Malavika Hebbar

624 total citations
19 papers, 290 citations indexed

About

Malavika Hebbar is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Malavika Hebbar has authored 19 papers receiving a total of 290 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Clinical Biochemistry. Recurrent topics in Malavika Hebbar's work include Genomics and Rare Diseases (5 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (4 papers). Malavika Hebbar is often cited by papers focused on Genomics and Rare Diseases (5 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (4 papers). Malavika Hebbar collaborates with scholars based in India, United States and Germany. Malavika Hebbar's co-authors include Katta M. Girisha, Anju Shukla, Stephanie Bielas, Rajagopal Kadavigere, Anshika Srivastava, Raoul Heller, Bart Loeys, Ólafur Þ. Magnússon, Brunhilde Wirth and Markus Storbeck and has published in prestigious journals such as The American Journal of Human Genetics, European Journal of Human Genetics and Clinical Genetics.

In The Last Decade

Malavika Hebbar

18 papers receiving 290 citations

Peers

Countries citing papers authored by Malavika Hebbar

Since Specialization

Citations

This map shows the geographic impact of Malavika Hebbar's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Malavika Hebbar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Malavika Hebbar more than expected).

Fields of papers citing papers by Malavika Hebbar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Malavika Hebbar. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Malavika Hebbar. The network helps show where Malavika Hebbar may publish in the future.

