Vorasuk Shotelersuk

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 28

Top Venues

Clinical genetics

American journal of medical genetics. Part A

Oral diseases

European journal of human genetics : EJHG

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

Publications

Narin Intarak, Chawan Manaspon, Thanakorn Theerapanon, Sasiprapa Prommanee, Lakshman Perera Samaranayake, Vorasuk Shotelersuk, Thantrira Porntaveetus
Tooth agenesis related to a novel KDF1 variant: A case report and literature review. Oral diseases (2024)
Elena Ambrosino, Ahmad N Abou Tayoun, Marc Abramowicz, Bin Alwi Zilfalil, Tiffany F Boughtwood, Yosr Hamdi, Tim Hubbard, Kazuto Kato, Iscia Lopes-Cendes, Partha Pratim Majumder, Deborah Mascalzoni, Rokhaya Ndiaye, Michelle Ramsay, Gabriela M Repetto, Vorasuk Shotelersuk, Sherry Taylor, John C Reeder, Anna Laura Ross
The WHO genomics program of work for equitable implementation of human genomics for global health. Nature medicine (2024)
Patra Yeetong, Mohamed E Dembélé, Monnat Pongpanich, Lassana Cissé, Chalurmpon Srichomthong, Alassane B Maiga, Kékouta Dembélé, Adjima Assawapitaksakul, Salia Bamba, Abdoulaye Yalcouyé, Salimata Diarra, Samuel Ephrata Mefoung, Supphakorn Rakwongkhachon, Oumou Traoré, Siraprapa Tongkobpetch, Kenneth H Fischbeck, William A Gahl, Cheick O Guinto, Vorasuk Shotelersuk, Guida Landouré
Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8. Movement disorders : official journal of the Movement Disorder Society (2023)
Rauan Kaiyrzhanov, Aboulfazl Rad, Sheng-Jia Lin, Aida Bertoli-Avella, Wouter W Kallemeijn, Annie Godwin, Maha S Zaki, Kevin Huang, Tracy Lau, Cassidy Petree, Stephanie Efthymiou, Ehsan Ghayoor Karimiani, Maja Hempel, Elizabeth A Normand, Sabine Rudnik-Schöneborn, Ulrich A Schatz, Marc P Baggelaar, Muhammad Ilyas, Tipu Sultan, Javeria Raza Alvi, Manizha Ganieva, Ben Fowler, Ruxandra Aanicai, Gulsen Akay Tayfun, Abdulaziz Al Saman, Abdulrahman Alswaid, Nafise Amiri, Nilufar Asilova, Vorasuk Shotelersuk, Patra Yeetong, Matloob Azam, Meisam Babaei, Gholamreza Bahrami Monajemi, Pouria Mohammadi, Saeed Samie, Selina Husna Banu, Jorge Pinto Basto, Fanny Kortüm, Mislen Bauer, Peter Bauer, Christian Beetz, Masoud Garshasbi, Awatif Hameed Issa, Wafaa Eyaid, Hind Ahmed, Narges Hashemi, Kazem Hassanpour, Isabella Herman, Sherozjon Ibrohimov, Ban A Abdul-Majeed, Maria Imdad, Maksudjon Isrofilov, Qassem Kaiyal, Suliman Khan, Brian Kirmse, Janet Koster, Charles Marques Lourenço, Tadahiro Mitani, Oana Moldovan, David Murphy, Maryam Najafi, Davut Pehlivan, Maria Eugenia Rocha, Vincenzo Salpietro, Miriam Schmidts, Adel Shalata, Mohammad Mahroum, Jawabreh Kassem Talbeya, Robert W Taylor, Dayana Vazquez, Annalisa Vetro, Hans R Waterham, Mashaya Zaman, Tina A Schrader, Wendy K Chung, Renzo Guerrini, James R Lupski, Joseph Gleeson, Mohnish Suri, Yalda Jamshidi, Kailash P Bhatia, Barbara Vona, Michael Schrader, Mariasavina Severino, Matthew Guille, Edward W Tate, Guarav K Varshney, Henry Houlden, Reza Maroofian
Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders. Brain : a journal of neurology (2023)
Sirivipa Piyamongkol, Krit Makonkawkeyoon, Vorasuk Shotelersuk, Opas Sreshthaputra, Tawiwan Pantasri, Rekwan Sittiwangkul, Theera Tongsong, Wirawit Piyamongkol
