Detlef Knoll

624 total citations
11 papers, 119 citations indexed

About

Detlef Knoll is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, Detlef Knoll has authored 11 papers receiving a total of 119 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Clinical Biochemistry, 6 papers in Molecular Biology and 4 papers in Physiology. Recurrent topics in Detlef Knoll's work include Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (4 papers) and Diet and metabolism studies (4 papers). Detlef Knoll is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (4 papers) and Diet and metabolism studies (4 papers). Detlef Knoll collaborates with scholars based in New Zealand, South Africa and United States. Detlef Knoll's co-authors include Callum Wilson, Emma Glamuzina, Dianne Webster, Campbell Kyle, Carolus J. Reinecke, Roderick H.W. Simpson, P.J. Pretorius, H.S. Steyn, Lodewyk J. Mienie and Donald R. Love and has published in prestigious journals such as Journal of the Neurological Sciences, Journal of Inherited Metabolic Disease and Journal of Paediatrics and Child Health.

In The Last Decade

Detlef Knoll

11 papers receiving 116 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Detlef Knoll New Zealand	7	80	66	29	27	21	11	119
Patrícia Janeiro Portugal	8	89 1.1×	117 1.8×	31 1.1×	28 1.0×	44 2.1×	20	213
Mick Henderson United Kingdom	6	114 1.4×	100 1.5×	35 1.2×	21 0.8×	52 2.5×	6	175
Moeen Al-Sayed Saudi Arabia	6	70 0.9×	52 0.8×	23 0.8×	19 0.7×	20 1.0×	11	106
Marelle J. Bouva Netherlands	9	50 0.6×	24 0.4×	80 2.8×	9 0.3×	19 0.9×	20	221
Tomoko Tsuruoka Japan	8	131 1.6×	190 2.9×	11 0.4×	14 0.5×	13 0.6×	18	241
Keiko Ichimoto Japan	8	133 1.7×	220 3.3×	8 0.3×	14 0.5×	16 0.8×	22	267
Haya Alkhayyat United Kingdom	5	37 0.5×	51 0.8×	25 0.9×	9 0.3×	9 0.4×	7	103
Femke Molema Netherlands	7	136 1.7×	65 1.0×	38 1.3×	55 2.0×	24 1.1×	7	156
Melanie Downing United Kingdom	5	64 0.8×	32 0.5×	55 1.9×	16 0.6×	16 0.8×	7	125
Sarah Adam United Kingdom	6	76 0.9×	60 0.9×	7 0.2×	16 0.6×	66 3.1×	6	209

Countries citing papers authored by Detlef Knoll

Since Specialization

Citations

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

Fields of papers citing papers by Detlef Knoll

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Detlef Knoll. 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 Detlef Knoll. The network helps show where Detlef Knoll may publish in the future.

Co-authorship network of co-authors of Detlef Knoll

This figure shows the co-authorship network connecting the top 25 collaborators of Detlef Knoll. A scholar is included among the top collaborators of Detlef Knoll based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Detlef Knoll. Detlef Knoll is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

Glamuzina, Emma, et al.. (2022). The risk of classical galactosaemia in newborns with borderline galactose metabolites on newborn screening. JIMD Reports. 64(2). 180–186. 3 indexed citations

Heather, Natasha, et al.. (2022). Introducing Newborn Screening for Severe Combined Immunodeficiency—The New Zealand Experience. International Journal of Neonatal Screening. 8(2). 33–33. 10 indexed citations

Heather, Natasha, et al.. (2022). Introduction of a Protocol for Structured Follow-Up and Texting of Inadequate and Borderline-Positive Newborn Metabolic Screening Results. International Journal of Neonatal Screening. 8(2). 30–30. 2 indexed citations

Glamuzina, Emma, Dianne Webster, Detlef Knoll, et al.. (2022). Genotype–phenotype correlations in CPT1A deficiency detected by newborn screening in Pacific populations. JIMD Reports. 63(4). 322–329. 4 indexed citations

Wilson, Callum, et al.. (2019). The decision to discontinue screening for carnitine uptake disorder in New Zealand. Journal of Inherited Metabolic Disease. 42(1). 86–92. 28 indexed citations

Wilson, Callum, et al.. (2018). The decision to discontinue screening for carnitine uptake disorder in New Zealand. Journal of Inherited Metabolic Disease. 1 indexed citations

Wilson, Callum, et al.. (2016). The Risk of Fatty Acid Oxidation Disorders and Organic Acidemias in Children with Normal Newborn Screening. JIMD Reports. 35. 53–58. 7 indexed citations

Knoll, Detlef, Donald R. Love, Phillip Shepherd, et al.. (2016). The natural history of elevated tetradecenoyl‐L‐carnitine detected by newborn screening in New Zealand: implications for very long chain acyl‐CoA dehydrogenase deficiency screening and treatment. Journal of Inherited Metabolic Disease. 39(3). 409–414. 13 indexed citations

Glamuzina, Emma, et al.. (2011). Citrullinaemia type I: A common mutation in the Pacific Island population. Journal of Paediatrics and Child Health. 47(5). 262–265. 10 indexed citations

10.

Honey, Engela, et al.. (2003). Spondyloenchondromatosis with D-2-hydroxyglutaric aciduria: a report of a second patient with this unusual combination. Clinical Dysmorphology. 12(2). 95–99. 20 indexed citations

11.

Reinecke, Carolus J., Detlef Knoll, P.J. Pretorius, H.S. Steyn, & Roderick H.W. Simpson. (1985). The correlation between biochemical and histopathological findings in adrenoleukodystrophy. Journal of the Neurological Sciences. 70(1). 21–38. 21 indexed citations

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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