Works by Chanin Limwongse

Results: 50

Thailand mutation and variation database (ThaiMUT).

Published in:

Human Mutation, 2008, v. 29, n. 8, p. E68, doi. 10.1002/humu.20787

By:

Ruangrit, Uttapong;
Srikummool, Metawee;
Assawamakin, Anunchai;
Ngamphiw, Chumpol;
Chuechote, Suparat;
Thaiprasarnsup, Vilasinee;
Agavatpanitch, Gallissara;
Pasomsab, Ekawat;
Yenchitsomanus, Pa-thai;
Mahasirimongkol, Surakameth;
Chantratita, Wasun;
Palittapongarnpim, Prasit;
Uyyanonvara, Bunyarit;
Limwongse, Chanin;
Tongsima, Sissades

Publication type:

Article

Association study identifies genetic determinants and non-genetic factors on steady-state plasma and therapeutic outcome of galantamine in mixed dementia.

Published in:

European Journal of Clinical Pharmacology, 2022, v. 78, n. 8, p. 1249, doi. 10.1007/s00228-022-03322-1

By:

Yaowaluk, Thitipon;
Senanarong, Vorapun;
Limwongse, Chanin;
Boonprasert, Rasda;
Bunditvorapoom, Duangkamon;
Kaewsutthi, Supannee;
Kijsanayotin, Pornpimol

Publication type:

Article

Influence of genetic and non-genetic factors on phenytoin-induced severe cutaneous adverse drug reactions.

Published in:

European Journal of Clinical Pharmacology, 2017, v. 73, n. 7, p. 855, doi. 10.1007/s00228-017-2250-2

By:

Yampayon, Kittika;
Sukasem, Chonlaphat;
Limwongse, Chanin;
Chinvarun, Yotin;
Tempark, Therdpong;
Rerkpattanapipat, Ticha;
Kijsanayotin, Pornpimol

Publication type:

Article

Novel Mutation of the TINF2 Gene in a Patient with Dyskeratosis Congenita.

Published in:

Case Reports in Dermatology, 2015, v. 7, n. 2, p. 212, doi. 10.1159/000439042

By:

Panichareon, Benjaporn;
Seedapan, Thanawat;
Thongnoppakhun, Wanna;
Limwongse, Chanin;
Pithukpakorn, Manop;
Limjindaporn, Thawornchai

Publication type:

Article

Glutathione S-transferase polymorphisms and risk of bladder cancer in Thais.

Published in:

Thai Journal of Pharmaceutical Sciences, 2009, v. 33, n. 2/3, p. 67

By:

Pradubkaew, Kannika;
Pramyothin, Pornpen;
Limwongse, Chanin;
Suwannasri, Payiarat;
Assawamakin, Anunchai

Publication type:

Article

Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome.

Published in:

Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 113, doi. 10.1002/(SICI)1098-2264(199802)21:2<113::AID-GCC6>3.0.CO;2-3

By:

Tsuchiya, Karen D.;
Wiesner, Georgia;
Cassidy, Suzanne B.;
Limwongse, Chanin;
Boyle, John T.;
Schwartz, Stuart

Publication type:

Article

Effect of gene polymorphisms in ADAM33, TGFβ1, VEGFA, and PLAUR on asthma in Thai population.

Published in:

Asian Pacific Journal of Allergy & Immunology, 2022, v. 40, n. 1, p. 39, doi. 10.12932/AP-010419-0532

By:

Thongngarm, Torpong;
Jameekornrak, Aree;
Chaiyaratana, Nachol;
Thongnoppakhun, Wanna;
Sangasapaviliya, Atik;
Jirapongsananuruk, Orathai;
Limwongse, Chanin

Publication type:

Article

How do we translate gaps and unmet needs of blood management for thalassemia into a collaborative implementation framework?