Co-authorship network of co-authors of Malavika Hebbar

This figure shows the co-authorship network connecting the top 25 collaborators of Malavika Hebbar. A scholar is included among the top collaborators of Malavika Hebbar based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Malavika Hebbar. Malavika Hebbar is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Biallelic Variant, c.644‐13_644‐9del in UNC50 Is Associated With Congenital Myasthenia Syndrome 2025 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), Malavika Hebbar, Shyamala Guruvare, (unknown), Gandham SriLakshmi Bhavani, (unknown), Katta M. Girisha, Anju Shukla, Shalini S. Nayak	0
2	Expanding the genotype-phenotype spectrum in SCN8A-related disorders 2024 ·BMC Neurology ·Malavika Hebbar, (unknown), (unknown), Cyrus Boelman, Richard A. Dean, Samuel J. Goodchild, Janette Mezeyova, Noah Gregory Shuart, J. P. Johnson, James Lee, Aspasia Michoulas, Linda Huh, Linlea Armstrong, Mary Connolly, Michelle Demos	2
3	Biallelic start loss variant, c. 1A > G in GCSH is associated with variant nonketotic hyperglycinemia 2021 ·Clinical Genetics ·(unknown), (unknown), Malavika Hebbar, Rajagopal Kadavigere, (unknown), Katta M. Girisha, Anju Shukla	3
4	A neurodegenerative mitochondrial disease phenotype due to biallelic loss‐of‐function variants in PNPLA8 encoding calcium‐independent phospholipase A2γ 2018 ·American Journal of Medical Genetics Part A ·(unknown), Russell P. Saneto, Malavika Hebbar, Ghayda Mirzaa, Katta M. Girisha	18
5	Bi-allelic c.181_183delTGT in BTB domain of KLHL7 is associated with overlapping phenotypes of Crisponi/CISS1-like and Bohring-Opitz like syndrome 2018 ·European Journal of Medical Genetics ·(unknown), Malavika Hebbar, Stephanie Bielas, Katta M. Girisha, Anju Shukla	8
6	Clinical and genetic spectrum of AMPD2-related pontocerebellar hypoplasia type 9 2018 ·European Journal of Human Genetics ·Fanny Kortüm, Rami Abou Jamra, Malik Alawi, Susan A. Berry, Guntram Borck, Katherine L. Helbig, Sha Tang, Dagmar Huhle, Georg Christoph Korenke, Malavika Hebbar, Anju Shukla, Katta M. Girisha, Maja Steinlin, (unknown), Martino Montomoli, Renzo Guerrini, Johannes R. Lemke, Kerstin Kutsche	23
7	A biallelic 36-bp insertion in PIBF1 is associated with Joubert syndrome 2018 ·Journal of Human Genetics ·Malavika Hebbar, (unknown), Anju Shukla, Stephanie Bielas, Katta M. Girisha	11
8	Genetic diversity of NDUFV1-dependent mitochondrial complex I deficiency 2018 ·European Journal of Human Genetics ·Anshika Srivastava, Kinshuk Raj Srivastava, Malavika Hebbar, (unknown), (unknown), Fengyun Su, Xuhong Cao, Arul M. Chinnaiyan, Katta M. Girisha, Anju Shukla, Stephanie Bielas	12
9	Locus and allelic heterogeneity in five families with hereditary spastic paraplegia 2018 ·Journal of Human Genetics ·Malavika Hebbar, Anju Shukla, Sheela Nampoothiri, Stephanie Bielas, Katta M. Girisha	7
10	Report of four novel variants in ASNS causing asparagine synthetase deficiency and review of literature 2018 ·Congenital Anomalies ·(unknown), Malavika Hebbar, (unknown), (unknown), Rajagopal Kadavigere, Anshika Srivastava, Stephanie Bielas, Katta M. Girisha, Anju Shukla	16
11	p.Arg69Trp in RNASEH2C is a founder variant in three Indian families with Aicardi–Goutières syndrome 2017 ·American Journal of Medical Genetics Part A ·Malavika Hebbar, (unknown), (unknown), Snehal Patil, Mamta Muranjan, (unknown), Vishnu Bhat B, Katta M. Girisha, (unknown)	2
12	Homozygous p.(Glu87Lys) variant in ISCA1 is associated with a multiple mitochondrial dysfunctions syndrome 2017 ·Journal of Human Genetics ·Anju Shukla, Malavika Hebbar, Anshika Srivastava, Rajagopal Kadavigere, (unknown), (unknown), Oliver Brandau, Stephanie Bielas, Katta M. Girisha	47
13	Homozygosity for a nonsense variant in AIMP2 is associated with a progressive neurodevelopmental disorder with microcephaly, seizures, and spastic quadriparesis 2017 ·Journal of Human Genetics ·Anju Shukla, Aneek Das Bhowmik, Malavika Hebbar, Rajagopal Kadavigere, Katta M. Girisha, Neerja Gupta, Ashwin Dalal	24
14	Homozygous c.359del variant in MGME1 is associated with early onset cerebellar ataxia 2017 ·European Journal of Medical Genetics ·Malavika Hebbar, Katta M. Girisha, Anshika Srivastava, Stephanie Bielas, Anju Shukla	6
15	Hyperphosphatasia with Mental Retardation Syndrome Due to a Novel Mutation in PGAP3 2017 ·Journal of Pediatric Genetics ·Sheela Nampoothiri, Malavika Hebbar, (unknown), (unknown), Stephanie Bielas, Anju Shukla, Katta M. Girisha	6
16	Identification of a novel LRRK1 mutation in a family with osteosclerotic metaphyseal dysplasia 2016 ·Journal of Human Genetics ·Long Guo, Katta M. Girisha, Aritoshi Iida, Malavika Hebbar, (unknown), Hitesh Shah, Gen Nishimura, Naomichi Matsumoto, (unknown), Noriko Miyake, Shiro Ikegawa	27
17	Biallelic Loss of Proprioception-Related PIEZO2 Causes Muscular Atrophy with Perinatal Respiratory Distress, Arthrogryposis, and Scoliosis 2016 ·The American Journal of Human Genetics ·(unknown), Markus Storbeck, Raoul Heller, Irmgard Hölker, Malavika Hebbar, Anju Shukla, Ólafur Þ. Magnússon, Sebahattin Çırak, Katta M. Girisha, Mary O’Driscoll, Bart Loeys, Brunhilde Wirth	72
18	Phenotypic variability in patients with interstitial 6q21‐q22 microdeletion and Acro–Cardio–Facial syndrome 2016 ·American Journal of Medical Genetics Part A ·Anju Shukla, Malavika Hebbar, Frederike L. Harms, Rajagopal Kadavigere, Katta M. Girisha, Kerstin Kutsche	4
19	[Pancreatic tuberculosis in systemic lupus]. 1994 ·PubMed ·Malavika Hebbar, Didier Gosset, (unknown), B Devulder	2

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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