Duangrurdee Wattanasirichaigoon

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 24

Top Venues

Pediatric blood & cancer

American journal of medical genetics. Part A

International journal of environmental research and public health

BMC pediatrics

Royal Thai Government Ministry of Public Health

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

Affiliation History

Royal Thai Government Ministry of Public Health Apr 01 1988 - Mar 31 1990

Thailand

General Practitioner :: Yasothorn General Hospital, Pediatrics

Royal Thai Government Ministry of Public Health Apr 01 1987 - Mar 31 1988

Thailand

General Practitioner :: Patew Distric Hospital

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)
Takeya Adachi, Ayman W. El-Hattab, Ritu Jain, Katya A Nogales Crespo, Camila I Quirland Lazo, Maurizio Scarpa, Marshall Summar, Duangrurdee Wattanasirichaigoon
Enhancing Equitable Access to Rare Disease Diagnosis and Treatment around the World: A Review of Evidence, Policies, and Challenges. International journal of environmental research and public health 20 (6) (2023)
Takeya Adachi, Ayman W. El-Hattab, Ritu Jain, Katya A Nogales Crespo, Camila I Quirland Lazo, Maurizio Scarpa, Marshall Summar, Duangrurdee Wattanasirichaigoon
Enhancing Equitable Access to Rare Disease Diagnosis and Treatment around the World: A Review of Evidence, Policies, and Challenges. International journal of environmental research and public health 20 (6) (2023)
Takeya Adachi, Ayman W. El-Hattab, Ritu Jain, Katya A Nogales Crespo, Camila I Quirland Lazo, Maurizio Scarpa, Marshall Summar, Duangrurdee Wattanasirichaigoon
Enhancing Equitable Access to Rare Disease Diagnosis and Treatment around the World: A Review of Evidence, Policies, and Challenges. International journal of environmental research and public health 20 (6) (2023)
Usanarat Anurathapan, Thipwimol Tim-Aroon, Wujuan Zhang, Watinee Sanpote, Siranee Wongrungsri, Nitcha Khunin, Somchai Chutipongtanate, Vilawan Chirdkiatgumchai, Lukana Ngiwsara, Suphaneewan Jaovisidha, Arthaporn Khongkraparn, Samart Pakakasama, Jisnuson Svasti, Kenneth D R Setchell, Duangrurdee Wattanasirichaigoon, Suradej Hongeng
Comprehensive and long-term outcomes of enzyme replacement therapy followed by stem cell transplantation in children with Gaucher disease type 1 and 3. Pediatric blood & cancer 70 (3) (2022)
Usanarat Anurathapan, Thipwimol Tim-Aroon, Wujuan Zhang, Watinee Sanpote, Siranee Wongrungsri, Nitcha Khunin, Somchai Chutipongtanate, Vilawan Chirdkiatgumchai, Lukana Ngiwsara, Suphaneewan Jaovisidha, Arthaporn Khongkraparn, Samart Pakakasama, Jisnuson Svasti, Kenneth D R Setchell, Duangrurdee Wattanasirichaigoon, Suradej Hongeng
Comprehensive and long-term outcomes of enzyme replacement therapy followed by stem cell transplantation in children with Gaucher disease type 1 and 3. Pediatric blood & cancer 70 (3) (2022)
Usanarat Anurathapan, Thipwimol Tim-Aroon, Wujuan Zhang, Watinee Sanpote, Siranee Wongrungsri, Nitcha Khunin, Somchai Chutipongtanate, Vilawan Chirdkiatgumchai, Lukana Ngiwsara, Suphaneewan Jaovisidha, Arthaporn Khongkraparn, Samart Pakakasama, Jisnuson Svasti, Kenneth D R Setchell, Duangrurdee Wattanasirichaigoon, Suradej Hongeng
Comprehensive and long-term outcomes of enzyme replacement therapy followed by stem cell transplantation in children with Gaucher disease type 1 and 3. Pediatric blood & cancer 70 (3) (2022)
Usanarat Anurathapan, Thipwimol Tim-Aroon, Wujuan Zhang, Watinee Sanpote, Siranee Wongrungsri, Nitcha Khunin, Somchai Chutipongtanate, Vilawan Chirdkiatgumchai, Lukana Ngiwsara, Suphaneewan Jaovisidha, Arthaporn Khongkraparn, Samart Pakakasama, Jisnuson Svasti, Kenneth D R Setchell, Duangrurdee Wattanasirichaigoon, Suradej Hongeng
Comprehensive and long-term outcomes of enzyme replacement therapy followed by stem cell transplantation in children with Gaucher disease type 1 and 3. Pediatric blood & cancer (2022)
Pongpak Pongphitcha, Nongnuch Sirachainan, Arthaporn Khongkraparn, Thipwimol Tim-Aroon, Duantida Songdej, Duangrurdee Wattanasirichaigoon