Published in:

Transfusion Medicine, 2023, v. 33, n. 6, p. 497, doi. 10.1111/tme.13011

By:

Limwongse, Chanin;
Rojnuckarin, Ponlapat;
Kupatawintu, Pawinee;
Thongthaisin, Aphisit;
Permpikul, Parichart;
Kitpoka, Pimpan;
Watanaboonyongcharoen, Phandee;
Sucharitchan, Pranee;
Torcharus, Kitti;
Fucharoen, Suthat;
Kongpakwattana, Khachen;
Nerapusee, Osot;
Chuncharunee, Suporn

Publication type:

Article

Skewed X chromosome inactivation in girls and female adolescents with autoimmune thyroid disease.

Published in:

Clinical Endocrinology, 2018, v. 89, n. 6, p. 863, doi. 10.1111/cen.13857

By:

Santiwatana, Suttikarn;
Mahachoklertwattana, Pat;
Limwongse, Chanin;
Khlairit, Patcharin;
Pongratanakul, Sarunyu;
Roothumnong, Ekkapong;
Prangphan, Kanjana;
Choubtum, Lulin;
Songdej, Duantida;
Poomthavorn, Preamrudee

Publication type:

Article

Mutation Analysis of the VMD2 Gene in Thai Families with Best Macular Dystrophy.

Published in:

Ophthalmic Genetics, 2008, v. 29, n. 3, p. 139, doi. 10.1080/13816810802087394

By:

Atchaneeyasakul, La-ongsri;
Jinda, Worapoj;
Sakolsatayadorn, Natta;
Trinavarat, Adisak;
Ruangvoravate, Ngamkae;
Thanasombatskul, Nualanong;
Thongnoppakhun, Wanna;
Limwongse, Chanin

Publication type:

Article

Novel and De-novo Truncating PAX6 Mutations and Ocular Phenotypes in Thai Aniridia Patients.

Published in:

Ophthalmic Genetics, 2006, v. 27, n. 1, p. 21, doi. 10.1080/13816810500481667

By:

Atchaneeyasakul, La-ongsri;
Trinavarat, Adisak;
Dulayajinda, Dhaivadee;
Kumpornsin, Kornphet;
Thongnoppakhun, Wanna;
Yenchitsomanus, Pa-thai;
Limwongse, Chanin

Publication type:

Article

Identification of a novel mutation in APP gene in a Thai subject with early-onset Alzheimer's disease.

Published in:

Neuropsychiatric Disease & Treatment, 2018, v. 14, p. 3015, doi. 10.2147/NDT.S180174

By:

Giau, Vo Van;
Senanarong, Vorapun;
Bagyinszky, Eva;
Limwongse, Chanin;
An, Seong Soo A;
Kim, SangYun

Publication type:

Article

Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 7, p. 1750, doi. 10.1002/ajmg.a.35422

By:

Kantaputra, Piranit Nik;
van den Ouweland, Ans;
Sangruchi, Tumtip;
Limwongse, Chanin

Publication type:

Article

A novel maternally-derived insertional translocation resulting in partial trisomy 4q13.2-q22.1 with complex translocation t(8;20) in a family with intellectual disability.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 4, p. 901, doi. 10.1002/ajmg.a.35259

By:

Assawamakin, Anunchai;
Wattanasirichaigoon, Duangrurdee;
Tocharoentanaphol, Chintana;
Waeteekul, Supaporn;
Tansatit, Montakarn;
Thongnoppakhun, Wanna;
Limwongse, Chanin

Publication type:

Article

Characteristics of β‐secretase activity on APP‐V604M and APP‐V669L.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 3, p. 1, doi. 10.1002/alz.064382

By:

Kim, Danyeong;
Shim, Kyu Hwan;
Bagyinszky, Eva;
Van Vo, Giau;
Kang, Min Ju;
Senanarong, Vorapun;
Limwongse, Chanin;
Shin, Seunghwan;
Jeong, SoonPyo;
Kim, Jongsung;
Park, Young Ho;
Youn, Young Chul;
Kim, SangYun;
An, Seong Soo

Publication type:

