D G Barr

763 citations

28 papers · 530 indexed · h-index 14

Impact in

Genetics top 10%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders

Papers in

Developmental Biology 2
- Congenital limb and hand anomalies 2
Clinical Biochemistry 4
- Metabolism and Genetic Disorders 4

Co-authors: K.E. Buckton Michael F. Whitfield H F Stirling David T. Bonthron A Prader J. O. Forfar D. H. Shmerling S G Ratcliffe
Journals: Archives of Disease in Childhood (11 papers)Journal of Medical Genetics (4 papers)Acta Paediatrica (2 papers)Pediatric Research (2 papers)Journal of Thoracic and Cardiovascular Surgery (1 paper)
Partner nations: United Kingdom United States Switzerland

In The Last Decade

D G Barr

28 papers receiving 491 citations

Peers

Replace E A Werder with:

E A Werder Switzerland

Vincenzo Antona Italy

G. Fekete Hungary

María Juliana Ballesta‐Martínez Spain

Karen Chong Canada

Jean‐Louis Serre France

Tamara J. Gough Australia

Takeki Hirano Japan

Cheol Woo Ko South Korea

Peter Durie Canada

D G Barr relative to E A Werder Switzerland E A Werder's profile →

Citations per field

00.5×1.5×

E A Werder · 1×

×0.4 269/675

GENET

×0.8 37/47

CB

×1.0 35/34

NEPHR

×0.7 26/40

GASTR

×0.3 93/299

PPCH

Citations per year

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Countries citing papers authored by D G Barr

Since Specialization

Citations

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

Fields of papers citing papers by D G Barr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D G Barr. 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 G Barr. The network helps show where D G Barr may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Hyperammonaemia in critically ill septic infants Archives of Disease in Childhood ·P McEwan, David Simpson, J M Kirk, D G Barr, Kathryn J. McKenzie	2001	13
2	GNAS1 mutational analysis in pseudohypoparathyroidism Clinical Endocrinology ·S. F. Ahmed, Peter Dixon, David T. Bonthron, H F Stirling, D G Barr, C.J.H. Kelnar, Rajesh V. Thakker	1998	55
3	Neurogenic chronic idiopathic intestinal pseudo-obstruction, patent ductus arteriosus, and thrombocytopenia segregating as an X linked recessive disorder. Journal of Medical Genetics ·David Fitzpatrick, Lisa Strain, Alisalman Sheikh, D G Barr, Adam Todd, Nicholas M. Smith, W.G. Scobie	1997	18
4	Nager acrofacial dysostosis: minor familial manifestations supporting dominant inheritance Clinical Genetics ·David T. Bonthron, Roslizan Masripan, D G Barr	1993	11
5	Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency. Archives of Disease in Childhood ·D G Barr, Jeremy Kirk, Chalermpol Rudradawong, Ronald J. A. Wanders, R. B. H. Schutgens	1993	26
6	Parental consanguinity in the blepharophimosis, heart defect, hypothyroidism, mental retardation syndrome (Young-Simpson syndrome). Journal of Medical Genetics ·David T. Bonthron, Karen Barlow, Alvin M. Burt, D G Barr	1993	11
7	Outcome in tyrosinaemia type II. Archives of Disease in Childhood ·D G Barr, J M Kirk, Tao LIU	1991	10
8	Plasma Cyclic AMP Response to Intravenous Parathyroid Hormone in Pseudohypoparathyroidism Acta Paediatrica ·H F Stirling, J. A. B. Darling, D G Barr	1991	6
9	Familial growth hormone releasing factor deficiency in pseudopseudohypoparathyroidism. Archives of Disease in Childhood ·H F Stirling, D G Barr, C.J.H. Kelnar	1991	5
10	Ear, Nose and Throat Disorders in Children Archives of Disease in Childhood ·D G Barr	1986	2
11	Transient neonatal hyperparathyroidism secondary to maternal pseudohypoparathyroidism. Archives of Disease in Childhood ·В. Шведова, D G Barr	1981	29
12	Partial trisomy for long arm of chromosome 16. Journal of Medical Genetics ·K.E. Buckton, D G Barr	1981	24
13	A G‐band study of chromosomes in liveborn infants Annals of Human Genetics ·K.E. Buckton, M. L. O'RIORDAN, S G Ratcliffe, Joan Slight, Murray D. Mitchell, S. McBeath, A. J. Keay, D G Barr, M. Priscilla Short	1980	88
14	Catch-up Growth in Cortisone–Treated Rats: Effects of Calcium and Vitamin D Pediatric Research ·Nathaniel Bright Emerson, D G Barr, S J Pocock	1978	10
15	Hypophosphatasia: Enzyme Studies in Cultured Cells and Tissues Biochemical Society Transactions ·W. G. Brydon, Patricia M. Crofton, Nuñez Del Barrio H, D G Barr, R. A. Harkness	1975	16
16	Proceedings: Bone deficiency in Turner's syndrome measured by metacarpal dimensions. Archives of Disease in Childhood ·D G Barr	1974	12
17	Oral Calcium-loading Test in Rickets and in Neonatal Tetany: Effect of Vitamin D BMJ ·D G Barr, J. O. Forfar	1969	5
18	Oral Calcium-loading Test in Infancy, with Particular Reference to Idiopathic Hypercalcaemia BMJ ·D G Barr, J. O. Forfar	1969	25
19	INTRATHORACIC TUMORS ASSOCIATED WITH HYPOGLYCEMIA Journal of Thoracic and Cardiovascular Surgery ·Herbert C. Maier, D G Barr	1962	17
20	WATER DISTRIBUTION IN NORMAL SUBJECTS AND IN PATIENTS WITH LAËNNEC'S CIRRHOSIS Journal of Clinical Investigation ·H Gilder, S. Frank Redo, D G Barr, Charles G. Child	1954	19

About D G Barr

D G Barr is a scholar working on Developmental Biology, Clinical Biochemistry, Complementary and Manual Therapy, Genetics and Nephrology, having authored 28 papers that have together received 530 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (5 papers), Metabolism and Genetic Disorders (4 papers), Congenital heart defects research (4 papers), RNA regulation and disease (3 papers), Renal function and acid-base balance (2 papers), Peroxisome Proliferator-Activated Receptors (2 papers), Metabolism, Diabetes, and Cancer (2 papers) and Congenital limb and hand anomalies (2 papers). The work is most often cited by research in Genetics (269 citations), Clinical Biochemistry (37 citations), Nephrology (35 citations), Gastroenterology (26 citations) and Pediatrics, Perinatology and Child Health (93 citations). D G Barr has collaborated with scholars based in United Kingdom, United States and Switzerland. Frequent co-authors include K.E. Buckton, Michael F. Whitfield, H F Stirling, David T. Bonthron, A Prader, J. O. Forfar, D. H. Shmerling, S G Ratcliffe, S. McBeath and M. L. O'RIORDAN. Their work appears in journals such as Archives of Disease in Childhood, Journal of Medical Genetics, Acta Paediatrica, Pediatric Research and Journal of Thoracic and Cardiovascular Surgery.

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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