Author

Lip Hen Moey

Observed names: L.H. Moey, Lip H. Moey, Lip-Hen Moey, Moey, Lip-Hen

Institution: Hospital Pulau Pinang

Observed institutions: Ministry of Health, Hospital Kuala Lumpur, Hospital Pulau Pinang, Children's Hospital at Westmead, Westmead Hospital

ORCID: 0000-0002-5516-0592

Observed ORCID: 0000-0002-5516-0592

OpenAlex ID: A5047909605

Fructose-1,6-bisphosphatase deficiency as a cause of recurrent hypoglycemia and metabolic acidosis: Clinical and molecular findings in Malaysian patients

2017 · Lip Hen Moey, Nor Azimah Abdul Azize, et al. · Pediatrics & Neonatology · 25

Oncologist-led BRCA counselling improves access to cancer genetic testing in middle-income Asian country, with no significant impact on psychosocial outcomes

2021 · Sook-Yee Yoon, Siu Wan Wong, et al. · Journal of Medical Genetics · 24

Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt

2024 · James L. Shepherdson, Katie Hutchison, et al. · The American Journal of Human Genetics · 21

Biallelic null variants in ZNF142 cause global developmental delay with familial epilepsy and dysmorphic features

2021 · Shinichi Kameyama, Takeshi Mizuguchi, et al. · Journal of Human Genetics · 13

A novel homozygous truncating variant of NECAP1 in early infantile epileptic encephalopathy: the second case report of EIEE21

2019 · Takeshi Mizuguchi, Mitsuko Nakashima, et al. · Journal of Human Genetics · 8

Biallelic loss-of-function variants in ZNF142 are associated with a robust DNA methylation signature affecting a limited number of genomic loci

2025 · Mathis Hildonen, Andrea Ciolfi, et al. · European Journal of Human Genetics · 5

Optic disc swelling in acromicric and geleophysic dysplasia

2019 · Lip Hen Moey, Maree Flaherty, et al. · American Journal of Medical Genetics Part A · 5

A first large study of whole-exome sequencing (WES) in 489 patients with suspected rare genetic disorders at a tertiary centre in Malaysia

2025 · Lip Hen Moey, Go Hun Seo, et al. · Rare · 3

Monoallelic and biallelic RNU4-2 variants in neurodevelopmental disorders

2025 · Yukina Hayashi, Kenta Kajiwara, et al. · Journal of Human Genetics · 2

Clinical, biochemical, molecular characteristics and clinical outcome of hyperhomocysteinemia in Malaysian children

2024 · Anasufiza Habib, Hamizah Idrus, et al. · Clinical Biochemistry · 1

Spectrum of inherited hyperhomocysteinemia in Malaysia

2024 · A. Habib, H. Idrus, et al. · Clinica Chimica Acta

Germline BRCA1 and BRCA2 variants in a population based cohort of ovarian, peritoneal or fallopian tube cancer patients in Malaysia

2017 · Joanna Lim, S.Y. Lau, et al. · DOAJ (DOAJ: Directory of Open Access Journals)

Psychosocial aspects of mainstreaming genetic counselling for genetic testing of BRCA1 and BRCA2 in ovarian cancer patients in Malaysia (MaGiC)

2017 · Siu Wan Wong, N.S. Ahmad Bashah, et al. · DOAJ (DOAJ: Directory of Open Access Journals)

Works count: 14

Citation count: 107

H-index: 5

I10-index: 4