Article

P3‐099: A KNOWN PSEN1 E184G MUTATION IN AN EOAD PATIENT FROM THAILAND.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1105, doi. 10.1016/j.jalz.2018.06.1455

By:

Van Vo, Giau;
Bagyinszky, Eva;
Senanarong, Vorapun;
Limwongse, Chanin;
An, Seong Soo;
Kim, SangYun

Publication type:

Article

P1‐166: SCREENING FOR MUTATIONS IN EARLY‐ONSET ALZHEIMER'S DISEASE FROM THAILAND WITH ADAM GENEPANEL 1.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P342, doi. 10.1016/j.jalz.2018.06.170

By:

Van Vo, Giau;
Senanarong, Vorapun -;
Bagyinszky, Eva;
Limwongse, Chanin;
An, Seong Soo;
Kim, SangYun

Publication type:

Article

P1‐165: A NOVEL APP VAL604MET MUTATION IN A THAI WITH EARLY‐ONSET ALZHEIMER DISEASE.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P341, doi. 10.1016/j.jalz.2018.06.169

By:

Van Vo, Giau;
Senanarong, Vorapun;
Bagyinszky, Eva;
Limwongse, Chanin;
An, Seong Soo;
Kim, SangYun

Publication type:

Article

A novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosa.

Published in:

Molecular Vision, 2016, v. 22, p. 1

By:

Jinda, Worapoj;
Poungvarin, Naravat;
Taylor, Todd D.;
Yutaka Suzuki;
Thongnoppakhun, Wanna;
Limwongse, Chanin;
Lertrit, Patcharee;
Suriyaphol, Prapat;
Atchaneeyasakul, Laongsri

Publication type:

Article

Molecular and clinical characterization of Thai patients with achromatopsia: identification of three novel disease-associated variants in the CNGA3 and CNGB3 genes.

Published in:

International Ophthalmology, 2021, v. 41, n. 1, p. 121, doi. 10.1007/s10792-020-01559-2

By:

Jinda, Worapoj;
Tuekprakhon, Aekkachai;
Thongnoppakhun, Wanna;
Limwongse, Chanin;
Trinavarat, Adisak;
Atchaneeyasakul, La-ongsri

Publication type:

Article

Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand.

Published in:

Human Genetics, 2010, v. 128, n. 1, p. 39, doi. 10.1007/s00439-010-0821-8

By:

Phasukkijwatana, Nopasak;
Kunhapan, Bussaraporn;
Stankovich, Jim;
Chuenkongkaew, Wanicha L.;
Thomson, Russell;
Thornton, Timothy;
Bahlo, Melanie;
Mushiroda, Taisei;
Nakamura, Yusuke;
Mahasirimongkol, Surakameth;
Aung Win Tun;
Srisawat, Chatchawan;
Limwongse, Chanin;
Peerapittayamongkol, Chayanon;
Sura, Thanyachai;
Suthammarak, Wichit;
Lertrit, Patcharee

Publication type:

Article

Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia.

Published in:

Hematology, 2023, v. 28, n. 1, p. 1, doi. 10.1080/16078454.2023.2187155

By:

Hantaweepant, Chattree;
Suktitipat, Bhoom;
Pithukpakorn, Manop;
Chinthammitr, Yingyong;
Limwongse, Chanin;
Tansiri, Nawaporn;
Sawatnatee, Surasak;
Takpradit, Chayamon;
Rotchanapanya, Wannaphorn;
Pongudom, Saranya;
Charoenprasert, Kanyaporn;
Paiboonsukwong, Kittiphong;
Thamprasert, Wichuda;
Nolwachai, Narumol;
Rattanasawat, Wanlapa;
Sae-Aeng, Busakorn;
Khorwanichakij, Nisachon;
Saetow, Putchong;
Saengboon, Supawee;
Kamjornpreecha, Krittichat

Publication type:

Article

The efficacy of low-dose warfarin initiation (3 mg versus 5 mg) in newly diagnosed venous thromboembolism patients among a population with a high prevalence of warfarin-sensitive haplotype of the VKORC1 gene: a randomized controlled trial.

