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Keng Wee Teik

Observed names: K.W. Teik, Keng W. Teik, Wee-Teik Keng, Wee‐Teik Keng
ORCID: 0000-0003-3455-5285
Observed ORCID: 0000-0003-3455-5285
OpenAlex ID: A5048758322
Characterization of human disease phenotypes associated with mutations in TREX1 , RNASEH2A , RNASEH2B , RNASEH2C , SAMHD1 , ADAR , and IFIH1
2015 · Yanick J. Crow, Diana S. Chase, et al. · American Journal of Medical Genetics Part A · 608
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Genetic abnormalities in a large cohort of Coffin–Siris syndrome patients
2019 · Futoshi Sekiguchi, Yoshinori Tsurusaki, et al. · Journal of Human Genetics · 75
Efficient detection of copy‐number variations using exome data: Batch‐ and sex‐based analyses
2020 · Yuri Uchiyama, Daisuke Yamaguchi, et al. · Human Mutation · 36
Clinical variability and novel mutations in the NHEJ1 gene in patients with a Nijmegen breakage syndrome-like phenotype
2010 · Véronique Dutrannoy, Ilja Demuth, et al. · Human Mutation · 34
Autosomal recessive progeroid syndrome due to homozygosity for a TOMM7 variant
2022 · Abhimanyu Garg, Wee-Teik Keng, et al. · Journal of Clinical Investigation · 31
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Delineation of musculocontractural Ehlers–Danlos Syndrome caused by dermatan sulfate epimerase deficiency
2020 · Charlotte K. Lautrup, Keng W. Teik, et al. · Molecular Genetics & Genomic Medicine · 29
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Novel biallelic SZT2 mutations in 3 cases of early‐onset epileptic encephalopathy
2017 · N. Tsuchida, M. Nakashima, et al. · Clinical Genetics · 28
Novel Heterozygous Mutations in TALDO1 Gene Causing Transaldolase Deficiency and Early Infantile Liver Failure
2010 · S Balasubramaniam, Mirjam MC Wamelink, et al. · Journal of Pediatric Gastroenterology and Nutrition · 25
GRIN2D variants in three cases of developmental and epileptic encephalopathy
2018 · Naomi Tsuchida, Keisuke Hamada, et al. · Clinical Genetics · 24
Spectrum of germ-line RB1 gene mutations in Malaysian patients with retinoblastoma.
2015 · Mohd Khairul Nizam Mohd Khalid, Yusnita Yakob, et al. · PubMed Central · 24
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Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low‐to‐middle income Asian country
2022 · Yong‐Quan Lee, Sook‐Yee Yoon, et al. · Journal of Genetic Counseling · 21
Genetic Testing for Cancer Risk: Is the Community Willing to Pay for It?
2021 · Azimatun Noor Aizuddin, Abdul Rahman Ramdzan, et al. · International Journal of Environmental Research and Public Health · 16
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A homozygous missense variant in CHRM3 associated with familial urinary bladder disease
2019 · Glenda M. Beaman, Gabriella Galatà, et al. · Clinical Genetics · 14
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Early B-cell Factor 3–Related Genetic Disease Can Mimic Urofacial Syndrome
2020 · J. Robert Harkness, Glenda M. Beaman, et al. · Kidney International Reports · 12
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Cost-Effectiveness of Colorectal Cancer Genetic Testing
2021 · Abdul Rahman Ramdzan, Mohd Rizal Abdul Manaf, et al. · International Journal of Environmental Research and Public Health · 10
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Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy
2022 · Masamune Sakamoto, Kazuhiro Iwama, et al. · Genetics in Medicine · 8
Bullous ichthyosiform erythroderma, developmental delay, aortic and pulmonary stenosis in association with a FRA12A
2000 · Jonathan Berg, Elizabeth Grace, et al. · Clinical Dysmorphology · 6
NOVEL MUTATIONS OF THE G6PC GENE IN MALAYSIANS WITH GLYCOGEN STORAGE DISEASE 1a (GSD1a)
2021 · Amirah Assyiqqin Abd Rahman, Ili Syazwana Abdullah, et al. · Malaysian Journal of Science · 3
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Recurrent de novo variants in the spliceosomal factor CRNKL1 are associated with severe microcephaly and pontocerebellar hypoplasia with seizures
2025 · Sankalita Ray Das, Rosie Sullivan, et al. · The American Journal of Human Genetics · 1
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Intron retention is among six unreported AGL mutations identified in Malaysian GSD III patients
2019 · Ili Syazwana Abdullah, Ser-Huy Teh, et al. · Genes & Genomics · 1
Early B-cell Factor 3–Related Genetic Disease Can Mimic Urofacial Syndrome
2020 · J. Robert Harkness, Glenda M. Beaman, et al. · Newcastle University ePrints (Newcastle Univesity)
Author response for "GRIN2D variants in three cases of developmental and epileptic encephalopathy"
2018 · Naomi Tsuchida, Keisuke Hamada, et al. · Publons reviews and discussion
P33: A Report Of Two Life-Born Infants, Homozygous For Southeast Asian Ovalocytosis
2010 · Surini Yusoff, Narazah Mohd Yusoff, et al. · Malaysian Journal of Paediatrics and Child Health
Works count: 23
Citation count: 1,006
H-index: 13
I10-index: 15
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