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Author Details
Full Name
Monnat Pongpanich
Affiliation
Chulalongkorn University
ORCID
Career Start Year
2010
Papers
29
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37994247
Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8.
Mov Disord
2024
37320968
Long-read Nanopore sequencing identified D4Z4 contractions in patients with facioscapulohumeral muscular dystrophy.
Neuromuscul Disord
2023
37765454
Genome-Wide Association Study of Starch Properties in Local Thai Rice.
Plants (Basel)
2023
34994516
Salt stress responses and SNP-based phylogenetic analysis of Thai rice cultivars.
Plant Genome
2022
35664831
The roles of HMGB1-produced DNA gaps in DNA protection and aging biomarker reversal.
FASEB Bioadv
2022
35363313
Long-read Amplicon Sequencing of the CYP21A2 in 48 Thai Patients With Steroid 21-Hydroxylase Deficiency.
J Clin Endocrinol Metab
2022
36327219
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.
PLoS Genet
2022
35163767
Identification of a Negative Regulator for Salt Tolerance at Seedling Stage via a Genome-Wide Association Study of Thai Rice Populations.
Int J Mol Sci
2022
35013560
Host genetic factors of COVID-19 susceptibility and disease severity in a Thai population.
J Hum Genet
2022
35176049
Genotypic and phenotypic landscapes of 51 pharmacogenes derived from whole-genome sequencing in a Thai population.
PLoS One
2022
33022811
An integrative analysis of genome-wide methylation and expression in ameloblastoma: A pilot study.
Oral Dis
2021
34231238
Whole genome sequencing identifies a homozygous nonsense mutation in the JPH2 gene in Shih Tzu dogs with progressive retinal atrophy.
Anim Genet
2021
32973343
Founder effect of the TTTCA repeat insertions in SAMD12 causing BAFME1.
Eur J Hum Genet
2021
33144648
Phenotype prediction and characterization of 25 pharmacogenes in Thais from whole genome sequencing for clinical implementation.
Sci Rep
2020
31998290
Profile of Histone H3 Lysine 4 Trimethylation and the Effect of Lipopolysaccharide/Immune Complex-Activated Macrophages on Endotoxemia.
Front Immunol
2020
30669971
Genome-wide association study for salinity tolerance at the flowering stage in a panel of rice accessions from Thailand.
BMC Genomics
2019
31349693
Comparative Genomic Analysis of Rice with Contrasting Photosynthesis and Grain Production under Salt Stress.
Genes (Basel)
2019
31539032
TTTCA repeat insertions in an intron of YEATS2 in benign adult familial myoclonic epilepsy type 4.
Brain
2019
29336607
Alu siRNA to increase Alu element methylation and prevent DNA damage.
Epigenomics
2018
29812972
Reduction in replication-independent endogenous DNA double-strand breaks promotes genomic instability during chronological aging in yeast.
FASEB J
2018
30410502
Pathologic Replication-Independent Endogenous DNA Double-Strand Breaks Repair Defect in Chronological Aging Yeast.
Front Genet
2018
28257626
Two novel compound heterozygous BMP1 mutations in a patient with osteogenesis imperfecta: a case report.
BMC Med Genet
2017
26985960
Whole-exome sequencing reveals a novel COL2A1 mutation in a patient with spondylo-epiphyseal dysplasia congenita.
Genet Mol Res
2016
27955642
Short stature, platyspondyly, hip dysplasia, and retinal detachment: an atypical type II collagenopathy caused by a novel mutation in the C-propeptide region of COL2A1: a case report.
BMC Med Genet
2016
25179264
Characteristics of replication-independent endogenous double-strand breaks in Saccharomyces cerevisiae.
BMC Genomics
2014
23935075
Upstream mononucleotide A-repeats play a cis-regulatory role in mammals through the DICER1 and Ago proteins.
Nucleic Acids Res
2013
22303404
On the Aggregation of Multimarker Information for Marker-Set and Sequencing Data Analysis: Genotype Collapsing vs. Similarity Collapsing.
Front Genet
2012
21835306
Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression.
Am J Hum Genet
2011
20501555
A quality control algorithm for filtering SNPs in genome-wide association studies.
Bioinformatics
2010
1 - 29 of 29
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Nicole Simons
Icahn School of Medicine at Mount Sinai
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Efren Sandoval
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