Published in:

Hematology, 2022, v. 27, n. 1, p. 95, doi. 10.1080/16078454.2021.2019891

By:

Suwanawiboon, Bundarika;
Rotchanapanya, Wannaphorn;
Mahaprom, Komkrit;
Thongnoppakhun, Wanna;
Lalerd, Yupaporn;
Limwongse, Chanin;
Sermsathanasawadi, Nuttawut;
Owattanapanich, Weerapat

Publication type:

Article

Familial clustering of nonalcoholic fatty liver disease in first‐degree relatives of adults with lean nonalcoholic fatty liver disease.

Published in:

Liver International, 2023, v. 43, n. 12, p. 2713, doi. 10.1111/liv.15758

By:

Niltwat, Sorachat;
Limwongse, Chanin;
Charatcharoenwitthaya, Natthinee;
Bunditvorapoom, Duangkamon;
Bandidniyamanon, Wimolrak;
Charatcharoenwitthaya, Phunchai

Publication type:

Article

Association of Oxcarbazepine-induced Cutaneous Adverse Drug Reactions with HLA-B*15:02 Allele.

Published in:

Siriraj Medical Journal, 2020, v. 72, n. 2, p. 174, doi. 10.33192/Smj.2020.23

By:

Pramote Euasobhon;
Sukunya Jirachaipitak;
Suwanna Chanpradub;
Pranee Rushatamukayanunt;
Chanin Limwongse;
Courtney, Peter

Publication type:

Article

Tumor mutational profile of triple negative breast cancer patients in Thailand revealed distinctive genetic alteration in chromatin remodeling gene.

Published in:

PeerJ, 2019, p. 1, doi. 10.7717/peerj.6501

By:

Niyomnaitham, Suvimol;
Parinyanitikul, Napa;
Roothumnong, Ekkapong;
Jinda, Worapoj;
Samarnthai, Norasate;
Atikankul, Taywin;
Suktitipat, Bhoom;
Thongnoppakhun, Wanna;
Limwongse, Chanin;
Pithukpakorn, Manop

Publication type:

Article

Identification of novel mutation in RANKL by whole‐exome sequencing in a Thai family with osteopetrosis; a case report and review of RANKL osteopetrosis.

Published in:

Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 7, p. 1, doi. 10.1002/mgg3.1727

By:

Lertwilaiwittaya, Pongtawat;
Suktitipat, Bhoom;
Khongthon, Phongphak;
Pongsapich, Warut;
Limwongse, Chanin;
Pithukpakorn, Manop

Publication type:

Article

Genetics and genomics in Thailand: challenges and opportunities.

Published in:

Molecular Genetics & Genomic Medicine, 2014, v. 2, n. 3, p. 210, doi. 10.1002/mgg3.83

By:

Shotelersuk, Vorasuk;
Limwongse, Chanin;
Mahasirimongkol, Surakameth

Publication type:

Article

A NovelMutation of the GNE Gene in Distal Myopathy with Rimmed Vacuoles: A Case with Inflammation.

Published in:

Case Reports in Neurology, 2014, v. 6, n. 1, p. 55, doi. 10.1159/000360730

By:

Tanboon, Jantima;
Rongsa, Kanjana;
Pithukpakorn, Manop;
Boonyapisit, Kanokwan;
Limwongse, Chanin;
Sangruchi, Tumtip

Publication type:

Article

Orientia tsutsugamushi Stimulates an Original Gene Expression Program in Monocytes: Relationship with Gene Expression in Patients with Scrub Typhus.

