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Mercè Garcia-Barceló
Observed names:
Merce Garcia-Barcelo,
Merce M Garcia-Barcelo,
Mercè Garcia-Barcelo,
Mercè Garcia-Barceló,
Mercè Garcia-Barcelo
Institution:
University of Hong Kong
Observed institutions:
Chinese University of Hong Kong,
Queen Mary Hospital,
University of Surrey,
Prince of Wales Hospital,
University of Hong Kong
OpenAlex ID:
A5113663103
Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases
2017
·
Philip C. Haycock
, Stephen Burgess
, et al.
·
JAMA Oncology
·
513
PDF
Differential Contributions of Rare and Common, Coding and Noncoding Ret Mutations to Multifactorial Hirschsprung Disease Liability
2010
·
Eileen Sproat Emison
, Merce Garcia-Barcelo
, et al.
·
The American Journal of Human Genetics
·
243
PDF
Hirschsprung's disease
2010
·
Simon E. Kenny
, Paul K.H. Tam
, et al.
·
Seminars in Pediatric Surgery
·
149
Genetic basis of Hirschsprung’s disease
2009
·
Paul K. H. Tam
, Mercè Garcia-Barceló
·
Pediatric Surgery International
·
124
TTF-1 and RET promoter SNPs: regulation of RET transcription in Hirschsprung's disease
2004
·
Mercè Garcia-Barcelo
, Raymond W. Ganster
, et al.
·
Human Molecular Genetics
·
101
Chromosomal mapping, tissue distribution and cDNA sequence of Four-and-a-half LIM domain protein 1 (FHL1)
1998
·
Simon Ming Yuen Lee
, Stephen Kwok Wing Tsui
, et al.
·
Gene
·
95
Genetic Analysis of the CYP2D6 Locus in a Hong Kong Chinese Population
2000
·
Mercè Garcia-Barceló
, Lok Yee Chow
, et al.
·
Clinical Chemistry
·
91
Isolation and chromosomal mapping of human glycogen synthase kinase-3 α and -3β encoding genes
1998
·
Pang-Chui Shaw
, Angela F Davies
, et al.
·
Genome
·
67
Highly Recurrent RET Mutations and Novel Mutations in Genes of the Receptor Tyrosine Kinase and Endothelin Receptor B Pathways in Chinese Patients with Sporadic Hirschsprung Disease
2004
·
Mercè Garcia-Barceló
, Mai-Har Sham
, et al.
·
Clinical Chemistry
·
60
Implications of Endocrine Gland–Derived Vascular Endothelial Growth Factor/Prokineticin-1 Signaling in Human Neuroblastoma Progression
2007
·
Elly S.W. Ngan
, Francesco Y.L. Sit
, et al.
·
Clinical Cancer Research
·
53
Characterization of the human 36-kDa carboxyl terminal LIM domain protein (hCLIM1)
1999
·
Masayo Kotaka
, Sai-Ming Ngai
, et al.
·
Journal of Cellular Biochemistry
·
49
Reduced RET expression in gut tissue of individuals carrying risk alleles of Hirschsprung's disease
2010
·
Xiaoping Miao
, Thomas Yuk-Yu Leon
, et al.
·
Human Molecular Genetics
·
47
Liver Intestine-Cadherin (CDH17) Haplotype Is Associated with Increased Risk of Hepatocellular Carcinoma
2006
·
Xiao Qi Wang
, John M. Luk
, et al.
·
Clinical Cancer Research
·
35
Molecular genetics of Hirschsprung’s disease
2004
·
Paul K.H. Tam
, Mercè Garcia-Barcelo
·
Seminars in Pediatric Surgery
·
34
Frequencies of Defective CYP2C19 Alleles in a Hong Kong Chinese Population: Detection of the Rare Allele CYP2C19*4
1999
·
Mercè Garcia-Barceló
, Lok-Yee Chow
, et al.
·
Clinical Chemistry
·
32
Mycobacterial DNA not detected in liver sections from patients with primary biliary cirrhosis
1998
·
John O'Donohue
, Helen Fidler
, et al.
·
Journal of Hepatology
·
28
Occurrence of CYP2D6 Gene Duplication in Hong Kong Chinese
2000
·
Mercè Garcia-Barceló
, Lok Yee Chow
, et al.
·
Clinical Chemistry
·
27
Population Differences in the Polyalanine Domain and 6 New Mutations in HLXB9 in Patients with Currarino Syndrome
2005
·
Mercè Garcia-Barceló
, Man-ting So
, et al.
·
Clinical Chemistry
·
25
PDF
Prophylactic thyroidectomy in ethnic Chinese patients with multiple endocrine neoplasia type 2A syndrome after the introduction of genetic testing.
2009
·
Gregory S K Lau
, Brian H H Lang
, et al.
·
PubMed
·
21
PDF
A complementary study approach unravels novel players in the pathoetiology of Hirschsprung disease
2020
·
Tanja Mederer
, Stefanie Schmitteckert
, et al.
·
PLoS Genetics
·
12
PDF
Epidemiological characteristics of Hirschsprung’s disease (HSCR): Results of a case series of fifty patients from Bangladesh
2018
·
Anwarul Karim
, Mastura Akter
, et al.
·
Journal of Pediatric Surgery
·
10
Are psychiatric comorbidities and associated cognitive functions related to treatment response to methylphenidate in boys with attention-deficit/hyperactivity disorder?
2017
·
Mandy H Chan
, Patrick WL Leung
, et al.
·
Neuropsychiatric Disease and Treatment
·
10
PDF
Male and female differential reproductive rate could explain parental transmission asymmetry of mutation origin in Hirschsprung disease
2012
·
Anne-Sophie Jannot
, Jeanne Amiel
, et al.
·
European Journal of Human Genetics
·
10
Application of HapMap data to the evaluation of 8 candidate genes for pediatric slow transit constipation
2007
·
Mercè Garcia-Barcelo
, Sebastian K. King
, et al.
·
Journal of Pediatric Surgery
·
10
Schizophrenia and Hypocalcaemia: Variable Phenotype of Deletion at Chromosome 22q11
1999
·
L.Y. Chow
, Merce Garcia-Barcelo
, et al.
·
Australian & New Zealand Journal of Psychiatry
·
7
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Works count:
29
Citation count:
1,862
H-index:
19
I10-index:
24
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