D. Gardner‐Medwin

4.6k citations

111 papers · 3.4k indexed · h-index 33

Impact in

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Genetics top 2%
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders

Papers in

Clinical Biochemistry 10
- Metabolism and Genetic Disorders 10
Genetics 13
- Neurogenetic and Muscular Disorders Research 11

Co-authors: Kate Bushby P. Hudgson L. V. B. Nicholson J. N. Walton R. J. Pennington K. Bushby Mark A. Johnson John Burn
Journals: Journal of the Neurological Sciences (21 papers)Developmental Medicine & Child Neurology (16 papers)Journal of Medical Genetics (10 papers)Archives of Disease in Childhood (6 papers)Neurology (5 papers)
Partner nations: United Kingdom United States India

In The Last Decade

D. Gardner‐Medwin

105 papers receiving 3.2k citations

Peers

Replace F. Cornelio with:

F. Cornelio Italy

Lucía Morandi Italy

Beril Talim Türkiye

Thomas Voït Germany

John T. Sladky United States

P. Hudgson United Kingdom

Betty Q. Banker United States

Morten Dunø Denmark

Hirofumi Komaki Japan

Emma Ciafaloni United States

D. Gardner‐Medwin relative to F. Cornelio Italy F. Cornelio's profile →

Citations per field

00.5×1.6×

F. Cornelio · 1×

×1.4 374/277

CB

×1.4 581/414

GENET

×1.1 2k/2k

MB

×1.5 544/356

CMN

×1.6 569/357

CCM

Citations per year

2016

2017

2018

2019

2020

2021

2022

2023

2024

2025

Countries citing papers authored by D. Gardner‐Medwin

Since Specialization

Citations

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

Fields of papers citing papers by D. Gardner‐Medwin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D. Gardner‐Medwin. 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 D. Gardner‐Medwin. The network helps show where D. Gardner‐Medwin may publish in the future.

