M. Andrew Nesbit

5.5k citations

99 papers · 4.2k · h-index 32

Impact in

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

Papers in

Nephrology 21
- Parathyroid Disorders and Treatments 20
Molecular Biology 47
- Congenital heart defects research 11
- CRISPR and Genetic Engineering 8
- RNA Interference and Gene Delivery 7

Co-authors: Rajesh V. Thakker (44 shared papers)Fadil M. Hannan (19 shared papers)Brian N Harding (9 shared papers)Treena Cranston (9 shared papers)Tara Moore (32 shared papers)Sarah Howles (8 shared papers)Nigel A. Rust (6 shared papers)Michael P. Whyte (8 shared papers)
Journals: The Journal of Clinical Endocrinology & Metabolism (10 papers)Scientific Reports (5 papers)Human Molecular Genetics (5 papers)Journal of Bone and Mineral Research (4 papers)Genomics (4 papers)
Partner nations: United Kingdom United States Denmark

In The Last Decade

M. Andrew Nesbit

96 papers receiving 4.0k 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

Showing the 20 most-cited of 99 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	GATA3 haplo-insufficiency causes human HDR syndrome Nature ·Hilde Van Esch, Peter M. A. Groenen, M. Andrew Nesbit, Simone Schuffenhauer, Peter Lichtner, Gert Vanderlinden, Brian N Harding, Rolf Beetz	2000	501
2	Mutations Affecting G-Protein Subunit α 11 in Hypercalcemia and Hypocalcemia New England Journal of Medicine ·M. Andrew Nesbit, Fadil M. Hannan, Sarah Howles, Valerie N. Babinsky, Rosie A. Head, Treena Cranston, Nigel A. Rust, Maurine R. Hobbs	2013	306
3	Factors influencing success of clinical genome sequencing across a broad spectrum of disorders Nature Genetics ·Jenny C. Taylor, Hilary C. Martin, Stefano Lise, John Broxholme, Jean‐Baptiste Cazier, Andy Rimmer, Alexander A Kanapin, Gerton A. Lunter	2015	291
4	Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3 Nature Genetics ·M. Andrew Nesbit, Fadil M. Hannan, Sarah Howles, Adam J. Reed, Treena Cranston, Clare E Thakker, Lorna Gregory, Andrew J. Rimmer	2012	226
5	Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites Human Molecular Genetics ·Fadil M. Hannan, M. Andrew Nesbit, Chenyi Zhang, Treena Cranston, Alan Curley, Brian N Harding, Carl Fratter, Nigel A. Rust	2012	157
6	Characterization of GATA3 Mutations in the Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) Syndrome Journal of Biological Chemistry ·M. Andrew Nesbit, Michael R. Bowl, Brian N Harding, Asif Ali, Alejandro Raul Ayala, Carol A. Crowe, Angus Dobbie, Geeta Hampson	2004	144
7	Activating calcium-sensing receptor mutation in the mouse is associated with cataracts and ectopic calcification Proceedings of the National Academy of Sciences ·Tertius Hough, Debora Bogani, Michael T Cheeseman, Jack Favor, M. Andrew Nesbit, Rajesh V. Thakker, Mary Frances Lyon	2004	120
8	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 N Harding, Elaine R. Levy, Andrew Jefferson, Emanuela Valeria Volpi, Karine Rizzoti, Robin Howard Lovell-Badge	2005	119
9	Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor Human Molecular Genetics ·Asif Ali, P. T. Christie, I. V. Grigorieva, Brian N Harding, Hilde Van Esch, S. F. Ahmed, Maria A. K. Bitner-Glindzicz, EBERHARD BLIND	2006	116
10	Whole-Exome Sequencing Studies of Nonhereditary (Sporadic) Parathyroid Adenomas The Journal of Clinical Endocrinology & Metabolism ·Paul J. Newey, M. Andrew Nesbit, Andrew J. Rimmer, Moustafa Attar, Paul T. Christie, Caroline M. Gorvin, Michael Stechman, Lorna Gregory	2012	113
11	CRISPR/Cas9 DNA cleavage at SNP-derived PAM enables both in vitro and in vivo KRT12 mutation-specific targeting Gene Therapy ·David Courtney, Jonathan E. Moore, Sarah D. Atkinson, Eleonora Maurizi, Edwin H. A. Allen, Deena M. Leslie Pedrioli, W.H. Irwin McLean, M. Andrew Nesbit	2015	106
12	Gata3-deficient mice develop parathyroid abnormalities due to dysregulation of the parathyroid-specific transcription factor Gcm2 Journal of Clinical Investigation ·I. V. Grigorieva, Samantha M. Mirczuk, Katherine U. Gaynor, M. Andrew Nesbit, Elena F. Grigorieva, Qiaozhi Wei, Asif Ali, Rebecca J. Fairclough	2010	104
13	MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMDMO) Journal of Clinical Investigation ·Ann M. Kennedy, Masaki Inada, Stephen M. Krane, Paul T. Christie, Brian N Harding, Carlos López-Otı́n, Luis Sánchez‐Pulido, Anna A. J. Pannett	2005	91
14	Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype–phenotype correlations, codon bias and dominant-negative effects Human Molecular Genetics ·Fadil M. Hannan, Sarah Howles, Angela Rogers, Treena Cranston, Caroline M. Gorvin, Valerie N. Babinsky, Adam J. Reed, Clare E. Thakker	2015	69
15	Whole-Exome Sequencing Studies of Nonfunctioning Pituitary Adenomas The Journal of Clinical Endocrinology & Metabolism ·Paul J. Newey, M. Andrew Nesbit, Andrew J. Rimmer, Rosie A. Head, Caroline M. Gorvin, Moustafa Attar, Lorna Gregory, John A. H. Wass	2013	68
16	Towards personalised allele-specific CRISPR gene editing to treat autosomal dominant disorders Scientific Reports ·Kathleen A. Christie, David Courtney, Larry DeDionisio, Connie Chao-Shern, Shyamasree De Majumdar, Laura Mairs, M. Andrew Nesbit, Tara Moore	2017	68
17	Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene Nature Clinical Practice Endocrinology &#38 Metabolism ·Fadil M. Hannan, M. Andrew Nesbit, Paul T. Christie, Carl Fratter, Nicholas E Dudley, Greg Sadler, Rajesh V. Thakker	2007	67
18	Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy JCI Insight ·Caroline M. Gorvin, Fadil M. Hannan, Sarah Howles, Valerie N. Babinsky, Siân E. Piret, Angela Rogers, Andrew J. Freidin, Michelle E. Stewart	2017	61
19	The Calcilytic Agent NPS 2143 Rectifies Hypocalcemia in a Mouse Model With an Activating Calcium-Sensing Receptor (CaSR) Mutation: Relevance to Autosomal Dominant Hypocalcemia Type 1 (ADH1) Endocrinology ·Fadil M. Hannan, Gerard V. Walls, Valerie N. Babinsky, M. Andrew Nesbit, Enikö Kállay, Tertius Hough, William Duncan Fraser, Roger Cox	2015	60
20	CLC-5 and KIF3B interact to facilitate CLC-5 plasma membrane expression, endocytosis, and microtubular transport: relevance to pathophysiology of Dent's disease American Journal of Physiology-Renal Physiology ·Adam J. Reed, Nellie Y. Loh, Sara Terryn, Jonathan D. Lippiat, Chris Partridge, Juris Galvanovskis, Siân E. Williams, François Jouret	2009	58

