S. E. Olpin

6.7k citations

81 papers · 3.0k indexed · h-index 31

Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders 64
Biochemistry top 2%
Molecular Biology top 5%
- Mitochondrial Function and Pathology 33
- Biochemical and Molecular Research 11
- Peroxisome Proliferator-Activated Receptors 8
Rheumatology top 5%
- Folate and B Vitamins Research 9
Physiology top 5%
- Diet and metabolism studies 8
Pediatrics, Perinatology and Child Health
- Neonatal Health and Biochemistry 12
Cell Biology
- Muscle metabolism and nutrition 9

Co-authors: N. T. Davies N. J. Manning R. J. Pollitt Brage Storstein Andresen Neyaz Alam Morteza Pourfarzam Chris Bates Niels Gregersen
Cited by: Clinical Biochemistry Biochemistry Molecular Biology
Journals: Journal of Inherited Metabolic Disease (25 papers)Molecular Genetics and Metabolism (4 papers)The American Journal of Human Genetics (3 papers)
Partner nations: United Kingdom United States Denmark

In The Last Decade

S. E. Olpin

81 papers receiving 2.9k citations

Peers

Countries citing papers authored by S. E. Olpin

Since Specialization

Citations

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

Fields of papers citing papers by S. E. Olpin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. E. Olpin. 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 S. E. Olpin. The network helps show where S. E. Olpin may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Biochemical assessment of patients following ketogenic diets for epilepsy: Current practice in the UK and Ireland Epilepsia Open ·Natasha E. Schoeler,LU Xiao-xiang,I.Yu. Aleksandrova,Chang-gyum Kim,A. Bandati,ANGIE STEFANNY TICONA GONZALES,Kirsty J Martin-McGill,S. E. Olpin,Fiona Ivison	2019	5
2	Recurrent rhabdomyolysis caused by carnitine palmitoyltransferase II deficiency, common but under-recognised: Lessons to be learnt Molecular Genetics and Metabolism Reports ·Meena Balasubramanian,Thomas M. Jenkins,Richard Kirk,I. M. Nesbitt,S. E. Olpin,八大澤村,Godfrey T. Gillett	2018	11
3	A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency Human Genetics ·Charlotte L. Alston,Abdrabo Abu Saileek,Emma L. Blakely,Monika Oláhová,Langping He,Colin J. McMahon,S. E. Olpin,Iain P. Hargreaves,Cheuk Ka Leong,Robert McFarland,P Goffrini,Maureen J. O’Sullivan,Robert W. Taylor	2015	40
4	Recurrent Ventricular Tachycardia in Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency JIMD Reports ·Paulina Bala,Sacha Ferdinandusse,S. E. Olpin,P Chetcuti,A. A. M. Morris	2015	1
5	Determinants of urinary methylmalonic acid concentration in an elderly population in the United Kingdom American Journal of Clinical Nutrition ·Laura Silvestri,Jonna Aili,Kurt L. Schroeter,N. J. Manning,S. E. Olpin,Margo E. Barker,Hilary J. Powers	2012	13
6	A Vitamin B-12 Supplement of 500 μg/d for Eight Weeks Does Not Normalize Urinary Methylmalonic Acid or Other Biomarkers of Vitamin B-12 Status in Elderly People with Moderately Poor Vitamin B-12 Status Journal of Nutrition ·Marilyn Hill,Laura Silvestri,Margo E. Barker,Jonna Aili,N. J. Manning,S. E. Olpin,Stuart J. Moat,Jean Russell,Hilary J. Powers	2012	22
7	Glutaric aciduria type 1 in South Africa—high incidence of glutaryl-CoA dehydrogenase deficiency in black South Africans Molecular Genetics and Metabolism ·Gail-Ann P. Wilson,E. Owen,Peter Berman,Hongqi Wang,Oluwabosoye Abitoye,S. E. Olpin,N. J. Manning,Ingrid Baumgarten,Felicity Leisegang,Howard Henderson	2010	37
8	Interstitial deletion of 1p22.2p31.1 and medium‐chain acyl‐CoA dehydrogenase deficiency in a patient with global developmental delay American Journal of Medical Genetics Part A ·Gustavo Maegawa,Diane M. Freeman,Brage Storstein Andresen,S. E. Olpin,周水根,Joe T.R. Clarke,Ikuko Teshima	2008	10
9	Phosphoserine Aminotransferase Deficiency: A Novel Disorder of the Serine Biosynthesis Pathway The American Journal of Human Genetics ·R. Johnson,Valérie Race,Younès Achouri,Elsa Wiame,Mark Sharrard,S. E. Olpin,Aditi,James R. Bonham,Jaak Jaeken,Gert Matthijs,Emile Van Schaftingen	2007	89
