Wanna Thongnoppakhun

Wanna Thongnoppakhun

Mahidol University

H-index: 21

Asia-Thailand

About Wanna Thongnoppakhun

Wanna Thongnoppakhun, With an exceptional h-index of 21 and a recent h-index of 12 (since 2020), a distinguished researcher at Mahidol University, specializes in the field of human molecular genetics.

His recent articles reflect a diverse array of research interests and contributions to the field:

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

Genomic alteration in sporadic adolescent and young adult-onset colorectal adenocarcinoma.

P069: Clinical and genomic spectrum of Lynch syndrome in Thailand: A 7-year experience of cancer genetic testing at Siriraj Genomics

Germline mutations in hereditary breast-ovarian cancer spectrum in Thailand: Results from multi-gene panel testing in 4,567 Thai patients

STK11 Causative Variants and Copy Number Variations Identified in Thai Patients With Peutz-Jeghers Syndrome

PRRT2 Gene Analysis of Paroxysmal Kinesigenic Dyskinesia (PKD) in Thai Children

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

Genetic Analysis of Children with Dravet Syndrome in a Resource-limited Setting

Wanna Thongnoppakhun Information

University

Position

Lecturer Research Department

Citations(all)

1760

Citations(since 2020)

702

Cited By

1314

hIndex(all)

21

hIndex(since 2020)

12

i10Index(all)

41

i10Index(since 2020)

18

Email

University Profile Page

Mahidol University

Google Scholar

View Google Scholar Profile

Wanna Thongnoppakhun Skills & Research Interests

human molecular genetics

Top articles of Wanna Thongnoppakhun

Title

Journal

Author(s)

Publication Date

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

npj Genomic Medicine

Chalermkiat Kansuttiviwat

Pongtawat Lertwilaiwittaya

Ekkapong Roothumnong

Panee Nakthong

Peerawat Dungort

...

2024/2/14

Genomic alteration in sporadic adolescent and young adult-onset colorectal adenocarcinoma.

Krittiya Korphaisarn

Phuwanat Sakornsakolpat

Ananya Pongpaibul

Ekkapong Roothumnong

Wanna Thongnoppakhun

...

2024/1/20

P069: Clinical and genomic spectrum of Lynch syndrome in Thailand: A 7-year experience of cancer genetic testing at Siriraj Genomics

Genetics in Medicine Open

Chalermkiat Kansuttiviwat

Pongtawat Lertwilaiwittaya

Ekkapong Roothumnong

Panee Nakthong

Peerawat Dungort

...

2024/1/1

Germline mutations in hereditary breast-ovarian cancer spectrum in Thailand: Results from multi-gene panel testing in 4,567 Thai patients

Manop Pithukpakorn

Chalermkiat Kansuttiviwat

Pongtawat Lertwilaiwittaya

Ekkapong Roothumnong

Panee Nakthong

...

2023/9/28

STK11 Causative Variants and Copy Number Variations Identified in Thai Patients With Peutz-Jeghers Syndrome

Cureus

Wannasiri Chiraphapphaiboon

Wanna Thongnoppakhun

Thawornchai Limjindaporn

Sunisa Sawasdichai

Ekkapong Roothumnong

...

2023/2/1

PRRT2 Gene Analysis of Paroxysmal Kinesigenic Dyskinesia (PKD) in Thai Children

Journal of Health Science and Medical Research

Pantaree Laosuebsakulthai

Surachai Likasitwattanakul

Theerapong Pho-Iam

Wanna Thongnoppakhun

Mongkol Chanvanichtrakool

2022/5/4

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

Asian Pacific Journal of Allergy and Immunology

Torpong Thongngarm

Aree Jameekornrak

Nachol Chaiyaratana

Wanna Thongnoppakhun

Atik Sangasapaviliya

...

2022/3/1

Genetic Analysis of Children with Dravet Syndrome in a Resource-limited Setting

Journal of Health Science and Medical Research

Sorawit Viravan

Chutima Meesamarnpong

Wanna Thongnoppakhun

Mongkol Chanvanichtrakool

2022/2/23

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 …

Hematology

Bundarika Suwanawiboon

Wannaphorn Rotchanapanya

Komkrit Mahaprom

Wanna Thongnoppakhun

Yupaporn Lalerd

...

2022/12/31

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

International Ophthalmology

Worapoj Jinda

Aekkachai Tuekprakhon

Wanna Thongnoppakhun

Chanin Limwongse

Adisak Trinavarat

...

2021/1

Identification of a novel TSC2 pathogenic frameshift insertion causing tuberous sclerosis complex, an inherited tumor syndrome in a sporadic case

Genomics and Genetics

Punyaapa Srikirin

Thawornchai Limjindaporn

Chanin Limwongse

Manop Pithukpakorn

Ekkapong Roothumnong

...

2021/7/3

Thai patients who fulfilled NCCN criteria for breast/ovarian cancer genetic assessment demonstrated high prevalence of germline mutations in cancer susceptibility genes …

Breast Cancer Research and Treatment

Pongtawat Lertwilaiwittaya

Ekkapong Roothumnong

Panee Nakthong

Peerawat Dungort

Chutima Meesamarnpong

...

2021/7

High Prevalence of Germline Mutations in Cancer Susceptibility Genes in Thai Patients with Clinical Spectrum of Hereditary Breast-Ovarian Cancer Syndrome

Pongtawat Lertwilaiwittaya

Ekkapong Roothumnong

Panee Nakthong

Peerawat Dungort

Chutima Meesamarnpong

...

2020/12/10

See List of Professors in Wanna Thongnoppakhun University(Mahidol University)