RPGR Retinal Degeneration.

Appelbaum T, Murgiano L, Becker D, Santana E, Aguirre GD. Appelbaum T, et al. Among authors: becker d. Invest Ophthalmol Vis Sci. 2020 Dec 1;61(14):20. doi: 10.1167/iovs.61.14.20. Invest Ophthalmol Vis Sci. 2020. PMID: 33326016 Free PMC article.

2

Molecular studies of phenotype variation in canine RPGR-XLPRA1.

Appelbaum T, Becker D, Santana E, Aguirre GD. Appelbaum T, et al. Among authors: becker d. Mol Vis. 2016 Apr 9;22:319-31. eCollection 2016. Mol Vis. 2016. PMID: 27122963 Free PMC article.

3

Complex Structural PPT1 Variant Associated with Non-syndromic Canine Retinal Degeneration.

Murgiano L, Becker D, Torjman D, Niggel JK, Milano A, Cullen C, Feng R, Wang F, Jagannathan V, Pearce-Kelling S, Katz ML, Leeb T, Aguirre GD. Murgiano L, et al. Among authors: becker d. G3 (Bethesda). 2019 Feb 7;9(2):425-437. doi: 10.1534/g3.118.200859. G3 (Bethesda). 2019. PMID: 30541930 Free PMC article.

4

Optic nerve hypoplasia in miniature poodle dogs: A preliminary genetic and candidate gene association study.

Becker D, Niggel JK, Pearce-Kelling S, Riis RC, Aguirre GD. Becker D, et al. Vet Ophthalmol. 2020 Jan;23(1):67-76. doi: 10.1111/vop.12691. Epub 2019 Jul 25. Vet Ophthalmol. 2020. PMID: 31342635 Free PMC article.

5

Genome-wide association study and whole-genome sequencing identify a deletion in LRIT3 associated with canine congenital stationary night blindness.

Das RG, Becker D, Jagannathan V, Goldstein O, Santana E, Carlin K, Sudharsan R, Leeb T, Nishizawa Y, Kondo M, Aguirre GD, Miyadera K. Das RG, et al. Among authors: becker d. Sci Rep. 2019 Oct 2;9(1):14166. doi: 10.1038/s41598-019-50573-7. Sci Rep. 2019. PMID: 31578364 Free PMC article.

6

A genome-wide significant association on chromosome 15 for congenital entropion in Swiss White Alpine sheep.

Hirter N, Letko A, Häfliger IM, Becker D, Greber D, Drögemüller C. Hirter N, et al. Among authors: becker d. Anim Genet. 2020 Mar;51(2):278-283. doi: 10.1111/age.12903. Epub 2020 Jan 16. Anim Genet. 2020. PMID: 31945208

7

CCDC66 frameshift variant associated with a new form of early-onset progressive retinal atrophy in Portuguese Water Dogs.

Murgiano L, Becker D, Spector C, Carlin K, Santana E, Niggel JK, Jagannathan V, Leeb T, Pearce-Kelling S, Aguirre GD, Miyadera K. Murgiano L, et al. Among authors: becker d. Sci Rep. 2020 Dec 3;10(1):21162. doi: 10.1038/s41598-020-77980-5. Sci Rep. 2020. PMID: 33273526 Free PMC article.

8

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. Ekenstedt KJ, et al. Among authors: becker d. PLoS Genet. 2014 Oct 2;10(10):e1004635. doi: 10.1371/journal.pgen.1004635. eCollection 2014 Oct. PLoS Genet. 2014. PMID: 25275565 Free PMC article.

9

Canine NAPEPLD-associated models of human myelin disorders.

Minor KM, Letko A, Becker D, Drögemüller M, Mandigers PJJ, Bellekom SR, Leegwater PAJ, Stassen QEM, Putschbach K, Fischer A, Flegel T, Matiasek K, Ekenstedt KJ, Furrow E, Patterson EE, Platt SR, Kelly PA, Cassidy JP, Shelton GD, Lucot K, Bannasch DL, Martineau H, Muir CF, Priestnall SL, Henke D, Oevermann A, Jagannathan V, Mickelson JR, Drögemüller C. Minor KM, et al. Among authors: becker d. Sci Rep. 2018 Apr 11;8(1):5818. doi: 10.1038/s41598-018-23938-7. Sci Rep. 2018. PMID: 29643404 Free PMC article.

10

A 50-kb deletion disrupting the RSPO2 gene is associated with tetradysmelia in Holstein Friesian cattle.

Becker D, Weikard R, Schulze C, Wohlsein P, Kühn C. Becker D, et al. Genet Sel Evol. 2020 Nov 11;52(1):68. doi: 10.1186/s12711-020-00586-y. Genet Sel Evol. 2020. PMID: 33176673 Free PMC article.

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