Hannah M. Mitchison

14.7k total citations
114 papers, 5.0k citations indexed

About

Hannah M. Mitchison is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Hannah M. Mitchison has authored 114 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 46 papers in Physiology and 43 papers in Genetics. Recurrent topics in Hannah M. Mitchison's work include Lysosomal Storage Disorders Research (44 papers), Genetic and Kidney Cyst Diseases (34 papers) and Cystic Fibrosis Research Advances (29 papers). Hannah M. Mitchison is often cited by papers focused on Lysosomal Storage Disorders Research (44 papers), Genetic and Kidney Cyst Diseases (34 papers) and Cystic Fibrosis Research Advances (29 papers). Hannah M. Mitchison collaborates with scholars based in United Kingdom, United States and Netherlands. Hannah M. Mitchison's co-authors include Enza Maria Valente, Jonathan D. Cooper, Sara Mole, Eddie M.K. Chung, Claire Hogg, Patricia B. Munroe, Amelia Shoemark, Maggie Meeks, Mitali Patel and R. Mark Gardiner and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Hannah M. Mitchison

109 papers receiving 4.9k citations

Peers

Countries citing papers authored by Hannah M. Mitchison

Since Specialization

Citations

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

Fields of papers citing papers by Hannah M. Mitchison

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hannah M. Mitchison. 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 Hannah M. Mitchison. The network helps show where Hannah M. Mitchison may publish in the future.

