Concepedia

Author

Prateek Gupta

The University of Texas Health Science Center at HoustonORCID

Also Known As

P A Gupta, P Gupta, Prateek A. Gupta, Prateek Anand Gupta, Prateek Gupta

19

Publications

548

Citations

9

H-Index

12

Concepts

All Affiliations

The University of Texas Health Science Center at HoustonUniversitas Gadjah MadaThe University of Texas at Austin
PG

About

Prateek Gupta is an author at The University of Texas Health Science Center at Houston specializing in medicine, pathology, and molecular genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

3

3

157

2

Molecular Genetics

2

2

43

3

Pathology

2

2

43

4

Diabetes

1

1

114

5

Epidemiology

1

1

114

Prateek Gupta

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7

Publications

417

Citations

7

H-Index

YearCitations

Ten novel<i>FBN2</i>mutations in congenital contractural arachnodactyly: Delineation of the molecular pathogenesis and clinical phenotype

Prateek Gupta, Elizabeth A. Putnam, Sonya G. Carmical,

Human Mutation

2001

140

Prevalence of Diabetic Retinopathy and Blindness in Indonesian Adults With Type 2 Diabetes

Muhammad Bayu Sasongko, Felicia Widyaputri, Angela Nurini Agni,

American Journal of Ophthalmology

2017

114

The<i>FBN2</i>gene: new mutations, locus-specific database (Universal Mutation Database<i>FBN2</i>), and genotype-phenotype correlations

Melissa Yana Frédéric, Christine Monino, Christoph Marschall,

Human Mutation

2008

63

Associations of Physical Activity and Sedentary Behaviour with Vision-Threatening Diabetic Retinopathy in Indonesian Population with Type 2 Diabetes Mellitus: Jogjakarta Eye Diabetic Study in the Community (JOGED.COM)

D.P Dharmastuti, Angela Nurini Agni, Felicia Widyaputri,

Ophthalmic Epidemiology

2017

29

Characterization of an Aquaporin-2 Water Channel Gene Mutation Causing Partial Nephrogenic Diabetes Insipidus in a Mexican Family

Cristina Boccalandro, Fabrizio De Mattia, Dong-Chuan Guo,

Journal of the American Society of Nephrology

2004

28

Paucity of skeletal manifestations in hispanic families with FBN1 mutations

Carlos Villamizar, Ellen S. Regalado, Van Tran Fadulu,

European Journal of Medical Genetics

2009

22

An FBN1 pseudoexon mutation in a patient with Marfan syndrome: confirmation of cryptic mutations leading to disease

Dongchuan Guo, Prateek Gupta, Van Tran‐Fadulu,

Journal of Human Genetics

2008

21

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