Published in:

PLoS Neglected Tropical Diseases, 2011, v. 5, n. 5, p. 1, doi. 10.1371/journal.pntd.0001028

By:

Tantibhedhyangkul, Wiwit;
Prachason, Thanavadee;
Waywa, Duangdao;
El Filali, Adil;
Ghigo, Eric;
Thongnoppakhun, Wanna;
Raoult, Didier;
Suputtamongkol, Yupin;
Capo, Christian;
Limwongse, Chanin;
Mege, Jean-Louis

Publication type:

Article

Orientia tsutsugamushi Stimulates an Original Gene Expression Program in Monocytes: Relationship with Gene Expression in Patients with Scrub Typhus.

Published in:

PLoS Neglected Tropical Diseases, 2011, v. 5, n. 5, p. 1, doi. 10.1371/journal.pntd.0001028

By:

Tantibhedhyangkul, Wiwit;
Prachason, Thanavadee;
Waywa, Duangdao;
Filali, Adil El;
Ghigo, Eric;
Thongnoppakhun, Wanna;
Raoult, Didier;
Suputtamongkol, Yupin;
Capo, Christian;
Limwongse, Chanin;
Mege, Jean-Louis

Publication type:

Article

Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome presenting with a large nephrogenic cyst, severe oligohydramnios and hydrops fetalis: a case report and review of the literature.

Published in:

2005

By:

Chuangsuwanich, Tuenjai;
Sunsaneevithayakul, Prasert;
Muangsomboon, Kobkun;
Limwongse, Chanin

Publication type:

journal article

Prevalence and implications of fragile X premutation screening in Thailand.

Published in:

Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-77762-3

By:

Hnoonual, Areerat;
Kaewfai, Sunita;
Limwongse, Chanin;
Limprasert, Pornprot

Publication type:

Article

Influence of CYP2D6, CYP3A5, ABCB1, APOE polymorphisms and nongenetic factors on donepezil treatment in patients with Alzheimer's disease and vascular dementia.

Published in:

Pharmacogenomics & Personalized Medicine, 2019, v. 12, p. 209, doi. 10.2147/PGPM.S211259

By:

Yaowaluk, Thitipon;
Senanarong, Vorapun;
Limwongse, Chanin;
Boonprasert, Rasda;
Kijsanayotin, Pornpimol

Publication type:

Article

A Novel Mutation in the β-Subunit of the Epithelial Sodium Channel Gene (SCNN1B) in a Thai Family with Liddle's Syndrome.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2009, v. 22, n. 1, p. 85

By:

Palrunyar Sawathlparntch;
Achra Sumboonnanonda;
Praewwarin Weerakulwattana;
Chanin Limwongse

Publication type:

Article

Single-Tube Screen for Rapid Detection of Repeat Expansions in Seven Common Spinocerebellar Ataxias.

Published in:

Clinical Chemistry, 2022, v. 68, n. 6, p. 794, doi. 10.1093/clinchem/hvac011

By:

Mulias Lian;
Chanin Limwongse;
Chui-Sheun Yoon;
Lee, Caroline G.;
Hai-Yang Law;
Chong, Samuel S.

Publication type:

Article

Alleviated bleeding phenotypes in a child with severe haemophilia A and thalassemia disease.

Published in:

Haemophilia, 2024, v. 30, n. 4, p. 1092, doi. 10.1111/hae.15041

By:

Pongphitcha, Pongpak;
Sasanakul, Werasak;
Kadegasem, Praguywan;
Songdej, Duantida;
Limwongse, Chanin;
Amesbutr, Mattana;
Jaovisidha, Suphaneewan;
Chuansumrit, Ampaiwan;
Sirachainan, Nongnuch

Publication type:

Article

Problems in determining thalassemia carrier status in a program for prevention and control of severe thalassemia syndromes: a lesson from Thailand.

Published in:

Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 8, p. 1605, doi. 10.1515/cclm-2013-0098

By:

Vip Viprakasit;
Chanin Limwongse;
Sathein Sukpanichnant;
Pornpimol Ruangvutilert;
Chompunut Kanjanakorn;
Waraporn Glomglao;
Monchan Sirikong;
Witayakarn Utto;
Voravarn S. Tanphaichitr

Publication type:

Article

EFFECTS OF PCSK1 GENETIC VARIANTS ON OBESITY AMONG THAI CHILDREN AND THEIR FAMILY MEMBERS: IN RELATION TO HEALTH RISK, AND BIOCHEMICAL AND ANTHROPOMETRIC PARAMETERS.