Co-authors

The 25 scholars most cited alongside D. Gardner‐Medwin, 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 D. Gardner‐Medwin Line = papers co-authored together D. Gardner‐Medwin links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Tethering of the vertebral artery in the congenital arcuate foramen of the atlas vertebra: a possible cause of vertebral artery dissection in children Developmental Medicine & Child Neurology ·A. Auerbach, Lara Ferreira Magalhães, D. Gardner‐Medwin, Nick Todd, A. Gholkar, P S Baxter, Suharshi Gupta Sikander Chairag	2001	16
2	Tethering of the vertebral artery in the congenital arcuate foramen of the atlas vertebra: a possible cause of vertebral artery dissection in children Developmental Medicine & Child Neurology ·A. Auerbach, Lara Ferreira Magalhães, D. Gardner‐Medwin, N. V. Todd, A. Gholkar, P S Baxter, E Kamińska	2001	66
3	PYRIDOXINE‐DEPENDENT SEIZURES: DEMOGRAPHIC, CLINICAL, MRI AND PSYCHOMETRIC FEATURES, AND EFFECT OF DOSE ON INTELLIGENCE QUOTIENT Developmental Medicine & Child Neurology ·Peter Baxter, Peter Griffiths, Thomas M. Kelly, D. Gardner‐Medwin	1996	84
4	Vigabatrin monotherapy in resistant neonatal seizures Seizure ·Peter Baxter, D. Gardner‐Medwin, D D Barwick, Paul G. Ince, John H. Livingston, Deborah Murdoch‐Eaton	1995	14
5	The Radiological Features of Hemimegalencephaly Including Three Cases Associated with Proteus Syndrome Neuropediatrics ·Peter Griffiths, Freidrich C. Luft, D. Gardner‐Medwin, A. Gholkar, V. L. McAllister	1994	50
6	The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy Journal of Neurology ·Kate Bushby, D. Gardner‐Medwin	1993	140
7	Variability in clinical, genetic and protein abnormalities in manifesting carriers of Duchenne and Becker muscular dystrophy Neuromuscular Disorders ·Kate Bushby, Judith A. Goodship, L. V. B. Nicholson, Mark Johnson, S. S. Ford, D. Gardner‐Medwin	1993	50
8	HEAD CIRCUMFERENCE AND INTELLECTUAL PERFORMANCE OF PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY Developmental Medicine & Child Neurology ·Richard Appleton, K. Bushby, D. Gardner‐Medwin, John L. Welch, Paul J. Kelly	1991	22
9	Intracranial Calcification and Seizures: a Case of Central Neurofibromatosis Developmental Medicine & Child Neurology ·Scott Chadwick, William H. Church, D. Gardner‐Medwin, Raj Sengupta	1990	1
10	Heterogeneity of dystrophin expression in patients with Duchenne and Becker muscular dystrophy Acta Neuropathologica ·L. V. B. Nicholson, Mark A. Johnson, D. Gardner‐Medwin, S.S. Bhattacharya, J.B. Harris	1990	127
11	Abnormalities of carbohydrate metabolism and of oct gene function in the Rett syndrome Brain and Development ·Angus Clarke, D. Gardner‐Medwin, А.А. Симушина, Kathleen E. Smith, Duffy C. Murphy, Kevin Carpenter, Shomi S. Bhattacharya, Abdulmaged Musa Ali Alghithy, J Fleetwood, A Aynsley‐Green	1990	12
12	Dystrophin in skeletal muscle II. Immunoreactivity in patients with Xp21 muscular dystrophy Journal of the Neurological Sciences ·L. V. B. Nicholson, Keith Davison, Margaret A. Johnson, Clarke R. Slater, Carol Young, 鐘湘庭, D. Gardner‐Medwin, John B. Harris	1989	116
13	Familial intermittent ataxia due to a defect of the E1 component of pyruvate dehydrogenase complex Journal of the Neurological Sciences ·Laurence A. Bindoff, MA Birch-Machin, UNICEF, D. Gardner‐Medwin, J. Gordon Lindsay, Douglass M. Turnbull	1989	19
14	Some studies of the duchenne and autosomal recessive types of muscular dystrophy Brain and Development ·D. Gardner‐Medwin, Mário Fernando Simões Guerra	1989	17
15	Multiple chromosome rearrangements in a childhood ependymoma Cancer Genetics and Cytogenetics ·N Bown, A D Pearson, E. V. Davison, D. Gardner‐Medwin, P J Crawford, Robert Perry	1988	19
16	A trial of flunarizine in the treatment of duchenne muscular dystrophy Muscle & Nerve ·D J Dick, D. Gardner‐Medwin, Kholoud A. Elnakma, Mary Gibson, Judy M. Simpson, Timothy J. Walls	1986	17
17	Diaphragmatic paralysis due to spinal muscular atrophy. An unrecognised cause of respiratory failure in infancy? Archives of Disease in Childhood ·Robert McWilliam, D. Gardner‐Medwin, Daniel Doyle, John B.P. Stephenson	1985	19
18	CLINICAL FEATURES AND CLASSIFICATION OF THE MUSCULAR DYSTROPHIES British Medical Bulletin ·D. Gardner‐Medwin	1980	100
19	Children with genetic muscular disorders. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·D. Gardner‐Medwin	1977	6
20	Two Cases of Cryptococcal Meningitis, one Treated with 5-Fluorocytosine BMJ ·Joseph Treat, M. J. Campbell, D. Gardner‐Medwin, H. R. Ingham, I. G. Murray	1969	30

About D. Gardner‐Medwin

D. Gardner‐Medwin is a scholar working on Clinical Biochemistry, Genetics, Molecular Biology, Cellular and Molecular Neuroscience and Neurology, having authored 111 papers that have together received 3.4k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (38 papers), Genetic Neurodegenerative Diseases (13 papers), Neurogenetic and Muscular Disorders Research (11 papers), Metabolism and Genetic Disorders (10 papers), Adipose Tissue and Metabolism (9 papers), Mitochondrial Function and Pathology (9 papers), Cardiomyopathy and Myosin Studies (8 papers) and Nuclear Structure and Function (7 papers). The work is most often cited by research in Clinical Biochemistry (374 citations), Genetics (581 citations), Molecular Biology (2.2k citations), Cellular and Molecular Neuroscience (544 citations) and Cardiology and Cardiovascular Medicine (569 citations). D. Gardner‐Medwin has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include Kate Bushby, P. Hudgson, L. V. B. Nicholson, J. N. Walton, R. J. Pennington, K. Bushby, Mark A. Johnson, John Burn, J.B. Harris and K. Hall. Their work appears in journals such as Journal of the Neurological Sciences, Developmental Medicine & Child Neurology, Journal of Medical Genetics, Archives of Disease in Childhood and Neurology.

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.

Explore authors with similar magnitude of impact