Anna M. Kessling

2.5k citations

49 papers · 1.9k indexed · h-index 25

Impact in

Endocrinology, Diabetes and Metabolism top 2%
- Diabetes, Cardiovascular Risks, and Lipoproteins
Genetics top 5%
- Genetic Associations and Epidemiology

Papers in

Endocrinology, Diabetes and Metabolism 12
- Diabetes, Cardiovascular Risks, and Lipoproteins 11
Genetics 20
- Genetic Associations and Epidemiology 9
- Genomic variations and chromosomal abnormalities 5

Co-authors: Steve E. Humphries Jean Davignon Charles F. Sing Matthew J. Farrer Suzanne Lussier‐Cacan Bernhard Horsthemke Olivia Fletcher P.C. Barber
Journals: Human Genetics (11 papers)Annals of Human Genetics (3 papers)Atherosclerosis (3 papers)Clinical Genetics (3 papers)The Journal of Urology (2 papers)
Partner nations: United Kingdom Canada United States

In The Last Decade

Anna M. Kessling

49 papers receiving 1.9k citations

Peers

Countries citing papers authored by Anna M. Kessling

Since Specialization

Citations

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

Fields of papers citing papers by Anna M. Kessling

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna M. Kessling. 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 Anna M. Kessling. The network helps show where Anna M. Kessling may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Use of DNA Polymorphisms of the Apolipoprotein Genes to Study the Role of Genetic Variation in the Determination of Serum Lipid Levels Novartis Foundation symposium ·Steve E. Humphries, Philippa J. Talmud, Anna M. Kessling	2007	1
2	The Problem of Polygenic Disease Novartis Foundation symposium ·Robert Williamson, Anna M. Kessling	2007	1
3	EXPRESSION OF THE DEVELOPMENTAL AND ONCOGENIC PAX2 GENE IN HUMAN PROSTATE CANCER The Journal of Urology ·Bijan Khoubehi, Anna M. Kessling, J M Adshead, Gillian L. Smith, Daron Smith, C W Ogden	2001	7
4	Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome? Human Genetics ·Melisa J. Baptista, U. L. Fairbrother, C. Anthony Howard, Matthew J. Farrer, Gail E. Davies, Dimitra Trikka, Klio Maratou, Andrew N. Redington, Gottfried Greve, Pål R. Njølstad, Anna M. Kessling	2000	26
5	Variation in alphoid DNA size and trisomy 21: a possible cause of nondisjunction Human Genetics ·Klio Maratou, Yasmeen Siddique, Anna M. Kessling, Gail E. Davies	2000	11
6	A High-Resolution Physical Map of Human Chromosome 21p Using Yeast Artificial Chromosomes Genome Research ·Shengyue Wang, Marc Cruts, Jurgen Del‐Favero, Yi Zhang, Fadel Tissir, Marie-Claude Potier, David T. Patterson, Dean Nižetić, Assumpció Bosch, Haiming Chen, Lynda Bennett, Xavier Estivill, Anna M. Kessling, Stylianos E. Antonarakis, Christine Van Broeckhoven	1999	17
7	MTHFR association with arteriosclerotic vascular disease? Human Genetics ·Olivia Fletcher, Anna M. Kessling	1998	86
8	Human COL6A1: Genomic characterization of the globular domains, structural and evolutionary comparison with COL6A2 Mammalian Genome ·Dimitra Trikka, Tanja Davis, Vincenza Lapenta, C. Brahe, Anna M. Kessling	1997	7
9	Influence of genetic variability in the nondeletion LDL-receptor allele on phenotypic variation in French-Canadian familial hypercholesterolemia heterozygotes sharing a ‘null’ LDL-receptor gene defect Atherosclerosis ·Christine Bétard, Anna M. Kessling, Marie-Claude Roy, Jean Davignon	1996	21
10	Cladistic analysis of the apolipoprotein AI‐CIH‐AIV gene cluster using a healthy French Canadian sample. I. Haploid analysis Annals of Human Genetics ·Martha B. Haviland, Anna M. Kessling, Jean Davignon, Charles F. Sing	1995	12
11	Conserved gene sequences for species identification: PCR analysis of the 3′ UTR of the SON gene distinguishes human and other mammalian DNAs Forensic Science International ·B. Soteriou, Rosemary A. Fisher, Ilyas M. Khan, Anna M. Kessling, L. C. Archard, Laki Buluwela	1995	7
12	Genetic variation in the COL6A1 region is associated with congenital heart defects in trisomy 21 (Down's syndrome) Annals of Human Genetics ·Gail E. Davies, Catherine M. Howard, Matthew J. Farrer, Michelle M. Coleman, Lynda Bennett, Louise Cullen, Richard Wyse, John Burn, R. Williamson, Anna M. Kessling	1995	37
13	Polymorphisms and linkage disequilibrium in the COL6A1 and COL6A2 gene cluster: novel DNA polymorphisms in the region of a candidate gene for congenital heart defects in Down's syndrome Human Genetics ·Gail E. Davies, Catherine M. Howard, Lucy M. Gorman, Matthew J. Farrer, Anthony Holland, R. Williamson, Anna M. Kessling	1993	14
14	9 Diabetes secondary to genetic disorders Baillière s Clinical Endocrinology and Metabolism ·Stephen Robinson, Anna M. Kessling	1992	18
15	Molecular genetic evidence for a founder effect in familial hypercholesterolemia among French Canadians Human Genetics ·Christine Bétard, Anna M. Kessling, Marie-Claude Roy, Ann Chamberland, Suzanne Lussier‐Cacan, Jean Davignon	1992	54
16	A Phenocopy of Type III Dysbetalipoproteinemia Occurring in a Candidate Family for a Putative Apo E Receptor Defect Annals of Medicine ·Jean Davignon, Jean Dallongeville, Ghislaine O. Roederer, Madeleine Roy, Jean‐Charles Fruchart, Anna M. Kessling, D Bouthillier, Suzanne Lussier‐Cacan	1991	5
17	Genetic structure and the search for genotype-phenotype relationships: an example from disequilibrium in the Apo B gene region. Genetics ·Kim E. Zerba, Anna M. Kessling, Jean Davignon, Charles F. Sing	1991	26
18	Identification of a second “French Canadian” LDL receptor gene deletion and development of a rapid method to detect both deletions Clinical Genetics ·Yuanhong Ma, Christine Bétard, Madeleine Roy, Jean Davignon, Anna M. Kessling	1989	59
19	A PvuII polymorphism in the 5? flanking region of the apolipoprotein AIV gene: its use to study genetic variation determining serum lipid and apolipoprotein concentration Human Genetics ·Anna M. Kessling, Rohan Taylor, Anne Temple, Julie Hutson, Alicia Hidalgo, Steve E. Humphries	1988	23
20	A cladistic analysis of phenotype associations with haplotypes inferred from restriction endonuclease mapping. II. The analysis of natural populations. Genetics ·Alan R. Templeton, Charles F. Sing, Anna M. Kessling, Steve E. Humphries	1988	99

