Concepedia

Author

Massupa Kaewgahya

Chiang Mai University

Also Known As

Jorge Paolinelli, M. Kaewgahya, Massupa Kaewgahya

21

Publications

369

Citations

12

H-Index

19

Concepts

All Affiliations

Chiang Mai UniversityMaharaj Nakorn Chiang Mai HospitalSuranaree University of TechnologyNiigata UniversityChulabhorn Research Institute
MK

About

Massupa Kaewgahya is an author at Chiang Mai University specializing in medicine, pathology, and genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

5

5

127

2

Pathology

5

5

126

3

Public Health

1

1

13

4

Craniofacial Development

1

1

50

5

Developmental Biology

1

1

50

Massupa Kaewgahya

×

12

Publications

336

Citations

12

H-Index

YearCitations

Enamel‐renal‐gingival syndrome and <i>FAM20A</i> mutations

Piranit Nik Kantaputra, Massupa Kaewgahya, Udomrat Khemaleelakul,

American Journal of Medical Genetics Part A

2013

56

<i>GREMLIN 2</i> Mutations and Dental Anomalies

Piranit Nik Kantaputra, Massupa Kaewgahya, Athiwat Hatsadaloi,

Journal of Dental Research

2015

50

<i>WNT10B</i> mutations associated with isolated dental anomalies

Piranit Nik Kantaputra, Athiwat Hutsadaloi, Massupa Kaewgahya,

Clinical Genetics

2018

40

Tricho‐odonto‐onycho‐dermal dysplasia and <i>WNT10A</i> mutations

Piranit Nik Kantaputra, Massupa Kaewgahya, Dhirawat Jotikasthira,

American Journal of Medical Genetics Part A

2014

39

<i>WNT</i><i>10</i><i>A</i> mutations also associated with agenesis of the maxillary permanent canines, a separate entity

Piranit Nik Kantaputra, Massupa Kaewgahya, Warissara Kantaputra

American Journal of Medical Genetics Part A

2013

30

Enamel–Renal–Gingival syndrome, hypodontia, and a novel <i>FAM20A</i> mutation

Piranit Nik Kantaputra, Chotika Bongkochwilawan, Massupa Kaewgahya,

American Journal of Medical Genetics Part A

2014

25

Periodontal disease and FAM20A mutations

Piranit Nik Kantaputra, Chotika Bongkochwilawan, Mark Lubinsky,

Journal of Human Genetics

2017

25

Mutations in <scp> <i>LRP5</i> </scp> and <scp> <i>BMP4</i> </scp> are associated with mesiodens, tooth agenesis, root malformation, and oral exostoses

Piranit Nik Kantaputra, Yeliz Güven, Kanich Tripuwabhrut,

Clinical Genetics

2022

19

TFAP2B mutation and dental anomalies

Natchaya Tanasubsinn, Rekwan Sittiwangkul, Yupada Pongprot,

Journal of Human Genetics

2017

14

Cutis laxa with pulmonary emphysema, conjunctivochalasis, nasolacrimal duct obstruction, abnormal hair, and a novel <i>FBLN5</i> mutation

Piranit Nik Kantaputra, Massupa Kaewgahya, Atchareeya Wiwatwongwana,

American Journal of Medical Genetics Part A

2014

13

Page 1