10	ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency Brain ·Rikke Katrine Jentoft Olsen,S. E. Olpin,Brage Storstein Andresen,Z Miedzybrodzka,Morteza Pourfarzam,B. Merinero,Frank E. Frerman,Michael W. Beresford,John Dean,Nanna Cornelius,Oluf Andersen,Anders Oldfors,Elisabeth Holme,Niels Gregersen,Douglass M. Turnbull,Andrew A.M. Morris	2007	215
11	Genetic Basis for Correction of Very-Long-Chain Acyl–Coenzyme A Dehydrogenase Deficiency by Bezafibrate in Patient Fibroblasts: Toward a Genotype-Based Therapy The American Journal of Human Genetics ·SALAH MAACHE,Fatima Djouadi,Flore Aubey,S. E. Olpin,Brage Storstein Andresen,Seiji Yamaguchi,Hanna Mandel,Toshiyuki Fukao,Jos P.N. Ruiter,Ronald J. A. Wanders,R.P. McAndrew,瀬戸優樹,Jean Bastin	2007	54
12	Failure to repair the c.338C>T mutation in carnitine palmitoyl transferase 2 deficient skin fibroblasts using chimeraplasty Molecular Genetics and Metabolism ·Y. Vargas-Luna,S. E. Olpin,Ann Dalton,Nick Bishop,Peter Grabowski	2007	1
13	Consensus case definitions for MCADD among infants with presumptive positive newborn screening results Journal of Inherited Metabolic Disease ·Nadeem Pasha,A. Kaczynski,Abdullaev Farxod Ozodovich,Morteza Pourfarzam,Mr Hitesh,M. Downing,Romana Gajdošová,Reshma Sri Matthi,Brage Storstein Andresen,S. E. Olpin,Carol Dezateux	2006	1
14	The Use of [9,10-3H]Myristate, [9,10-3H]Palmitate and [9,10-3H]Oleate for the Detection and Diagnosis of Medium and Long-Chain Fatty Acid Oxidation Disorders in Intact Cultured Fibroblasts Kluwer Academic Publishers eBooks ·S. E. Olpin,N. J. Manning,R. J. Pollitt,James R. Bonham,M. Downing,Geo. N. Carter	2006	15
15	Clinical Features of Multiple Cutaneous and Uterine Leiomyomatosis Archives of Dermatology ·Neyaz Alam,Ella Barclay,Andrew Rowan,Jonathan P. Tyrer,Eduardo Calonje,Sanjiv Manek,David P. Kelsell,Irene M. Leigh,S. E. Olpin,Ian Tomlinson	2005	127
16	Fumarate hydratase mutations and predisposition to cutaneous leiomyomas, uterine leiomyomas and renal cancer British Journal of Dermatology ·Neyaz Alam,S. E. Olpin,I.M. Leigh	2005	94
17	Implications of impaired ketogenesis in fatty acid oxidation disorders Prostaglandins Leukotrienes and Essential Fatty Acids ·S. E. Olpin	2004	30
18	Lethal Cardiac Tachyarrhythmia in a Patient with Neonatal Carnitine-Acylcarnitine Translocase Deficiency Pediatric and Developmental Pathology ·Karen Choong,Joe T.R. Clarke,E. Cutz,Bárbara Vargas Zambrana,S. E. Olpin	2001	10
19	A patient with carnitine-acylcarnitine translocase deficiency with a mild phenotype The Journal of Pediatrics ·A. A. M. Morris,S. E. Olpin,M. Brivet,Douglass M. Turnbull,Richard A. Jones,J. V. Leonard	1998	34
20	Prenatal diagnosis of glutathione synthase deficiency Prenatal Diagnosis ·N. J. Manning,Norman Davies,S. E. Olpin,Kevin Carpenter,M. F. Smith,R. J. Pollitt,Sheila L. B. Duncan,Agne Larsson,Birgit Carlsson	1994	7

About S. E. Olpin

S. E. Olpin is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology, having authored 81 papers that have together received 3.0k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (64 papers), Mitochondrial Function and Pathology (33 papers), Neonatal Health and Biochemistry (12 papers), Biochemical and Molecular Research (11 papers), Muscle metabolism and nutrition (9 papers), Folate and B Vitamins Research (9 papers), Diet and metabolism studies (8 papers) and Peroxisome Proliferator-Activated Receptors (8 papers). The work is most often cited by research in Clinical Biochemistry (1.5k citations), Biochemistry (238 citations) and Molecular Biology (1.9k citations). S. E. Olpin has collaborated with scholars based in United Kingdom, United States and Denmark. Frequent co-authors include N. T. Davies, N. J. Manning, R. J. Pollitt, Brage Storstein Andresen, Neyaz Alam, Morteza Pourfarzam, Chris Bates, Niels Gregersen, I.M. Leigh and Werner J.H. Koopman. Their work appears in journals such as Journal of Inherited Metabolic Disease, Molecular Genetics and Metabolism, The American Journal of Human Genetics, British Journal Of Nutrition and Journal of Clinical Pathology.

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