Jennifer A. West

288 Herston Road
Herston, QLD 4006, Australia

Last Updated: 09/26/2026

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Found 14 publications

CD33 and clusterin interact biophysically and genetically to modulate Alzheimer risk.

CD33 and clusterin interact biophysically and genetically to modulate Alzheimer risk.

Journal: Nature communications

Published: February 17, 2026

CD33 and clusterin interact biophysically and genetically to modulate Alzheimer risk.

CD33 and clusterin interact biophysically and genetically to modulate Alzheimer risk.

Journal: Nature communications

Published: February 17, 2026

CD33 and clusterin interact biophysically and genetically to modulate Alzheimer risk.

CD33 and clusterin interact biophysically and genetically to modulate Alzheimer risk.

Journal: bioRxiv : the preprint server for biology

Published: August 06, 2025

Fibrillin-1 and asprosin, novel players in metabolic syndrome.

Fibrillin-1 and asprosin, novel players in metabolic syndrome.

Journal: Molecular genetics and metabolism

Published: September 08, 2022

Neuroserpin and transthyretin are extracellular chaperones that preferentially inhibit amyloid formation.

Neuroserpin and transthyretin are extracellular chaperones that preferentially inhibit amyloid formation.

Journal: Science advances

Published: December 10, 2021

The impact of Marfan syndrome on an Aboriginal Australian family: 'I don't like it as much as I don't like cancer'.

The impact of Marfan syndrome on an Aboriginal Australian family: 'I don't like it as much as I don't like cancer'.

Journal: Journal of genetic counseling

Published: February 28, 2021

Microdeletion of 9q22.3: A patient with minimal deletion size associated with a severe phenotype.

Microdeletion of 9q22.3: A patient with minimal deletion size associated with a severe phenotype.

Journal: American journal of medical genetics. Part A

Published: December 23, 2020

Causal Attributions in an Australian Aboriginal Family With Marfan Syndrome: A Qualitative Study.

Causal Attributions in an Australian Aboriginal Family With Marfan Syndrome: A Qualitative Study.

Journal: Frontiers in genetics

Published: December 03, 2019

Use of the arm-span to height ratio as a criterion for Marfan syndrome in Aboriginal Australians: Diagnostically challenging.

Use of the arm-span to height ratio as a criterion for Marfan syndrome in Aboriginal Australians: Diagnostically challenging.

Journal: American journal of medical genetics. Part A

Published: October 22, 2019

Compound heterozygous mutations in FBN1 in a large family with Marfan syndrome.

Compound heterozygous mutations in FBN1 in a large family with Marfan syndrome.

Journal: Molecular genetics & genomic medicine

Published: September 15, 2019

Polyclonal T-cells express CD1a in Langerhans cell histiocytosis (LCH) lesions.

Polyclonal T-cells express CD1a in Langerhans cell histiocytosis (LCH) lesions.

Journal: PloS one

Published: May 29, 2014

Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome.

Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome.

Journal: BoneKEy reports

Published: August 07, 2013

Showing 1-12 of 14

Last Updated: 09/26/2026