M. Andrew Nesbit

5.4k citations

87 papers · 2.9k indexed · h-index 27

Impact in

Nephrology top 0.5%
- Parathyroid Disorders and Treatments
Genetics top 2%
- Genetic Syndromes and Imprinting

Papers in

Nephrology 19
- Parathyroid Disorders and Treatments 18
Ophthalmology 11

Co-authors: Rajesh V. Thakker Fadil Hannan Brian Harding Tara Moore Treena Cranston Sarah Howles Nigel Rust Paul T. Christie
Journals: The Journal of Clinical Endocrinology & Metabolism (9 papers)Scientific Reports (5 papers)Genomics (4 papers)Journal of Bone and Mineral Research (3 papers)Journal of Clinical Investigation (3 papers)
Partner nations: United Kingdom United States Denmark

In The Last Decade

M. Andrew Nesbit

84 papers receiving 2.8k citations

Peers

Countries citing papers authored by M. Andrew Nesbit

Since Specialization

Citations

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

Fields of papers citing papers by M. Andrew Nesbit

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside M. Andrew Nesbit, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with M. Andrew Nesbit Line = papers co-authored together M. Andrew Nesbit links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	TGFBI R124H mutant allele silencing in granular corneal dystrophy type 2 using topical siRNA delivery Journal of Controlled Release ·Hyun-Chul Shin, Amanda Kowalczyk, Paulina Rachwalska, Carla Elliott, 章三山本, Zhuoyu He, Jan J. Enghild, Diego Cobice, Nicolas Schwind, 好岳小林, Stefano Ferrari, Benjamin Patterson, Bundesministerium für Wirtschaft und Technologie, John Marshall, M. Andrew Nesbit, Tara Moore	2025	1
2	Topical mutant allele-specific siRNA delivery for treatment of Meesmann epithelial corneal dystrophy and elucidation of disease biomarkers Journal of Controlled Release ·Hyun-Chul Shin, I. V. Demydenko, Zhuoyu He, Benjamin Patterson, Carsten Scavenius, Jan J. Enghild, John Marshall, Paulina Rachwalska, Michael Welsh, Carla Elliott, Bundesministerium für Wirtschaft und Technologie, Colin E. Willoughby, M. Andrew Nesbit, Tara Moore	2025	0
3	A novel algorithm for cardiovascular screening using conjunctival microcirculatory parameters and blood biomarkers Scientific Reports ·Yard. Doç. Dr. Abdullah Ecehan, إشراف د حنان بنت عبد الرحمن العريني, M. Andrew Nesbit, Mark W. Ruddock, Paul Brennan, 邹杰华, S. Yunus, Iturralde Codina A, Dewar Finlay, Emanuele Trucco, Mary Jo Kurth, Salma Abd El Atty Moawed, John Lamont, Peter Fitzgerald, Mark S. Spence, James McLaughlin, Tara Moore	2022	8
4	Successful Proof-of-Concept for Topical Delivery of Novel Peptide ALM201 with Potential Usefulness for Treating Neovascular Eye Disorders SHILAP Revista de lepidopterología ·P. Diament, M. Andrew Nesbit, Diego Cobice, C. Logan Mackay, 美季川端, Manisha Bungsy, Aaron Cranston, Tara Moore	2022	2
5	Assessment of the conjunctival microcirculation for patients presenting with acute myocardial infarction compared to healthy controls Scientific Reports ·Paul Brennan, S. Yunus, Iturralde Codina A, Yard. Doç. Dr. Abdullah Ecehan, إشراف د حنان بنت عبد الرحمن العريني, 邹杰华, Dewar Finlay, Kevin Blighe, James McLaughlin, M. Andrew Nesbit, Emanuele Trucco, Tara Moore, Mark S. Spence	2021	14
6	User experience analysis of AbC-19 Rapid Test via lateral flow immunoassays for self-administrated SARS-CoV-2 antibody testing Scientific Reports ·Iturralde Codina A, Raymond Bond, 章三山本, إشراف د حنان بنت عبد الرحمن العريني, Amanda Kowalczyk, Ruth Price, William Burns, M. Andrew Nesbit, James McLaughlin, Tara Moore	2021	15
7	Topical siRNA delivery to the cornea and anterior eye by hybrid silicon-lipid nanoparticles Journal of Controlled Release ·Paulina Rachwalska, Cristóbal Kuskinen, Carla Elliott, Mukhtar H. Ahmed, Keith Thomas, M. Andrew Nesbit, Michael Welsh, Tara Moore, I. V. Demydenko	2020	45
8	Capsid Engineering Overcomes Barriers Toward Adeno-Associated Virus Vector-Mediated Transduction of Endothelial Cells Human Gene Therapy ·Mohammed Ghareeb, Axel Rossi, I. V. Shorokhova, Nadja Meumann, E.M. Zaichenko, Kathleen A. Christie, M. Andrew Nesbit, Casey Moore, Ulrich Hacker, Michael Morgan, Dirk Hoffmann, James Zengel, Jan E. Carette, Axel Schambach, Anna Salvetti, Margarete Odenthal, Hildegard Büning	2019	22
9	Effective In Vivo Topical Delivery of siRNA and Gene Silencing in Intact Corneal Epithelium Using a Modified Cell-Penetrating Peptide Molecular Therapy — Nucleic Acids ·Davide Schiroli, María J. Gómara, Eleonora Maurizi, Sarah D. Atkinson, Pasha Malla, Kathleen A. Christie, Diego Cobice, Cian M. McCrudden, M. Andrew Nesbit, Isabel Haro, Tara Moore	2019	33
10	Gene editing in the context of an increasingly complex genome BMC Genomics ·Kevin Blighe, Larry DeDionisio, Kathleen A. Christie, Bo Chawes, Araujo Cuauro, Thomais Kakouli‐Duarte, Korganbayeva G.A., T. N. Tudron, Rachel S. Kelly, Leandro Castellano, Justin Stebbing, Jessica Lasky‐Su, M. Andrew Nesbit, Tara Moore	2018	7
11	A novel role for CRIM1 in the corneal response to UV and pterygium development Experimental Eye Research ·Eleonora Maurizi, Davide Schiroli, Sarah D. Atkinson, Pasha Malla, David Courtney, Barry O’Hagan, Victoria McGilligan, Heloysa Amaral da Silva, Jenny C. Taylor, Marshad Abdullah Almutairi, Arulalan Veluppillai, Dave Goldsmith, Pieter A. Gouws, Jonathan E. Moore, M. Andrew Nesbit, Tara Moore	2018	12
12	Post-LASIK exacerbation of granular corneal dystrophy type 2 in members of a chinese family Eye ·Korganbayeva G.A., Geena George, Larry DeDionisio, Bilian Ke, M. Andrew Nesbit, John Marshall, Tara Moore	2017	10
13	Mutations Affecting G-Protein Subunit α₁₁in Hypercalcemia and Hypocalcemia New England Journal of Medicine ·M. Andrew Nesbit, Fadil Hannan, Sarah Howles, Valerie Babinsky, Rosie Head, Treena Cranston, Nigel Rust, Maurine R. Hobbs, Hunter Heath, Rajesh V. Thakker	2013	240
14	A calcium-sensing receptor (CaSR) variant, Glu250Lys, present in familial hypocalciuric hypercalcaemia (FHH) and autosomal dominant hypocalcaemic hypercalciuria (ADHH) probands represents a functionally neutral polymorphism: lessons for CaSR mutational analysis Fadil Hannan, M. Andrew Nesbit, Treena Cranston, Rajesh V. Thakker	2012	3
15	SEDLIN Forms Homodimers: Characterisation of SEDLIN Mutations and Their Interactions with Transcription Factors MBP1, PITX1 and SF1 PLoS ONE ·Jeshmi Jeyabalan, M. Andrew Nesbit, Juris Galvanovskis, Richard Callaghan, Patrik Rorsman, Rajesh V. Thakker	2010	21
16	A homozygous inactivating calcium‐sensing receptor mutation, Pro339Thr, is associated with isolated primary hyperparathyroidism: correlation between location of mutations and severity of hypercalcaemia Clinical Endocrinology ·Fadil Hannan, M. Andrew Nesbit, Paul T. Christie, Willy Lissens, Bart Van der Schueren, Marie Bex, Roger Bouillon, Rajesh V. Thakker	2010	37
17	The calcilytic agent NPS2143 rectifies hypocalcaemia in a mouse model, Nuf, that is due to an activating calcium-sensing-receptor (CaSR) mutation: relevance to autosomal dominant hypocalcaemia with hypercalciuria Fadil Hannan, Gerard Walls, Enikö Kállay, M. Andrew Nesbit, Tertius Hough, Roger Cox, Jianxin Hu, Allen M. Spiegel, Rajesh V. Thakker	2008	1
18	An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism Journal of Clinical Investigation ·Michael R. Bowl, M. Andrew Nesbit, Brian Harding, Elaine R. Levy, Andrew Jefferson, Emanuela V. Volpi, Karine Rizzoti, Robin Lovell‐Badge, David Schlessinger, Michael P. Whyte, Rajesh V. Thakker	2005	63
19	X-Linked Hypophosphatemia Attributable to Pseudoexons of the PHEX Gene The Journal of Clinical Endocrinology & Metabolism ·Paul T. Christie, Brian Harding, M. Andrew Nesbit, Michael P. Whyte, Rajesh V. Thakker	2001	48
20	Interaction of Osteopontin with Osteoclast Integrins^a Annals of the New York Academy of Sciences ·Michael A. Horton, M. Andrew Nesbit, Miep Helfrich	1995	43

