A.B. Lane

549 total citations
24 papers, 396 citations indexed

About

A.B. Lane is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, A.B. Lane has authored 24 papers receiving a total of 396 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Physiology. Recurrent topics in A.B. Lane's work include Lysosomal Storage Disorders Research (4 papers), Glycosylation and Glycoproteins Research (3 papers) and Metabolism and Genetic Disorders (3 papers). A.B. Lane is often cited by papers focused on Lysosomal Storage Disorders Research (4 papers), Glycosylation and Glycoproteins Research (3 papers) and Metabolism and Genetic Disorders (3 papers). A.B. Lane collaborates with scholars based in South Africa, United Kingdom and Papua New Guinea. A.B. Lane's co-authors include G.T. Nurse, T Jenkins, Trefor Jenkins, D. A. HOPKINSON, Arthur R. Rabson, Bharti Morar, Amanda Krause, Rinat Bernstein‐Molho, Colin Freeman and D. Whittaker and has published in prestigious journals such as The British Journal of Psychiatry, The Journal of Pediatrics and Clinica Chimica Acta.

In The Last Decade

A.B. Lane

23 papers receiving 356 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A.B. Lane South Africa	12	178	165	74	52	30	24	396
T. F. Wienker Germany	12	111 0.6×	259 1.6×	29 0.4×	46 0.9×	18 0.6×	18	385
J. Blicharska United States	7	57 0.3×	227 1.4×	27 0.4×	59 1.1×	46 1.5×	8	419
Thomas W. Hurley United States	14	121 0.7×	187 1.1×	48 0.6×	40 0.8×	27 0.9×	28	791
Osama K. Zaki Egypt	12	128 0.7×	200 1.2×	29 0.4×	102 2.0×	129 4.3×	33	454
Marie‐Anne Skomorowski Canada	14	65 0.4×	197 1.2×	94 1.3×	330 6.3×	24 0.8×	23	476
Derek Persons United States	6	55 0.3×	118 0.7×	62 0.8×	45 0.9×	6 0.2×	8	269
Gisela Machado-Oliveira United Kingdom	10	54 0.3×	200 1.2×	37 0.5×	52 1.0×	7 0.2×	12	528
Matthew F. Taylor United Kingdom	12	55 0.3×	199 1.2×	12 0.2×	44 0.8×	8 0.3×	18	515
Lois Isenman United States	10	56 0.3×	117 0.7×	37 0.5×	51 1.0×	6 0.2×	14	336
Α. Gravanis Greece	10	64 0.4×	163 1.0×	34 0.5×	39 0.8×	10 0.3×	14	407

Countries citing papers authored by A.B. Lane

Since Specialization

Citations

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

Fields of papers citing papers by A.B. Lane

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A.B. Lane. 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 A.B. Lane. The network helps show where A.B. Lane may publish in the future.

Co-authorship network of co-authors of A.B. Lane

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

All Works

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20 of 20 papers shown

Lane, A.B.. (2013). STR null alleles complicate parentage testing in South Africa. South African Medical Journal. 103(12). 1004–1004. 5 indexed citations

Hobbs, Angela, et al.. (2012). Chitotriosidase Deficiency: A Mutation Update in an African Population. JIMD Reports. 10. 11–16. 9 indexed citations

Heitner, René, et al.. (2009). Glucocerebrosidase gene mutations in black South Africans with Gaucher disease. Blood Cells Molecules and Diseases. 43(1). 129–133. 8 indexed citations

Lane, A.B.. (2007). The nature of tri-allelic TPOX genotypes in African populations. Forensic Science International Genetics. 2(2). 134–137. 25 indexed citations

Lane, A.B., et al.. (2002). Genetic substructure in South African Bantu‐speakers: Evidence from autosomal DNA and Y‐chromosome studies. American Journal of Physical Anthropology. 119(2). 175–185. 44 indexed citations

Jenkins, T, et al.. (1999). The molecular basis of transferase galactosaemia in South African negroids. Journal of Inherited Metabolic Disease. 22(1). 37–42. 25 indexed citations

Lane, A.B., et al.. (1997). The molecular characterization of Gaucher disease in South Africa. Early Human Development. 49(3). 241–241. 1 indexed citations

Morar, Bharti & A.B. Lane. (1996). The molecular characterization of Gaucher disease in South Africa. Clinical Genetics. 50(2). 78–84. 12 indexed citations

Collinge, Janelle E., Lynn E. DeLisi, A. Boccio, et al.. (1991). Evidence for a Pseudo-autosomal Locus for Schizophrenia Using the Method of Affected Sibling Pairs. The British Journal of Psychiatry. 158(5). 624–629. 49 indexed citations

10.

Krause, Amanda, A.B. Lane, & T Jenkins. (1988). A new high activity plasma cholinesterase variant.. Journal of Medical Genetics. 25(10). 677–681. 18 indexed citations

11.

Krause, Amanda, A.B. Lane, & T Jenkins. (1987). Pseudocholinesterase variation in southern African populations.. PubMed. 71(5). 298–301. 2 indexed citations

12.

Hart, Stephen L., A.B. Lane, & T Jenkins. (1986). Partial adenosine deaminase deficiency: another family from southern Africa. Human Genetics. 74(3). 307–12. 3 indexed citations

13.

Lane, A.B.. (1985). On the nature of l-xylulose reductase deficiency in essential pentosuria. Biochemical Genetics. 23(1-2). 61–72. 15 indexed citations

14.

Lane, A.B., et al.. (1980). Segregation of Tay-Sachs and Sandhoff alleles in a non-Jewish family.. PubMed. 32(6). 920–6. 1 indexed citations

15.

Jenkins, T, A.B. Lane, G.T. Nurse, & D. A. HOPKINSON. (1979). Red cell adenosine deaminase (ADA) polymorphism in Southern Africa, with special reference to ADA deficiency among the !Kung. Annals of Human Genetics. 42(4). 425–433. 15 indexed citations

16.

Lane, A.B. & Trefor Jenkins. (1978). Two variant hexosaminidase β-chain alleles segregating in a South African family. Clinica Chimica Acta. 87(2). 219–228. 16 indexed citations

17.

Jenkins, Trefor, Arthur R. Rabson, G.T. Nurse, A.B. Lane, & D. A. HOPKINSON. (1976). Deficiency of adenosine deaminase not associated with severe combined immunodeficiency. The Journal of Pediatrics. 89(5). 732–736. 63 indexed citations

18.

Nurse, G.T., A.B. Lane, & Trefor Jenkins. (1976). Sero-genetic studies on the Dama of South West Africa. Annals of Human Biology. 3(1). 33–50. 20 indexed citations

19.

Jenkins, Trefor, A.B. Lane, G.T. Nurse, & Jiro Tanaka. (1975). Sero-Genetic Studies on the G/wi and G//ana San of Botswana. Human Heredity. 25(4). 318–328. 6 indexed citations

20.

Balinsky, Doris, et al.. (1974). G6PD kuanyama: a new variant of human erythrocyte glucose-6-phosphate dehydrogenase showing slower than normal electrophoretic mobility.. PubMed. 39(1). 5–13. 3 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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