Published in:

Southeast Asian Journal of Tropical Medicine & Public Health, 2014, v. 45, n. 1, p. 214

By:

Sirikul Kulanuwat;
Benjaluck Phonrat;
Anchalee Tungtrongchitr;
Chanin Limwongse;
Nalinee Chongviriyaphan;
Rungsunn Tungtrongchitr;
Jeerunda Santiprabhob

Publication type:

Article

Hemoglobin Pakse: presence on red blood cell membrane and detection by polymerase chain reaction-single-strand conformational polymorphism.

Published in:

2004

By:

Turbpaiboon, Chairat;
Siritantikorn, Atchasai;
Thongnoppakhun, Wanna;
Bunditworapoom, Duangkamon;
Limwongse, Chanin;
Yenchitsomanus, Pa-thai;
Siritanaratkul, Noppadol;
Wilairat, Prapon

Publication type:

journal article

Activation of Indoleamine 2,3-Dioxygenase in Patients with Scrub Typhus and Its Role in Growth Restriction of Orientia tsutsugamushi.

Published in:

PLoS Neglected Tropical Diseases, 2012, v. 6, n. 7, p. 1, doi. 10.1371/journal.pntd.0001731

By:

Prachason, Thanavadee;
Konhan, Kanittha;
Pongnarin, Piyapat;
Chatsiricharoenkul, Somruedee;
Suputtamongkol, Yupin;
Limwongse, Chanin

Publication type:

Article

Activation of Indoleamine 2,3-Dioxygenase in Patients with Scrub Typhus and Its Role in Growth Restriction of Orientia tsutsugamushi.

Published in:

PLoS Neglected Tropical Diseases, 2012, v. 6, n. 7, p. 1, doi. 10.1371/journal.pntd.0001731

By:

Prachason, Thanavadee;
Konhan, Kanittha;
Pongnarin, Piyapat;
Chatsiricharoenkul, Somruedee;
Suputtamongkol, Yupin;
Limwongse, Chanin

Publication type:

Article

Gene Distribution in Pediatric-Onset Inherited Peripheral Neuropathy: A Single Tertiary Center in Thailand.

Published in:

Journal of Neuromuscular Diseases, 2024, v. 11, n. 1, p. 191, doi. 10.3233/JND-230174

By:

Kulsirichawaroj, Pimchanok;
Suksangkharn, Yanin;
Nam, Da Eun;
Pho-iam, Theeraphong;
Limwongse, Chanin;
Chung, Ki Wha;
Sanmaneechai, Oranee;
Zuchner, Stephan L.;
Choi, Byung-Ok

Publication type:

Article

Mutations in the XLRS1 gene in Thai families with X-linked juvenile retinoschisis.

Published in:

Japanese Journal of Ophthalmology, 2010, v. 54, n. 1, p. 89, doi. 10.1007/s10384-009-0748-6

By:

Atchaneeyasakul, La-ongsri;
Trinavarat, Adisak;
Pituksung, Auengporn;
Jinda, Worapoj;
Thongnoppakhun, Wanna;
Limwongse, Chanin

Publication type:

Article

Etiology of Dementia in Thai Patients.

Published in:

Dementia & Geriatric Cognitive Disorders Extra, 2021, v. 11, n. 1, p. 64, doi. 10.1159/000515676

By:

Dharmasaroja, Pornpatr A.;
Assanasen, Jintana;
Pongpakdee, Sunsanee;
Jaisin, Kankamol;
Lolekha, Praween;
Phanasathit, Muthita;
Cheewakriengkrai, Laksanun;
Chotipanich, Chanisa;
Witoonpanich, Pirada;
Pitiyarn, Sutisa;
Lertwilaiwittaya, Pongtawat;
Dejthevaporn, Charungthai;
Limwongse, Chanin;
Phanthumchinda, Kammant

Publication type:

Article

Association between ADAM33 Polymorphisms and Asthma in a Thai Population.