About M. Andrew Nesbit

M. Andrew Nesbit is a scholar working on Nephrology, Ophthalmology, Genetics, Molecular Biology and Radiology, Nuclear Medicine and Imaging, having authored 87 papers that have together received 2.9k indexed citations. Recurring topics across this work include Parathyroid Disorders and Treatments (18 papers), Congenital heart defects research (11 papers), Erythrocyte Function and Pathophysiology (10 papers), Corneal surgery and disorders (10 papers), Genetic Syndromes and Imprinting (8 papers), CRISPR and Genetic Engineering (8 papers), Corneal Surgery and Treatments (8 papers) and RNA Interference and Gene Delivery (7 papers). The work is most often cited by research in Nephrology (830 citations), Genetics (720 citations), Molecular Biology (1.6k citations), Sensory Systems (73 citations) and Aging (25 citations). M. Andrew Nesbit has collaborated with scholars based in United Kingdom, United States and Denmark. Frequent co-authors include Rajesh V. Thakker, Fadil Hannan, Brian Harding, Tara Moore, Treena Cranston, Sarah Howles, Nigel Rust, Paul T. Christie, Michael P. Whyte and Valerie Babinsky. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, Scientific Reports, Genomics, Journal of Bone and Mineral Research and Journal of Clinical Investigation.

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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