About Anna M. Kessling

Anna M. Kessling is a scholar working on Endocrinology, Diabetes and Metabolism, Genetics, Surgery, Immunology and Allergy and Molecular Biology, having authored 49 papers that have together received 1.9k indexed citations. Recurring topics across this work include Lipoproteins and Cardiovascular Health (17 papers), Diabetes, Cardiovascular Risks, and Lipoproteins (11 papers), Genetic Associations and Epidemiology (9 papers), Cholesterol and Lipid Metabolism (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Chromosomal and Genetic Variations (5 papers), RNA and protein synthesis mechanisms (4 papers) and Protein Kinase Regulation and GTPase Signaling (4 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (641 citations), Genetics (592 citations), Cancer Research (260 citations), Surgery (720 citations) and Physiology (282 citations). Anna M. Kessling has collaborated with scholars based in United Kingdom, Canada and United States. Frequent co-authors include Steve E. Humphries, Jean Davignon, Charles F. Sing, Matthew J. Farrer, Suzanne Lussier‐Cacan, Bernhard Horsthemke, Olivia Fletcher, P.C. Barber, Elizabeth Fisher and V. P. Prasher. Their work appears in journals such as Human Genetics, Annals of Human Genetics, Atherosclerosis, Clinical Genetics and The Journal of Urology.

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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