Rani Sachdev

2.3k total citations
26 papers, 237 citations indexed

About

Rani Sachdev is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Rani Sachdev has authored 26 papers receiving a total of 237 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 10 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Rani Sachdev's work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Childhood Cancer Survivors' Quality of Life (4 papers). Rani Sachdev is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Childhood Cancer Survivors' Quality of Life (4 papers). Rani Sachdev collaborates with scholars based in Australia, United States and United Kingdom. Rani Sachdev's co-authors include John Christodoulou, Marcia L. Budarf, Meredith Wilson, Alison Colley, Leon R. McQuade, Elizabeth E. Palmer, B S Emanuel, Rebecca Macintosh, Michael Cardamone and John A. Lawson and has published in prestigious journals such as SHILAP Revista de lepidopterología, Cell Reports and Neuropharmacology.

In The Last Decade

Rani Sachdev

26 papers receiving 235 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Rani Sachdev Australia 7 137 110 37 30 27 26 237
Andrea Guerin Canada 8 99 0.7× 103 0.9× 19 0.5× 69 2.3× 12 0.4× 30 336
Cheuk Wing Fung China 9 67 0.5× 54 0.5× 31 0.8× 42 1.4× 15 0.6× 18 177
I. Desguerre France 12 194 1.4× 69 0.6× 98 2.6× 64 2.1× 18 0.7× 37 400
Xena Giada Pappalardo Italy 8 170 1.2× 58 0.5× 24 0.6× 28 0.9× 5 0.2× 32 263
Kelly L. Jones United States 8 81 0.6× 90 0.8× 7 0.2× 23 0.8× 15 0.6× 14 194
Lacey Smith United States 10 130 0.9× 207 1.9× 139 3.8× 65 2.2× 12 0.4× 20 393
Esperanza Font–Montgomery United States 9 183 1.3× 193 1.8× 17 0.5× 59 2.0× 13 0.5× 14 334
Elke Hobbiebrunken Germany 8 133 1.0× 76 0.7× 7 0.2× 34 1.1× 7 0.3× 11 268
Naomi Meeks United States 8 86 0.6× 50 0.5× 15 0.4× 36 1.2× 18 0.7× 16 169
Paula Frassinetti Vasconcelos de Medeiros Brazil 10 110 0.8× 78 0.7× 17 0.5× 22 0.7× 5 0.2× 24 241

Countries citing papers authored by Rani Sachdev

Since Specialization
Citations

This map shows the geographic impact of Rani Sachdev'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 Rani Sachdev with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rani Sachdev more than expected).

Fields of papers citing papers by Rani Sachdev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rani Sachdev. 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 Rani Sachdev. The network helps show where Rani Sachdev may publish in the future.