Published in:

Asian Pacific Journal of Allergy & Immunology, 2008, v. 26, n. 4, p. 205

By:

Thongngarm, Torpong;
Jameekornrak, Aree;
Limwongse, Chanin;
Sangasapaviliya, Atik;
Jirapongsananuruk, Orathai;
Assawamakin, Anunchai;
Chaiyaratana, Nachol;
Luangwedchakarn, Voravich;
Thongnoppakhun, Wanna

Publication type:

Article

Thai patients who fulfilled NCCN criteria for breast/ovarian cancer genetic assessment demonstrated high prevalence of germline mutations in cancer susceptibility genes: implication to Asian population testing.

Published in:

Breast Cancer Research & Treatment, 2021, v. 188, n. 1, p. 237, doi. 10.1007/s10549-021-06152-4

By:

Lertwilaiwittaya, Pongtawat;
Roothumnong, Ekkapong;
Nakthong, Panee;
Dungort, Peerawat;
Meesamarnpong, Chutima;
Tansa-Nga, Warisara;
Pongsuktavorn, Khontawan;
Wiboonthanasarn, Supakit;
Tititumjariya, Warunya;
Thongnoppakhun, Wanna;
Chanprasert, Sirisak;
Limwongse, Chanin;
Pithukpakorn, Manop

Publication type:

Article

Germline mutations of 4567 patients with hereditary breast-ovarian cancer spectrum in Thailand.

Published in:

NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00400-4

By:

Kansuttiviwat, Chalermkiat;
Lertwilaiwittaya, Pongtawat;
Roothumnong, Ekkapong;
Nakthong, Panee;
Dungort, Peerawat;
Meesamarnpong, Chutima;
Tansa-Nga, Warisara;
Pongsuktavorn, Khontawan;
Wiboonthanasarn, Supakit;
Tititumjariya, Warunya;
Phuphuripan, Nannipa;
Lertbussarakam, Chittapat;
Wattanarangsan, Jantanee;
Sritun, Jiraporn;
Punuch, Kittiporn;
Kammarabutr, Jirayu;
Mutirangura, Pornthira;
Thongnoppakhun, Wanna;
Limwongse, Chanin;
Pithukpakorn, Manop

Publication type:

Article

Germline mutations of 4567 patients with hereditary breast-ovarian cancer spectrum in Thailand.

Published in:

NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00400-4

By:

Kansuttiviwat, Chalermkiat;
Lertwilaiwittaya, Pongtawat;
Roothumnong, Ekkapong;
Nakthong, Panee;
Dungort, Peerawat;
Meesamarnpong, Chutima;
Tansa-Nga, Warisara;
Pongsuktavorn, Khontawan;
Wiboonthanasarn, Supakit;
Tititumjariya, Warunya;
Phuphuripan, Nannipa;
Lertbussarakam, Chittapat;
Wattanarangsan, Jantanee;
Sritun, Jiraporn;
Punuch, Kittiporn;
Kammarabutr, Jirayu;
Mutirangura, Pornthira;
Thongnoppakhun, Wanna;
Limwongse, Chanin;
Pithukpakorn, Manop

Publication type:

Article

Novel and de novo PKD1 mutations identified by multiple restriction fragment-single strand conformation polymorphism (MRF-SSCP).

Published in:

BMC Medical Genetics, 2004, v. 5, p. 1

By:

Wanna Thongnoppakhun;
Chanin Limwongse;
Kriengsak Vareesangthip;
Chintana Sirinavin;
Duangkamon Bunditworapoom;
Nanyawan Rungroj;
Pa-thai Yenchitsomanus

Publication type:

Article