Pre-implantation genetic testing for Marfan syndrome using mini-sequencing. Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology (2022)
Nithiphut Tantirukdham, Taninee Sahakitrungruang, Ratikorn Chaisiwamongkol, Monnat Pongpanich, Chalurmpon Srichomthong, Adjima Assawapitaksakul, Aayalida Buasong, Siraprapa Tongkobpetch, Patra Yeetong, Vorasuk Shotelersuk
Long-read Amplicon Sequencing of the CYP21A2 in 48 Thai Patients With Steroid 21-Hydroxylase Deficiency. The Journal of clinical endocrinology and metabolism 107 (7) (2022)
Ranchana Yeewa, Pawita Chaiya, Salinee Jantrapirom, Vorasuk Shotelersuk, Luca Lo Piccolo
Multifaceted roles of YEATS domain-containing proteins and novel links to neurological diseases. Cellular and molecular life sciences : CMLS 79 (3) (2022)
Monpat Chamnanphon, Monnat Pongpanich, Thitima Benjachat Suttichet, Watsamon Jantarabenjakul, Pattama Torvorapanit, Opass Putcharoen, Pimpayao Sodsai, Chureerat Phokaew, Nattiya Hirankarn, Pajaree Chariyavilaskul, Vorasuk Shotelersuk
Host genetic factors of COVID-19 susceptibility and disease severity in a Thai population. Journal of human genetics 67 (5) (2022)
Thivaratana Sinthuwiwat, Supranee Buranapraditkun, Wuttichart Kamolvisit, Siraprapa Tongkobpetch, Wanna Chetruengchai, Chalurmpon Srichomthong, Adjima Assawapitaksakul, Chureerat Phokaew, Patipark Kueanjinda, Tanapat Palaga, Tadech Boonpiyathad, Kanya Suphapeetiporn, Nattiya Hirankarn, Vorasuk Shotelersuk
A LILRB1 variant with a decreased ability to phosphorylate SHP-1 leads to autoimmune diseases. Scientific reports 12 (1) (2022)
Khanti Rattanapornsompong, Patcharaporn Gavila, Somkanya Tungsanga, Ankanee Chanakul, Atitaya Apivatthakakul, Maliwan Tengsujaritkul, Theera Tongsong, Thanakorn Theerapanon, Thantrira Porntaveetus, Vorasuk Shotelersuk
Novel CNNM4 variant and clinical features of Jalili syndrome. Clinical genetics (2022)
Guillaume Butler-Laporte, Gundula Povysil, Jack A Kosmicki, Elizabeth T Cirulli, Theodore G Drivas, Simone Furini, Chadi Saad, Axel Schmidt, Pawel Olszewski, Urszula Korotko, Mathieu Quinodoz, Elifnaz Celik, Kousik Kundu, Klaudia Walter, Junghyun Jung, Amy D Stockwell, Laura G Sloofman G Sloofman, Daniel M Jordan, Ryan C Thompson, Diane M Del Valle, Nicole W Simons, Esther Cheng, Robert Sebra, Eric E Schadt, Seunghee Kim-Schulze, Sacha Gnjatic, Miriam Merad, Joseph D Buxbaum, Noam D Beckmann, Alexander W Charney, Bartlomiej Przychodzen, Timothy S Chang, Tess D Pottinger, Ning Shang, Fabian Brand, Francesca Fava, Francesca Mari, Karolina Chwialkowska, Magdalena Niemira, Szymon Pula, J Kenneth Baillie, Alex Stuckey, Antonio Salas, Xabier Bello, Jacobo Pardo-Seco, Alberto Gómez-Carballa, Irene Rivero-Calle, Federico Martinón-Torres, Andrea Ganna, Konrad J Karczewski, Kumar Veerapen, Mathieu Bourgey, Guillaume Bourque, Robert Jm Eveleigh, Vincenzo Forgetta, David R Morrison, David Langlais, Mark Lathrop, Vincent Mooser, Tomoko Nakanishi, Robert Frithiof, Michael Hultström, Miklos Lipcsey, Yanara Marincevic-Zuniga, Jessica Nordlund, Kelly M Schiabor Barrett, William Lee, Alexandre Bolze, Simon White, Stephen Riffle, Francisco Tanudjaja, Efren Sandoval, Iva Neveux, Shaun Dabe, Nicolas Casadei, Susanne Motameny, Manal Alaamery, Salam Massadeh, Nora Aljawini, Mansour S Almutairi, Yaseen M Arabi, Saleh A Alqahtani, Fawz S Al Harthi, Amal Almutairi, Fatima Alqubaishi, Sarah