Madhulika Kabra - Concepedia

Author

Madhulika Kabra

All India Institute of Medical Sciences ORCID

Also Known As

E Gil-NTciga, Kabra, Madhulika, M Kabra, M. KABRA, M. Kabra, MADHULIKA KABRA, Madhulika Kabra, Madhusudan Kabra, Neerja Gupta, S K Kabra

485

Publications

7.7K

Citations

H-Index

270

Concepts

All Affiliations

All India Institute of Medical Sciences Sanjay Gandhi Post Graduate Institute of Medical Sciences Sir Ganga Ram Hospital Centre for DNA Fingerprinting and Diagnostics Kasturba Medical College, Manipal

About

Madhulika Kabra is an author at All India Institute of Medical Sciences specializing in medicine, pediatrics, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Education	8	8	247
2	Health Sciences	8	8	255
3	Arts	3	3	199
4	Engineering	1	1	37
5	Language Studies	1	1	18

Madhulika Kabra

194

Publications

Citations

H-Index

Page 1

	Year	Citations
Poly (propyleneimine) dendrimer based nanocontainers for targeting of efavirenz to human monocytes/macrophages<i>in vitro</i> Tathagata Dutta, Hrushikesh Agashe, Minakshi Garg, Journal of drug targeting	2007	155
Idiopathic chronic pancreatitis in India: phenotypic characterisation and strong genetic susceptibility due to <i>SPINK1</i> and <i>CFTR</i> gene mutations Shallu Midha, Rajni Khajuria, Shivaram Shastri, Gut	2010	122
Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39 Julie M. Schultz, Shaheen N. Khan, Zubair M. Ahmed, The American Journal of Human Genetics GeneticsAudiologyPathologyAuditory PhysiologyNonsyndromic Hearing Loss	2009	120
Prevalence of the triple X syndrome in phenotypically normal women with premature ovarian failure and its association with autoimmune thyroid disorders Ravinder Goswami, Deepti Goswami, Madhulika Kabra, Fertility and Sterility Normal WomenPremature Ovarian FailureThyroid DiseaseGynecologyThyroid Disorders	2003	119
Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness Saima Riazuddin, Shaheen N. Khan, Zubair M. Ahmed, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsPutative Cytoskeletal-organizing Protein	2005	110
Hydroxyurea in thalassemia intermedia—a promising therapy Ashish Dixit, T. Chatterjee, Pravas Mishra, Annals of Hematology MedicineHematologyPharmacotherapyHeme HomeostasisPharmacology	2005	108
Diagnosis and Management of Down Syndrome Neerja Gupta, Madhulika Kabra The Indian Journal of Pediatrics Down SyndromeNeurological DisorderDifferential DiagnosisPediatricsDiagnosis	2013	102
Incidence of acute kidney injury in hospitalized children Poonam Mehta, Aditi Sinha, Abdus Sami, Indian Pediatrics HemodialysisPediatric EpidemiologyMedicineKidney FailurePediatrics	2011	95
Further characterization of ATP6V0A2-related autosomal recessive cutis laxa Björn Fischer‐Zirnsak, Aikaterini Dimopoulou, Johannes Egerer, Human Genetics GeneticsMolecular GeneticsMolecular ResearchMedicineFurther Characterization	2012	93
Mutational spectrum of<i>MYO15A</i>: the large N-terminal extension of myosin XVA is required for hearing N. Nal, Zubair M. Ahmed, Engin Erkal, Human Mutation	2007	91

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