About M. Andrew Nesbit

M. Andrew Nesbit is a scholar working on Nephrology, Molecular Biology, Genetics, Radiology, Nuclear Medicine and Imaging and Physiology, having authored 99 papers that have together received 4.2k indexed citations. Recurring topics across this work include Parathyroid Disorders and Treatments (20 papers), Congenital heart defects research (11 papers), Erythrocyte Function and Pathophysiology (9 papers), Corneal surgery and disorders (9 papers), CRISPR and Genetic Engineering (8 papers), RNA Interference and Gene Delivery (7 papers), Connective tissue disorders research (7 papers) and Genetic Syndromes and Imprinting (7 papers). The work is most often cited by research in Nephrology (1.3k citations), Genetics (1.1k citations), Molecular Biology (2.0k citations), Oncology (466 citations) and Sensory Systems (85 citations). M. Andrew Nesbit has collaborated with scholars based in United Kingdom, United States and Denmark. Frequent co-authors include Rajesh V. Thakker, Fadil M. Hannan, Brian N Harding, Treena Cranston, Tara Moore, Sarah Howles, Nigel A. Rust, Michael P. Whyte, Valerie N. Babinsky and Paul T. Christie. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, Scientific Reports, Human Molecular Genetics, Journal of Bone and Mineral Research and Genomics.

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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M. Andrew Nesbit

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