Nitin Sabherwal

566 total citations
14 papers, 401 citations indexed

About

Nitin Sabherwal is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Nitin Sabherwal has authored 14 papers receiving a total of 401 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Cell Biology and 4 papers in Genetics. Recurrent topics in Nitin Sabherwal's work include Microtubule and mitosis dynamics (4 papers), Genomics and Chromatin Dynamics (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Nitin Sabherwal is often cited by papers focused on Microtubule and mitosis dynamics (4 papers), Genomics and Chromatin Dynamics (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Nitin Sabherwal collaborates with scholars based in United Kingdom, Germany and United States. Nitin Sabherwal's co-authors include Nancy Papalopulu, Gudrun Rappold, Katja Schneider, Berenika Płusa, Joanna B. Grabarek, Néstor Saiz, Rüdiger J. Blaschke, Antonio Marchini, Johannes Kapeller and Cheryll Tickle and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Development and Journal of Cell Science.

In The Last Decade

Nitin Sabherwal

14 papers receiving 399 citations

Peers

Countries citing papers authored by Nitin Sabherwal

Since Specialization

Citations

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

Fields of papers citing papers by Nitin Sabherwal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nitin Sabherwal

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Inhibiting ERK5 Overcomes Breast Cancer Resistance to Anti-HER2 Therapy By Targeting the G1–S Cell-Cycle Transition 2022 ·Cancer Research Communications ·Jingwei Zhang, Adam J. Pearson, Nitin Sabherwal, Brian A. Telfer, (unknown), (unknown), Qiuping Xu, Wei Zhang, Fuhui Chen, Shiyang Li, Jinhua Wang, Nathanael S. Gray, (unknown), Katherine G. Finegan, Michael Cross, Emanuele Giurisato, Alan J. Whitmarsh, Cathy Tournier	5
2	Bilateral Feedback in Oscillator Model Is Required to Explain the Coupling Dynamics of Hes1 with the Cell Cycle 2022 ·Mathematics ·(unknown), Nitin Sabherwal, Nancy Papalopulu	1
3	Differential phase register of Hes1 oscillations with mitoses underlies cell-cycle heterogeneity in ER ⁺ breast cancer cells 2021 ·Proceedings of the National Academy of Sciences ·Nitin Sabherwal, (unknown), Elli Marinopoulou, (unknown), (unknown), (unknown), Ximena Soto, Jochen Kursawe, Nancy Papalopulu	12
4	HES1 protein oscillations are necessary for neural stem cells to exit from quiescence 2021 ·iScience ·Elli Marinopoulou, Veronica Biga, Nitin Sabherwal, (unknown), (unknown), Antony Adamson, Nancy Papalopulu	20
5	aPKC Phosphorylates p27Xic1, Providing a Mechanistic Link between Apicobasal Polarity and Cell-Cycle Control 2014 ·Developmental Cell ·Nitin Sabherwal, Raphaël Thuret, Robert Lea, Peter Stanley, Nancy Papalopulu	16
6	Atypical protein kinase C couples cell sorting with primitive endoderm maturation in the mouse blastocyst 2013 ·Development ·Néstor Saiz, Joanna B. Grabarek, Nitin Sabherwal, Nancy Papalopulu, Berenika Płusa	57
7	Apicobasal polarity and cell proliferation during development 2012 ·Essays in Biochemistry ·Nitin Sabherwal, Nancy Papalopulu	8
8	pTransgenesis: a cross-species, modular transgenesis resource 2011 ·Development ·Nick R. Love, Raphaël Thuret, Yaoyao Chen, Shoko Ishibashi, Nitin Sabherwal, Roberto Paredes, (unknown), Karel Dorey, Anna Noble, Matthew Guille, Yoshiki Sasai, Nancy Papalopulu, Enrique Amaya	46
9	The apicobasal polarity kinase aPKC functions as a nuclear determinant and regulates cell proliferation and fate duringXenopusprimary neurogenesis 2009 ·Development ·Nitin Sabherwal, (unknown), Sarah Hodge, Jun Wei, Andrew D. Chalmers, Nancy Papalopulu	35
10	Long-range conserved non-coding SHOX sequences regulate expression in developing chicken limb and are associated with short stature phenotypes in human patients 2006 ·Human Molecular Genetics ·Nitin Sabherwal, Fiona Bangs, Rainer Roth, (unknown), (unknown), Eva Tiecke, Georg Klaus Hinkel, (unknown), B. P. Hauffa, H van Kamp, Johannes Kapeller, Cheryll Tickle, Gudrun Rappold	90
11	Alteration of DNA binding, dimerization, and nuclear translocation of SHOX homeodomain mutations identified in idiopathic short stature and Leri-Weill dyschondrosteosis 2005 ·Human Mutation ·Katja Schneider, Antonio Marchini, Nitin Sabherwal, Ralph Röth, Beate Niesler, (unknown), Rüdiger J. Blaschke, Margaret L. Lawson, Miroslav Dumić, Gudrun Rappold	36
12	Identification of a Major Recombination Hotspot in Patients with Short Stature and SHOX Deficiency 2005 ·The American Journal of Human Genetics ·Katja Schneider, Nitin Sabherwal, (unknown), Ralph Röth, (unknown), Werner Blum, Gordon B. Cutler, Gudrun Rappold	31
13	A novel point mutation A170P in the SHOX gene defines impaired nuclear translocation as a molecular cause for Léri–Weill dyschondrosteosis and Langer dysplasia 2004 ·Journal of Medical Genetics ·Nitin Sabherwal, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	19
14	Impairment of SHOX nuclear localization as a cause for Leri-Weill syndrome 2004 ·Journal of Cell Science ·Nitin Sabherwal, Katja Schneider, Rüdiger J. Blaschke, Antonio Marchini, Gudrun Rappold	25

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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