Atsushi Fujita

Yokohama, Japan

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 176 publications

Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.

Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.

Journal: Clinical genetics

Published: June 05, 2026

Short-term outcomes of open liver lobectomy using an Endo GIA stapler: case series of five cats.

Short-term outcomes of open liver lobectomy using an Endo GIA stapler: case series of five cats.

Journal: Journal of feline medicine and surgery

Published: March 27, 2026

CUBN-AMN pathway loss in chronic benign proteinuria.

CUBN-AMN pathway loss in chronic benign proteinuria.

Journal: Kidney international

Published: January 27, 2026

Cyclogram analysis of canine gait: quantifying inter-joint coordination and clinical utility in rehabilitation.

Cyclogram analysis of canine gait: quantifying inter-joint coordination and clinical utility in rehabilitation.

Journal: Frontiers in veterinary science

Published: January 08, 2026

Correction: Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability.

Correction: Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability.

Journal: Journal of human genetics

Published: November 09, 2025

Monoallelic and biallelic RNU4-2 variants in neurodevelopmental disorders.

Monoallelic and biallelic RNU4-2 variants in neurodevelopmental disorders.

Journal: Journal of human genetics

Published: October 27, 2025

ZMYND11 p.Arg600Trp variant associated with a distinctive neurodevelopmental phenotype.

ZMYND11 p.Arg600Trp variant associated with a distinctive neurodevelopmental phenotype.

Journal: Human genome variation

Published: October 20, 2025

The outcomes of Swenson's pull-through in six cats with colorectal adenocarcinoma.

The outcomes of Swenson's pull-through in six cats with colorectal adenocarcinoma.

Journal: The Journal of veterinary medical science

Published: September 24, 2025

Biallelic variants in TNR cause neurodevelopmental disorders with variable expressivity.

Biallelic variants in TNR cause neurodevelopmental disorders with variable expressivity.

Journal: Journal of human genetics

Published: September 08, 2025

Long-read genomic analyses to elucidate hidden structural variations associated with MECP2 duplication syndrome.

Long-read genomic analyses to elucidate hidden structural variations associated with MECP2 duplication syndrome.

Journal: Journal of human genetics

Published: September 06, 2025

Identification of myokymia in adult-onset hereditary spastic paraplegia type 79A: Implications for the phenotypic spectrum.

Identification of myokymia in adult-onset hereditary spastic paraplegia type 79A: Implications for the phenotypic spectrum.

Journal: eNeurologicalSci

Published: August 14, 2025

Completely resolved structural variants by optical genome mapping with adaptive sampling from CNV discovery.

Completely resolved structural variants by optical genome mapping with adaptive sampling from CNV discovery.

Journal: NPJ genomic medicine

Published: August 14, 2025

Showing 1-12 of 176

Last Updated: 09/26/2026