Alotaibi, Albandari Binowayn, Ebtehal A Alsolm, Hadeel El Bardisy, Mohammad Fawzy, Fang Cai, Nicole Soranzo, Adam Butterworth, null null, null null, null null, null null, null null, null null, null null, null null, Daniel H Geschwind, Stephanie A Arteaga, Alexis Stephens, Manish J Butte, Paul C Boutros, Takafumi N Yamaguchi, Shu Tao, Stefan E Eng, Timothy Sanders, Paul J Tung, Michael E Broudy, Yu Pan, Alfredo E Gonzalez, Nikhil Chavan, Ruth Johnson, Bogdan Pasaniuc, Brian L Yaspan, Christos M Polymeropoulos, Carlo Rivolta, Stephanie Bibert, Pierre-Yves Bochud, Maciej Dąbrowski, Pawel Zawadzki, Mateusz Sypniewski, Elżbieta Kaja, Pajaree Chariyavilaskul, Voraphoj Nilaratanakul, Nattiya Hirankarn, Vorasuk Shotelersuk, Monnat Pongpanich, Chureerat Phokaew, Wanna Chetruengchai, Katsushi Tokunaga, Masaya Sugiyama, Yosuke Kawai, Takanori Hasegawa, Tatsuhiko Naito, Ho Namkoong, Ryuya Edahiro, Akinori Kimura, Seishi Ogawa, Takanori Kanai, Koichi Fukunaga, Yukinori Okada, Seiya Imoto, Satoru Miyano, Serghei Mangul, Malak S Abedalthagafi, Hugo Zeberg, Joseph J Grzymski, Nicole L Washington, Stephan Ossowski, Kerstin U Ludwig, Eva C Schulte, Olaf Riess, Marcin Moniuszko, Miroslaw Kwasniewski, Hamdi Mbarek, Said I Ismail, Anurag Verma, David B Goldstein, Krzysztof Kiryluk, Alessandra Renieri, Manuel A R Ferreira, John Brent Richards
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. PLoS genetics 18 (11) (2022)
Karn Wejaphikul, Khomsak Srilanchakon, Wuttichart Kamolvisit, Supavadee Jantasuwan, Kanokwan Santawong, Siraprapa Tongkobpetch, Thanakorn Theerapanon, Alisara Damrongmanee, Nattaphorn Hongsawong, Nuthapong Ukarapol, Prapai Dejkhamron, Vichit Supornsilchai, Thantrira Porntaveetus, Vorasuk Shotelersuk
Novel variants and phenotypes in NEUROG3 associated syndrome. The Journal of clinical endocrinology and metabolism (2022)
Narin Intarak, Thanakorn Theerapanon, Thantrira Porntaveetus, Vorasuk Shotelersuk
Patterns of molar agenesis associated with p.P20L and p.R77Q variants in PAX9. European journal of oral sciences 130 (2) (2022)
Chulaluck Kuptanon, Verasak Thamkunanon, Chalurmpon Srichomthong, Thanakorn Theerapanon, Kanya Suphapeetiporn, Thantrira Porntaveetus, Vorasuk Shotelersuk
Novel BMP1, CRTAP, and SERPINF1 variants causing autosomal recessive osteogenesis imperfecta. Clinical genetics 102 (3) (2022)
Ponghatai Boonsimma, Chupong Ittiwut, Wuttichart Kamolvisit, Rungnapa Ittiwut, Wanna Chetruengchai, Chureerat Phokaew, Chalurmpon Srichonthong, Sathida Poonmaksatit, Tayard Desudchit, Kanya Suphapeetiporn, Vorasuk Shotelersuk
Exome sequencing as first-tier genetic testing in infantile-onset pharmacoresistant epilepsy: diagnostic yield and treatment impact. European journal of human genetics : EJHG (2022)
Kanokwan Sriwattanapong, Noppadol Sa-Ard-Iam, Lawan Boonprakong, Keskanya Subbalekha, Vorapat Trachoo, Narissara Suratannon, Thantrira Porntaveetus, Vorasuk Shotelersuk
Reduced ELANE and SLPI expression compromises dental pulp cell activity. Cell proliferation 54 (11) (2021)
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)
Maliwan Tengsujaritkul, Narissara Suratannon, Chupong Ittiwut, Rungnapa Ittiwut, Pantipa Chatchatee, Kanya Suphapeetiporn, Vorasuk Shotelersuk
