Vimla S. Aggarwal - Concepedia

Author

Vimla S. Aggarwal

Columbia University Irving Medical Center ORCID

Also Known As

Aggarwal V, Dr. Vandana Aggarwal, Joshua L. Deignan, Sandeep N. Wontakal, V Aggarwal, V. Aggarwal, Vimla Aggarwal, Vimla S Aggarwal, Vimla S. Aggarwal

191

Publications

5.2K

Citations

H-Index

Concepts

All Affiliations

Columbia University Irving Medical Center Columbia University Albert Einstein College of Medicine University of North Carolina at Chapel Hill Boston Children's Hospital

About

Vimla S. Aggarwal is an author at Columbia University Irving Medical Center specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	22	1.5K
2	Health Sciences	3	3	183
3	Natural Sciences	2	2	69
4	Education	1	1	50
5	Public Health	1	1	590

Vimla S. Aggarwal

Publications

4.5K

Citations

H-Index

Page 1

	Year	Citations
Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis Ronald J. Wapner, Brynn Levy, Blake C. Ballif, New England Journal of Medicine	2012	1.4K
Diagnostic Utility of Exome Sequencing for Kidney Disease Emily Groopman, Maddalena Marasà, Sophia Cameron‐Christie, New England Journal of Medicine	2018	722
Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study Slavé Petrovski, Vimla S. Aggarwal, Jessica L. Giordano, The Lancet Developmental AnomalySequencingWhole-exome SequencingGeneticsGenetic Epidemiology	2019	590
Genomic Imbalance in Products of Conception Brynn Levy, Styrmir Sigurjonsson, B. Pettersen, Obstetrics and Gynecology	2014	244
Identification of downstream genetic pathways of Tbx1 in the second heart field Jun Liao, Vimla S. Aggarwal, Sonja Nowotschin, Developmental Biology Downstream Genetic PathwaysSecond Heart FieldSystems BiologyCardiomyopathyCardiac Muscle	2008	143
Chromosomal Microarray Versus Karyotyping for Prenatal Diagnosis Ronald J. Wapner, Christa Lese Martin, Brynn Levy, Obstetrical & Gynecological Survey	2013	134
Causal Genetic Variants in Stillbirth Kate E. Stanley, Jessica L. Giordano, Vanessa Thorsten, New England Journal of Medicine	2020	130
Dual embryonic origin of the mammalian otic vesicle forming the inner ear Laina Freyer, Vimla S. Aggarwal, Bernice E. Morrow Development Organ DevelopmentAnatomyEmbryologyInner Ear MorphogenesisTissue Development	2011	118
Glut1 deficiency syndrome and erythrocyte glucose uptake assay Hong Yang, Dong Wang, Kristin Engelstad, Annals of Neurology	2011	107
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome Margot A. Cousin, Blake A. Creighton, Keith A. Breau, Nature Genetics Developmental AnomalyPathogenic Sptbn1 VariantsBrain DevelopmentMedicineGenetics	2021	98

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