A novel TCN2 mutation with unusual clinical manifestations of hemolytic crisis and unexplained metabolic acidosis: expanding the genotype and phenotype of transcobalamin II deficiency. BMC pediatrics 22 (1) (2022)
Usanarat Anurathapan, Thipwimol Tim-Aroon, Wujuan Zhang, Watinee Sanpote, Siranee Wongrungsri, Nitcha Khunin, Somchai Chutipongtanate, Vilawan Chirdkiatgumchai, Lukana Ngiwsara, Suphaneewan Jaovisidha, Arthaporn Khongkraparn, Samart Pakakasama, Jisnuson Svasti, Kenneth D R Setchell, Duangrurdee Wattanasirichaigoon, Suradej Hongeng
Comprehensive and long-term outcomes of enzyme replacement therapy followed by stem cell transplantation in children with Gaucher disease type 1 and 3. Pediatric blood & cancer 70 (3) (2022)
Wuttichart Kamolvisit, Prasit Phowthongkum, Ponghatai Boonsimma, Chulaluck Kuptanon, Kitiwan Rojnueangnit, Duangrurdee Wattanasirichaigoon, Mongkol Chanvanichtrakool, Chutima Phuaksaman, Pattara Wiromrat, Chalurmpon Srichomthong, Chupong Ittiwut, Chureerat Phokaew, Rungnapa Ittiwut, Adjima Assawapitaksakul, Wanna Chetruengchai, Aayalida Buasong, Kanya Suphapeetiporn, Vorasuk Shotelersuk
Rapid exome sequencing as the first-tier investigation for diagnosis of acutely and severely ill children and adults in Thailand. Clinical genetics 100 (1) (2021)
Tim Phetthong, Thipwimol Tim-Aroon, Arthaporn Khongkraparn, Saisuda Noojarern, Chulaluck Kuptanon, Khunton Wichajarn, Achara Sathienkijkanchai, Kanya Suphapeetiporn, Pimlak Charoenkwan, Adisak Tantiworawit, Naruwan Noentong, Duangrurdee Wattanasirichaigoon
Gaucher disease: clinical phenotypes and refining GBA mutational spectrum in Thai patients. Orphanet journal of rare diseases 16 (1) (2021)
Thipwimol Tim-Aroon, Khunton Wichajarn, Kamornwan Katanyuwong, Pranoot Tanpaiboon, Nithiwat Vatanavicharn, Kullasate Sakpichaisakul, Arthaporn Kongkrapan, Jakris Eu-Ahsunthornwattana, Supranee Thongpradit, Kanya Moolsuwan, Nusara Satproedprai, Surakameth Mahasirimongkol, Tassanee Lerksuthirat, Bhoom Suktitipat, Natini Jinawath, Duangrurdee Wattanasirichaigoon
Infantile onset Sandhoff disease: clinical manifestation and a novel common mutation in Thai patients. BMC pediatrics 21 (1) (2021)
Tim Phetthong, Arthaporn Khongkrapan, Natini Jinawath, Go-Hun Seo, Duangrurdee Wattanasirichaigoon
Compound Heterozygote of Point Mutation and Chromosomal Microdeletion Involving OTUD6B Coinciding with ZMIZ1 Variant in Syndromic Intellectual Disability. Genes 12 (10) (2021)
Chayada Tangshewinsirikul, Wirada Dulyaphat, Sanpon Diawtipsukon, Yada Tingthanatikul, Chonthicha Satirapod, Duangrurdee Wattanasirichaigoon
Successful pregnancy outcome in Herlyn-Werner-Wunderlich syndrome with pyocolpos: A case report and literature review. Clinical case reports 8 (11) (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)
Chalongchai Chalermwat, Thitipa Thosapornvichai, Laran T Jensen, Duangrurdee Wattanasirichaigoon
Genetic Analysis of Peroxisomal Genes Required for Longevity in a Yeast Model of Citrin Deficiency. Diseases (Basel, Switzerland) 8 (1) (2020)
Sukrit Suwannachat, Duangrurdee Wattanasirichaigoon, Jiraporn Arunakul, Vilawan Chirdkiatgumchai, Thipwimol Tim-Aroon
Perspectives of adults with Klinefelter syndrome, unaffected adolescent males, and parents of affected children toward diagnosis disclosure: a Thai experience. Journal of community genetics 11 (2) (2019)
Lukana Ngiwsara, Duangrurdee Wattanasirichaigoon, Thipwimol Tim-Aroon, Kitiwan Rojnueangnit, Saisuda Noojaroen, Arthaporn Khongkraparn, Phannee Sawangareetrakul, James R Ketudat-Cairns, Ratana Charoenwattanasatien, Voraratt Champattanachai, Chulaluck Kuptanon, Suthipong Pangkanon, Jisnuson Svasti
Clinical course, mutations and its functional characteristics of infantile-onset Pompe disease in Thailand. BMC medical genetics 20 (1) (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)

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Publication Activity (10 Years)

Top Topics

Top Venues

Duangrurdee Wattanasirichaigoon