Thipwimol Tim-Aroon

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 11

Top Topics

Peritoneal Dialysis

Intellectual Disability

Autism Spectrum Disorder

Prognostic Factors

Top Venues

American journal of medical genetics. Part A

Molecular genetics & genomic medicine

Scientific reports

Orphanet journal of rare diseases

This page only lists publications with an associated author ORCID identifier.

Publications

Saisuda Noojarern, Thipwimol Tim-Aroon, Kingthong Anurat, Tim Phetthong, Arthaporn Khongkraparn, Duangrurdee Wattanasirichaigoon
A novel AP1S2 variant causing leaky splicing in X-linked intellectual disability: Further delineation and intrafamilial variability. American journal of medical genetics. Part A 194 (9) (2024)
Saisuda Noojarern, Thipwimol Tim-Aroon, Kingthong Anurat, Tim Phetthong, Arthaporn Khongkraparn, Duangrurdee Wattanasirichaigoon
A novel AP1S2 variant causing leaky splicing in X-linked intellectual disability: Further delineation and intrafamilial variability. American journal of medical genetics. Part A 194 (9) (2024)
Saisuda Noojarern, Thipwimol Tim-Aroon, Kingthong Anurat, Tim Phetthong, Arthaporn Khongkraparn, Duangrurdee Wattanasirichaigoon
A novel AP1S2 variant causing leaky splicing in X-linked intellectual disability: Further delineation and intrafamilial variability. American journal of medical genetics. Part A 194 (9) (2024)
Saisuda Noojarern, Thipwimol Tim-Aroon, Kingthong Anurat, Tim Phetthong, Arthaporn Khongkraparn, Duangrurdee Wattanasirichaigoon
A novel AP1S2 variant causing leaky splicing in X-linked intellectual disability: Further delineation and intrafamilial variability. American journal of medical genetics. Part A (2024)
Kalyarat Wilaiwongsathien, Duangrurdee Wattanasirichaigoon, Sasivimol Rattanasiri, Chanatpon Aonnuam, Chayada Tangshewinsirikul, Thipwimol Tim-Aroon
Parental Awareness, Knowledge, and Attitudes Regarding Current and Future Newborn Bloodspot Screening: The First Report from Thailand. International journal of neonatal screening 9 (2) (2023)
Songpon Getsuwan, Pornthep Tanpowpong, Chatmanee Lertudomphonwanit, Thitiporn Junhasavasdikul, Thipwimol Tim-Aroon, Suporn Treepongkaruna
Etiology and outcome of acute recurrent pancreatitis and chronic pancreatitis. Pediatrics international : official journal of the Japan Pediatric Society 64 (1) (2022)
Tim Phetthong, Thipwimol Tim-Aroon, Arthaporn Khongkrapan, Preamrudee Poomthavorn, Duangrurdee Wattanasirichaigoon
Kabuki syndrome with midgut malrotation and hyperinsulinemic hypoglycemia: A rare co-occurrence from Thailand. American journal of medical genetics. Part A 182 (8) (2020)
Nantiya Mongkollarp, Thipwimol Tim-Aroon, Chusak Okascharoen, Khunton Wichajarn, Jeeraparn Phosuwattanakul, Nalinee Chongviriyaphan, Duangrurdee Wattanasirichaigoon
Growth charts for Thai children with Prader-Willi syndrome aged 0-18 years. Orphanet journal of rare diseases 15 (1) (2020)
Songpon Getsuwan, Chatmanee Lertudomphonwanit, Pornthep Tanpowpong, Chollasak Thirapattaraphan, Thipwimol Tim-Aroon, Duangrurdee Wattanasirichaigoon, Suporn Treepongkaruna
Etiologies, Prognostic Factors, and Outcomes of Pediatric Acute Liver Failure in Thailand. Pediatric gastroenterology, hepatology & nutrition 23 (6) (2020)
Kitiwan Rojnueangnit, Chariyawan Charalsawadi, Weerin Thammachote, Ariya Pradabmuksiri, Thipwimol Tim-Aroon, Antonio Novelli, Sara Loddo, Silvana Briuglia, Cutrupi M Concetta, Duangrurdee Wattanasirichaigoon, Natini Jinawath
Clinical delineation of 18q11-q12 microdeletion: Intellectual disability, speech and behavioral disorders, and conotruncal heart defects. Molecular genetics & genomic medicine 7 (9) (2019)
Areerat Hnoonual, Weerin Thammachote, Thipwimol Tim-Aroon, Kitiwan Rojnueangnit, Tippawan Hansakunachai, Tasanawat Sombuntham, Rawiwan Roongpraiwan, Juthamas Worachotekamjorn, Jariya Chuthapisith, Suthat Fucharoen, Duangrurdee Wattanasirichaigoon, Nichara Ruangdaraganon, Pornprot Limprasert, Natini Jinawath
Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder. Scientific reports 7 (1) (2017)