Co-authorship network of co-authors of Rani Sachdev

This figure shows the co-authorship network connecting the top 25 collaborators of Rani Sachdev. A scholar is included among the top collaborators of Rani Sachdev 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 Rani Sachdev. Rani Sachdev is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Harms, Frederike L., Jessica E. Rexach, Stéphanie Efthymiou, et al.. (2024). Loss of TBC1D2B causes a progressive neurological disorder with gingival overgrowth. European Journal of Human Genetics. 32(5). 558–566. 1 indexed citations
2.
3.
Robertson, Eden G., N Roberts, Rebecca Macintosh, et al.. (2023). “Somewhere to turn to with my questions”: A pre-post pilot of an information linker service for caregivers who have a child with a Developmental and Epileptic Encephalopathy. European Journal of Paediatric Neurology. 47. 94–104. 5 indexed citations
4.
McKee, Shane, Paolo Prontera, Francesca Faravelli, et al.. (2022). SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome. Genes. 13(2). 252–252. 1 indexed citations
5.
Wang, Meng, Åsa Andersson, Elizabeth E. Palmer, et al.. (2022). Anti-seizure mechanisms of midazolam and valproate at the β2(L51M) variant of the GABAA receptor. Neuropharmacology. 221. 109295–109295. 1 indexed citations
6.
Nevin, Suzanne M., Claire E. Wakefield, Rebecca Macintosh, et al.. (2022). Piloting positive psychology resources for caregivers of a child with a genetic developmental and epileptic encephalopathy. European Journal of Paediatric Neurology. 37. 129–138. 5 indexed citations
7.
Baynam, Gareth, Lisa Ewans, Lynn Greenhalgh, et al.. (2022). Distinctive Brain Malformations in Zhu-Tokita-Takenouchi-Kim Syndrome. American Journal of Neuroradiology. 43(11). 1660–1666. 1 indexed citations
8.
Robertson, Eden G., Lauren Kelada, Stephanie Best, et al.. (2022). Acceptability and feasibility of an online information linker service for caregivers who have a child with genetic epilepsy: a mixed-method pilot study protocol. BMJ Open. 12(10). e063249–e063249. 6 indexed citations
9.
Nevin, Suzanne M., et al.. (2022). Hope in the uncertainties and certainty for parents of children with rare neurological disorders: Part 2 (of 3): Certainty. Journal of Paediatrics and Child Health. 58(10). 1722–1725. 4 indexed citations
10.
Macintosh, Rebecca, et al.. (2022). Hope in the uncertainties and certainty for parents of children with rare neurological disorders: Part 3 (of 3): Hope. Journal of Paediatrics and Child Health. 58(10). 1726–1728. 2 indexed citations
11.
Palmer, Elizabeth E., et al.. (2022). Hope in the uncertainties and certainty for parents of children with rare neurological disorders. Part I (of 3): Uncertainty. Journal of Paediatrics and Child Health. 58(10). 1718–1721. 9 indexed citations
12.
Nevin, Suzanne M., Claire E. Wakefield, Ann Dadich, et al.. (2021). Hearing parents' voices: A priority-setting workshop to inform a suite of psychological resources for parents of children with rare genetic epilepsies. SHILAP Revista de lepidopterología. 1. 100014–100014. 6 indexed citations
13.
14.
Harms, Frederike L., Malik Alawi, Sigrid Fuchs, et al.. (2020). Biallelic loss‐of‐function variants in TBC1D2B cause a neurodevelopmental disorder with seizures and gingival overgrowth. Human Mutation. 41(9). 1645–1661. 13 indexed citations
15.
Palmer, Elizabeth E., Tejaswi Kandula, Rebecca Macintosh, et al.. (2017). A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic Encephalopathy. Cell Reports. 21(4). 926–933. 33 indexed citations
16.
Palmer, Elizabeth E., Rani Sachdev, Michael Cardamone, et al.. (2015). Asparagine Synthetase Deficiency causes reduced proliferation of cells under conditions of limited asparagine. Molecular Genetics and Metabolism. 116(3). 178–186. 39 indexed citations
17.
Andrews, Ian, et al.. (2013). Ataxia Telangiectasia in a Three-Year-Old-Girl. Pediatric Neurology. 50(3). 279–280. 1 indexed citations
18.
Kamien, Benjamin, Michael Cardamone, John A. Lawson, & Rani Sachdev. (2012). A genetic diagnostic approach to infantile epileptic encephalopathies. Journal of Clinical Neuroscience. 19(7). 934–941. 19 indexed citations
19.
Monagle, Paul, David Mowat, Susan Russell, et al.. (2011). Australian Paediatric Surveillance Unit study of haemoglobinopathies in Australian children. Journal of Paediatrics and Child Health. 48(4). 356–360. 4 indexed citations
20.
Gabbett, Michael T., Stephen P. Robertson, Roland Broadbent, et al.. (2008). Characterizing the oculoauriculofrontonasal syndrome. Clinical Dysmorphology. 17(2). 79–85. 16 indexed citations

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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