H. Telenius

3.2k citations

18 papers · 2.5k indexed · 1 hit paper · h-index 14

Molecular Biology top 5%
Genetics top 2%
Cellular and Molecular Neuroscience top 2%
Plant Science top 5%
Neurology top 5%

Co-authors: Nigel P. Carter Alan Tunnacliffe Bruce A.J. Ponder Michael R. Hayden Y. Paul Goldberg E. Almqvist B Kremer Susan E. Andrew
Topics: Genetic Neurodegenerative Diseases (8 papers)Mitochondrial Function and Pathology (5 papers)Neuroendocrine Tumor Research Advances (4 papers)
Cited by: Cellular and Molecular Neuroscience Genetics Neurology
Journals: Nature Nucleic Acids Research Human Molecular Genetics
Partner nations: Sweden United Kingdom Canada

In The Last Decade

H. Telenius

18 papers receiving 2.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer

1992 1.2k citations H. Telenius, Nigel P. Carter et al. Genomics profile →

Peers

Countries citing papers authored by H. Telenius

Since Specialization

Citations

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

Fields of papers citing papers by H. Telenius

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. Telenius

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

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Contribution of DNA Sequence and CAG Size to Mutation Frequencies of Intermediate Alleles for Huntington Disease: Evidence from Single Sperm Analyses 1997 ·Human Molecular Genetics ·Samuel S. Chong,E. Almqvist,H. Telenius,(unknown),K. Nichol,(unknown),Y. Paul Goldberg,Bassem R. Haddad,Fiona Richards,David Sillence,Cheryl R. Greenberg,Elizabeth Ives,Ger van den Engh,Mark Hughes,Michael R. Hayden	92
2	Somatic mosaicism in sperm is associated with intergenerational (CAG)_n changes in Huntington disease 1995 ·Human Molecular Genetics ·H. Telenius,E. Almqvist,B Kremer,Niamh Spence,Ferdinando Squitieri,K. Nichol,Ulla Grandell,(unknown),Caroline Benjamin,Imma Castaldo,Olga Calabrese,Maria Anvret,Y. Paul Goldberg,Michael R. Hayden	67
3	Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes. 1995 ·PubMed ·B Kremer,E. Almqvist,(unknown),Niamh Spence,H. Telenius,(unknown),Michael R. Hayden	107
4	DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence 1994 ·Human Molecular Genetics ·Ferdinando Squitieri,Susan E. Andrew,Y. Paul Goldberg,B Kremer,Niamh Spence,(unknown),K. Nichol,Jane Theilmann,Jacquie Greenberg,Jun Goto,Ichiro Kanazawa,J. Vesa,Leena Peltonen,E. Almqvist,Maria Anvret,H. Telenius,Binshan Lin,G. Napolitano,Kenneth Morgan,Michael R. Hayden	148
5	Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA. 1994 ·PubMed ·Elisabeth Blennow,H. Telenius,(unknown),Catharina Larsson,P. Henriksson,(unknown),(unknown),Magnus Nordenskjöld	70
6	Huntington disease without CAG expansion: phenocopies or errors in assignment? 1994 ·PubMed ·Susan E. Andrew,Y. Paul Goldberg,B Kremer,Ferdinando Squitieri,Jane Theilmann,Jutta Zeisler,H. Telenius,Shelin Adam,(unknown),Maria Anvret	82
7	Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic cases. 1993 ·Journal of Medical Genetics ·Y. Paul Goldberg,Susan E. Andrew,Jane Theilmann,B Kremer,Ferdinando Squitieri,H. Telenius,J.D. Brown,Michael R. Hayden	32
8	Preparation of chromosome‐specific paints and complete assignment of chromosomes in the pig flow karyotype 1993 ·Animal Genetics ·Cordelia F. Langford,Nigel Miller,Elizabeth M. Tucker,H. Telenius,Preben D. Thomsen	24
9	Molecular analysis of juvenile Huntington disease: the major influence on (CAG)_n repeat length is the sex of the affected parent 1993 ·Human Molecular Genetics ·H. Telenius,Hannie Kremer,(unknown),Susan E. Andrew,E. Almqvist,Maria Anvret,Cheryl R. Greenberg,Jacquie Greenberg,G Lucotte,(unknown),Amanda E. Starr,Y. Paul Goldberg,Michael R. Hayden	163
10	Molecular analysis of late onset Huntington's disease. 1993 ·Journal of Medical Genetics ·B Kremer,Ferdinando Squitieri,H. Telenius,Susan E. Andrew,Jane Theilmann,Niamh Spence,Y. Paul Goldberg,Michael R. Hayden	51
11	Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primerbreakdown → 1992 ·Genomics ·H. Telenius,Nigel P. Carter,(unknown),(unknown),Bruce A.J. Ponder,Alan Tunnacliffe	1158
12	Chromosome painting using chromosome-specific probes from flow-sorted pig chromosomes 1992 ·Cytogenetic and Genome Research ·Cordelia F. Langford,H. Telenius,(unknown),Nigel Miller,Elizabeth M. Tucker	18
13	Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics. 1992 ·Journal of Medical Genetics ·(unknown),M.A. Ferguson‐Smith,(unknown),H. Telenius,(unknown),M. Leversha,(unknown),Stephen Wood,(unknown),(unknown)	166
14	Application of linked DNA markers to screening families with multiple endocrine neoplasia type 2A. 1990 ·PubMed ·H. Telenius,Christopher G. Mathew,Yuichi Nakamura,D.F. Easton,(unknown),H. P. H. Neumann,Wolfgang Ziegler,Anna C. Schinzel,Bruce A.J. Ponder	6
15	Early diagnosis of multiple endocrine neoplasia type IIa 1989 ·Journal of Molecular Medicine ·Hartmut P.H. Neumann,Otto Müller,Bruce A.J. Ponder,Christopher G. Mathew,H. Telenius,W. Schempp,Carl Schuemichen,N. Freudenberg,P. Schollmeyer	2
16	BcII RFLP for the human vimentin gene 1988 ·Nucleic Acids Research ·(unknown),Barbara A. Smith,H. Telenius,Rudy M. Landsvater,C.H.C.M. Buys,Sérgio Ferrari,(unknown),Christopher G. Mathew	3
17	Exclusion of linkage of loci on chromosome 19 with multiple endocrine neoplasia, type 2 1987 ·Cytogenetic and Genome Research ·(unknown),D.F. Easton,Christopher G. Mathew,(unknown),H. Telenius,M. Telenius-Berg,(unknown)	10
18	A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10 1987 ·Nature ·Christopher G. Mathew,K. S. Chin,Douglas F. Easton,Karen L. Thorpe,(unknown),G. I. Liou,S.–L. Fong,C.D.B. Bridges,Harm R. Haak,A. C. Nieuwenhuijzen Kruseman,Søren Schifter,H. H. Hansen,H. Telenius,M. Telenius-Berg,Bruce A.J. Ponder	350

About H. Telenius

H. Telenius is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology, having authored 18 papers that have together received 2.5k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (8 papers), Mitochondrial Function and Pathology (5 papers) and Neuroendocrine Tumor Research Advances (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (698 citations), Genetics (1.0k citations) and Neurology (436 citations). H. Telenius has collaborated with scholars based in Sweden, United Kingdom and Canada. Frequent co-authors include Nigel P. Carter, Alan Tunnacliffe, Bruce A.J. Ponder, Michael R. Hayden, Y. Paul Goldberg, E. Almqvist, B Kremer, Susan E. Andrew, Niamh Spence and Maria Anvret. Their work appears in journals such as Nature, Nucleic Acids Research and Human Molecular Genetics.

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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