Co-authorship network of co-authors of Hannah M. Mitchison

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Characterisation of a primary ciliary dyskinesia model generated from BMI1 -transduced basal epithelial cells 2025 ·Journal of Cell Science ·(unknown), Eriomina Shahaj, (unknown), Dani Do Hyang Lee, Anna Straatman-Iwanowska, Hannah M. Mitchison, Deborah L. Baines, Robert A. Hirst, Claire Hogg, Christopher O’Callaghan, Stephen L. Hart	0
2	Axonemal structures reveal mechanoregulatory and disease mechanisms 2023 ·Nature ·Travis Walton, Miao Gui, (unknown), Mahmoud R. Fassad, Robert A. Hirst, Eric G. Haarman, Christopher O’Callaghan, Mathieu Bottier, Thomas Burgoyne, Hannah M. Mitchison, Alan Brown	75
3	PCD Detect: enhancing ciliary features through image averaging and classification 2020 ·American Journal of Physiology-Lung Cellular and Molecular Physiology ·Amelia Shoemark, Andreia Pinto, Mitali Patel, (unknown), Claire Hogg, Hannah M. Mitchison, Thomas Burgoyne	10
4	Clinical and genetic spectrum in 33 Egyptian families with suspected primary ciliary dyskinesia 2019 ·Clinical Genetics ·Mahmoud R. Fassad, (unknown), Heba Morsy, Mitali Patel, Nesrine Radwan, Lucy Jenkins, Thomas Cullup, Eman Mahmoud Fouda, Hannah M. Mitchison, (unknown)	15
5	Mechanical loading inhibits cartilage inflammatory signalling via an HDAC6 and IFT-dependent mechanism regulating primary cilia elongation 2019 ·Osteoarthritis and Cartilage ·Shaoyin Fu, (unknown), (unknown), W. Wang, J. Paul Chapple, Hannah M. Mitchison, Philip L. Beales, A.K. Wann, Martin M. Knight	61
6	Primary Ciliary Dyskinesia Due to Microtubular Defects is Associated with Worse Lung Clearance Index 2018 ·Lung ·Samantha Irving, Matthew A. Dixon, Mahmoud R. Fassad, Emily Frost, Jane Hayward, (unknown), Sarah Ollosson, Alexandros Onoufriadis, Mitali Patel, Juliet Scully, S.B. Carr, Hannah M. Mitchison, Michael R. Loebinger, Claire Hogg, Amelia Shoemark, Andrew Bush	19
7	Accuracy of Immunofluorescence in the Diagnosis of Primary Ciliary Dyskinesia 2017 ·American Journal of Respiratory and Critical Care Medicine ·Amelia Shoemark, Emily Frost, Mellisa Dixon, Sarah Ollosson, (unknown), Mitali Patel, Juliet Scully, Andrew Rogers, Hannah M. Mitchison, Andrew Bush, Claire Hogg	77
8	Diagnosis and management of primary ciliary dyskinesia 2014 ·Archives of Disease in Childhood ·Jane S. Lucas, A. E. Burgess, Hannah M. Mitchison, Eduardo Moya, (unknown), Claire Hogg, (unknown)	166
9	PTU-112 Rifaximin for Hepatic Encephalopathy is Cost Effective at Reducing Emergency Hospital Admission 2013 ·Gut ·James Orr, (unknown), Hannah M. Mitchison, (unknown), Sushma Saksena, Jeff S. Topping, (unknown), (unknown), (unknown), Mark Hudson	2
10	Bioinformatic perspectives in the neuronal ceroid lipofuscinoses 2012 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Stanislav Kmoch, Viktor Stránecký, Richard D. Emes, Hannah M. Mitchison	6
11	Transcript and in silico analysis of CLN3 in juvenile neuronal ceroid lipofuscinosis and associated mouse models 2008 ·Human Molecular Genetics ·Chun Hung Chan, Hannah M. Mitchison, David A. Pearce	30
12	Progress towards understanding disease mechanisms in small vertebrate models of neuronal ceroid lipofuscinosis 2006 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Jonathan D. Cooper, Claire Russell, Hannah M. Mitchison	80
13	Batten disease (JNCL) is linked to disturbances in mitochondrial, cytoskeletal, and synaptic compartments 2006 ·Journal of Neuroscience Research ·Kaisu Luiro, Outi Kopra, Tomas Blom, Massimiliano Gentile, Hannah M. Mitchison, Iiris Hovatta, Kid Törnquist, Anu Jalanko	63
14	DNAH3: Characterization of the sequence and mutation search in patients with Primary Ciliary Dyskinesia 2002 ·European Journal of Human Genetics ·(unknown), Corinne Gehrig, M Armengot, M Rutishauser, Mark Jorissen, (unknown), Lucia Bartoloni, Colette Rossier, (unknown), Nathalie Scamuffa, Hannah M. Mitchison, (unknown), Stylianos E. Antonarakis	5
15	Continued retinal function despite NCL pathology in a Cln3 knockout mouse model of Juvenile Neuronal Ceroid Lipofuscinosis (Batten Disease) 2002 ·Investigative Ophthalmology & Visual Science ·(unknown), Andrew Lotery, (unknown), Mark Turmaine, Beverly L. Davidson, (unknown), Hannah M. Mitchison	1
16	Targeted disruption of the Cln3 gene provides a mouse model for Batten disease (vol 6, pg 321, 1999) 2000 ·UCL Discovery (University College London) ·Hannah M. Mitchison, (unknown), (unknown), Jonathan D. Cooper, (unknown), (unknown), Nathalie De Vos, M.H. Breuning, (unknown), WC Mobley, (unknown), (unknown), (unknown), (unknown)	0
17	A murine model for juvenile NCL: Gene targeting of mouse CLn3 (vol 66, pg 309, 1999) 1999 ·UCL Discovery (University College London) ·(unknown), (unknown), (unknown), (unknown), Nathalie De Vos, M.H. Breuning, (unknown), Sara Mole, (unknown), Hannah M. Mitchison	0
18	Molecular basis of the neuronal ceroid lipofuscinoses: Mutations inCLN1,CLN2,CLN3, andCLN5 1999 ·Human Mutation ·Sara Mole, Hannah M. Mitchison, Patricia B. Munroe	47
19	Refined localization of the Batten disease gene (CLN3) by haplotype and linkage disequilibrium mapping to D16S288-16S383 and exclusion from this region of a variant form of Batten disease with granular osmiophilic deposits 1995 ·The American Journal of Human Genetics ·Hannah M. Mitchison	1
20	Genetic heterogeneity in juvenile NCL 1994 ·The American Journal of Human Genetics ·Y Hart, E. Andermann, Hannah M. Mitchison	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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