H Dahl

1.2k total citations
12 papers, 459 citations indexed

About

H Dahl is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, H Dahl has authored 12 papers receiving a total of 459 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Clinical Biochemistry and 4 papers in Genetics. Recurrent topics in H Dahl's work include Metabolism and Genetic Disorders (4 papers), Amino Acid Enzymes and Metabolism (3 papers) and Biochemical Acid Research Studies (3 papers). H Dahl is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Amino Acid Enzymes and Metabolism (3 papers) and Biochemical Acid Research Studies (3 papers). H Dahl collaborates with scholars based in Australia, United Kingdom and Austria. H Dahl's co-authors include R. M. Brown, Wendy Hutchison, G. K. Brown, Shireen R. Lamandé, William G. Cole, John F. Bateman, R. C. Iannello, Lise Lotte Hansen, Garry K. Brown and Greg Thompson and has published in prestigious journals such as Journal of Biological Chemistry, Annals of Neurology and Human Molecular Genetics.

In The Last Decade

H Dahl

12 papers receiving 448 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
H Dahl Australia	9	300	158	104	84	69	12	459
Wendy Hutchison Australia	13	540 1.8×	124 0.8×	302 2.9×	180 2.1×	55 0.8×	20	785
Majida Charif Morocco	17	417 1.4×	114 0.7×	88 0.8×	4 0.0×	167 2.4×	51	617
Sophie Devery United Kingdom	10	296 1.0×	111 0.7×	9 0.1×	8 0.1×	55 0.8×	17	418
Daniele Yumi Sunaga Brazil	9	201 0.7×	157 1.0×	13 0.1×	4 0.0×	5 0.1×	18	384
Arnold R. Rabin United States	10	333 1.1×	19 0.1×	29 0.3×	31 0.4×	8 0.1×	11	575
Shino Shimada Japan	15	315 1.1×	318 2.0×	33 0.3×	12 0.1×	3 0.0×	36	545
Janice C. Palumbos United States	8	245 0.8×	161 1.0×	9 0.1×	10 0.1×	32 0.5×	13	391
Jean-Louis Dufier France	8	236 0.8×	19 0.1×	5 0.0×	21 0.3×	90 1.3×	8	342
John Hildyard United Kingdom	12	775 2.6×	197 1.2×	46 0.4×	40 0.5×	2 0.0×	23	856
Katrin A. Mooslehner United Kingdom	10	297 1.0×	121 0.8×	9 0.1×	11 0.1×	2 0.0×	15	522

Countries citing papers authored by H Dahl

Since Specialization

Citations

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

Fields of papers citing papers by H Dahl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H Dahl

This figure shows the co-authorship network connecting the top 25 collaborators of H Dahl. A scholar is included among the top collaborators of H Dahl 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 H Dahl. H Dahl is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

Hitomi, Yuki, Erin L. Heinzen, Simona Donatello, et al.. (2013). Mutations in TNK2 in severe autosomal recessive infantile onset epilepsy. Annals of Neurology. 74(3). 496–501. 15 indexed citations

Houseman, Mark, Lucy Ellis, Alistair T. Pagnamenta, et al.. (2001). Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss. Journal of Medical Genetics. 38(1). 20–25. 75 indexed citations

Carlsson, Cynthia M., et al.. (1999). [Patients with diabetes search facts about their disease on the net. More information in Swedish is needed].. PubMed. 96(24). 2970–4. 1 indexed citations

Blok, Rozanne B., David R. Thorburn, Greg Thompson, & H Dahl. (1995). A topoisomerase II cleavage site is associated with a novel mitochondrial DNA deletion. Human Genetics. 95(1). 75–81. 33 indexed citations

Hutchison, Wendy & H Dahl. (1995). Detergent-enhanced sequencing of heat-denatured plasmid DNA.. PubMed. 19(4). 554–6. 1 indexed citations

Hansen, Lise Lotte, Garry K. Brown, R. M. Brown, & H Dahl. (1993). Pyruvate dehydrogenase deficiency caused by a 5 base pair duplication in the E1α subunit. Human Molecular Genetics. 2(6). 805–807. 8 indexed citations

Iannello, R. C. & H Dahl. (1992). Transcriptional Expression of a Testis-Specific Variant of the Mouse Pyruvate Dehydrogenase Elα Subunit1. Biology of Reproduction. 47(1). 48–58. 27 indexed citations

Petrovic, Vida, Steven Nasioulas, C.W. Chow, et al.. (1992). Minute Y chromosome derived marker in a child with gonadoblastoma: cytogenetic and DNA studies.. Journal of Medical Genetics. 29(8). 542–546. 29 indexed citations

Brown, Garry K., Robert Brown, H Dahl, et al.. (1990). Abstracts of papers presented at the Mammalian Genetics Group Meeting held in the Linnean Society Rooms, Piccadilly, London on 7 and 8 November 1989. Genetics Research. 55(2). 125–131. 1 indexed citations

10.

Dahl, H, et al.. (1990). A testis-specific form of the human pyruvate dehydrogenase E1α subunit is coded for by an intronless gene on chromosome 4. Genomics. 8(2). 225–232. 167 indexed citations

11.

Dahl, H, et al.. (1990). Pyruvate dehydrogenase deficiency caused by deletion of a 7-bp repeat sequence in the E1 alpha gene.. PubMed. 47(2). 286–93. 44 indexed citations

12.

Lamandé, Shireen R., H Dahl, William G. Cole, & John F. Bateman. (1989). Characterization of Point Mutations in the Collagen COL1A1 and COL1A2 Genes Causing Lethal Perinatal Osteogenesis Imperfecta. Journal of Biological Chemistry. 264(27). 15809–15812. 58 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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