Julia M. Paris

Bern, BE, Switzerland

Last Updated: 09/26/2026

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Found 12 publications

Is a heterozygous missense variant in SGSH the cause of a syndromic form of congenital amastia in an Original Braunvieh calf?

Is a heterozygous missense variant in SGSH the cause of a syndromic form of congenital amastia in an Original Braunvieh calf?

Journal: Animal genetics

Published: April 09, 2022

CNGB3 Missense Variant Causes Recessive Achromatopsia in Original Braunvieh Cattle.

CNGB3 Missense Variant Causes Recessive Achromatopsia in Original Braunvieh Cattle.

Journal: International journal of molecular sciences

Published: October 29, 2021

Genetic evaluation of small ruminant lentivirus susceptibility in Valais blacknose sheep.

Genetic evaluation of small ruminant lentivirus susceptibility in Valais blacknose sheep.

Journal: Animal genetics

Published: June 04, 2021

A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle.

A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle.

Journal: Genes

Published: June 02, 2021

A Nonsense Variant in Hephaestin Like 1 (HEPHL1) Is Responsible for Congenital Hypotrichosis in Belted Galloway Cattle.

A Nonsense Variant in Hephaestin Like 1 (HEPHL1) Is Responsible for Congenital Hypotrichosis in Belted Galloway Cattle.

Journal: Genes

Published: April 06, 2021

Analysis of Polycerate Mutants Reveals the Evolutionary Co-option of HOXD1 for Horn Patterning in Bovidae.

Analysis of Polycerate Mutants Reveals the Evolutionary Co-option of HOXD1 for Horn Patterning in Bovidae.

Journal: Molecular biology and evolution

Published: February 02, 2021

Compound heterozygous PLA2G6 loss-of-function variants in Swaledale sheep with neuroaxonal dystrophy.

Compound heterozygous PLA2G6 loss-of-function variants in Swaledale sheep with neuroaxonal dystrophy.

Journal: Molecular genetics and genomics : MGG

Published: September 17, 2020

Deleterious AGXT Missense Variant Associated with Type 1 Primary Hyperoxaluria (PH1) in Zwartbles Sheep.

Deleterious AGXT Missense Variant Associated with Type 1 Primary Hyperoxaluria (PH1) in Zwartbles Sheep.

Journal: Genes

Published: August 30, 2020

Ear type in sheep is associated with the MSRB3 locus.

Ear type in sheep is associated with the MSRB3 locus.

Journal: Animal genetics

Published: July 27, 2020

A de novo germline mutation of KIT in a white-spotted Brown Swiss cow.

A de novo germline mutation of KIT in a white-spotted Brown Swiss cow.

Journal: Animal genetics

Published: January 28, 2020

A de novo variant in OTX2 in a lamb with otocephaly.

A de novo variant in OTX2 in a lamb with otocephaly.

Journal: Acta veterinaria Scandinavica

Published: October 31, 2019

Identification of two TYRP1 loss-of-function alleles in Valais Red sheep.

Identification of two TYRP1 loss-of-function alleles in Valais Red sheep.

Journal: Animal genetics

Published: September 06, 2019

Showing 1-12 of 12

Last Updated: 09/26/2026