Phenotypic heterogeneity and genotypic spectrum of inborn errors of immunity identified through whole exome sequencing in a Thai patient cohort. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology (2021)
Vorasuk Shotelersuk, Duangdao Wichadakul, Chumpol Ngamphiw, Chalurmpon Srichomthong, Chureerat Phokaew, Alisa Wilantho, Sujiraporn Pakchuen, Vorthunju Nakhonsri, Philip James Shaw, Rujipat Wasitthankasem, Jittima Piriyapongsa, Pongsakorn Wangkumhang, Adjima Assawapitaksakul, Wanna Chetruengchai, Keswadee Lapphra, Athiphat Khuninthong, Pattarapong Makarawate, Kanya Suphapeetiporn, Surakameth Mahasirimongkol, Nusara Satproedprai, Thantrira Porntaveetus, Prapaporn Pisitkun, Verayuth Praphanphoj, Piranit Nik Kantaputra, Wichittra Tassaneeyakul, Sissades Tongsima
The Thai reference exome (T-REx) variant database. Clinical genetics 100 (6) (2021)
Wanna Chetruengchai, Vorasuk Shotelersuk
Actionable secondary findings in the 73 ACMG-recommended genes in 1559 Thai exomes. Journal of human genetics (2021)
Chawan Manaspon, Ponghatai Boonsimma, Chureerat Phokaew, Thanakorn Theerapanon, Kanokwan Sriwattanapong, Thantrira Porntaveetus, Vorasuk Shotelersuk
Expanding the genotypic spectrum of PYCR2 and a common ancestry in Thai patients with hypomyelinating leukodystrophy 10. American journal of medical genetics. Part A 185 (10) (2021)
Kuntharee Traisrisilp, Wisit Chankhunaphas, Rekwan Sittiwangkul, Chureerat Phokaew, Vorasuk Shotelersuk, Theera Tongsong
Prenatal Sonographic Features of CHARGE Syndrome. Diagnostics (Basel, Switzerland) 11 (3) (2021)
Narin Intarak, Thunyaporn Budsamongkol, Thanakorn Theerapanon, Theerapat Chanamuangkon, Anucharte Srijunbarl, Lawan Boonprakong, Thantrira Porntaveetus, Vorasuk Shotelersuk
Tooth ultrastructure of a novel COL1A2 mutation expanding its genotypic and phenotypic spectra. Oral diseases 27 (5) (2020)
Patra Yeetong, Chaipat Chunharas, Monnat Pongpanich, Mark F Bennett, Chalurmpon Srichomthong, Nath Pasutharnchat, Kanya Suphapeetiporn, Melanie Bahlo, Vorasuk Shotelersuk
Founder effect of the TTTCA repeat insertions in SAMD12 causing BAFME1. European journal of human genetics : EJHG 29 (2) (2020)
Vorasuk Shotelersuk, Sissades Tongsima, Manop Pithukpakorn, Jakris Eu-Ahsunthornwattana, Surakameth Mahasirimongkol
Precision medicine in Thailand. American journal of medical genetics. Part C, Seminars in medical genetics 181 (2) (2019)
Narin Intarak, Thanakorn Theerapanon, Sermporn Thaweesapphithak, Kanya Suphapeetiporn, Thantrira Porntaveetus, Vorasuk Shotelersuk
Genotype-phenotype correlation and expansion of orodental anomalies in LTBP3-related disorders. Molecular genetics and genomics : MGG 294 (3) (2019)
Thantrira Porntaveetus, Thanakorn Theerapanon, Chalurmpon Srichomthong, Vorasuk Shotelersuk
Cole-Carpenter syndrome in a patient from Thailand. American journal of medical genetics. Part A 176 (8) (2018)
Uschi Lindert, Wayne A Cabral, Surasawadee Ausavarat, Siraprapa Tongkobpetch, Katja Ludin, Aileen M Barnes, Patra Yeetong, Maryann Weis, Birgit Krabichler, Chalurmpon Srichomthong, Elena N Makareeva, Andreas R Janecke, Sergey Leikin, Benno Röthlisberger, Marianne Rohrbach, Ingo Kennerknecht, David R Eyre, Kanya Suphapeetiporn, Cecilia Giunta, Joan C Marini, Vorasuk Shotelersuk
MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta. Nature communications 7 (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Vorasuk Shotelersuk