S.S. Papiha

660 total citations
26 papers, 515 citations indexed

About

S.S. Papiha is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, S.S. Papiha has authored 26 papers receiving a total of 515 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Pathology and Forensic Medicine and 5 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in S.S. Papiha's work include Forensic and Genetic Research (4 papers), Retinal Development and Disorders (4 papers) and Vitamin D Research Studies (3 papers). S.S. Papiha is often cited by papers focused on Forensic and Genetic Research (4 papers), Retinal Development and Disorders (4 papers) and Vitamin D Research Studies (3 papers). S.S. Papiha collaborates with scholars based in United Kingdom, Australia and India. S.S. Papiha's co-authors include Harish K. Datta, Roger M. Francis, B Pal, Satya S. Varanasi, R. M. Francis, Harish K. Datta, Christine Berger, Frances Harrington, Petros Perros and D. F. Roberts and has published in prestigious journals such as Annals of the Rheumatic Diseases, Journal of Clinical Pathology and Osteoporosis International.

In The Last Decade

S.S. Papiha

26 papers receiving 492 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
S.S. Papiha United Kingdom	14	194	162	116	89	61	26	515
Mila Jhamai Netherlands	10	250 1.3×	186 1.1×	204 1.8×	174 2.0×	30 0.5×	13	612
Makoto Hase Japan	8	321 1.7×	56 0.3×	44 0.4×	80 0.9×	42 0.7×	8	481
Abigail Samuels United Kingdom	10	199 1.0×	124 0.8×	23 0.2×	102 1.1×	28 0.5×	17	389
S.K. Abbas United Kingdom	11	259 1.3×	107 0.7×	30 0.3×	66 0.7×	16 0.3×	22	576
Hoda A. Hagrass Egypt	12	129 0.7×	73 0.5×	59 0.5×	39 0.4×	28 0.5×	16	386
Sakan Maeda Japan	11	148 0.8×	99 0.6×	57 0.5×	13 0.1×	47 0.8×	20	411
Hitoo Nakano Japan	12	202 1.0×	88 0.5×	57 0.5×	16 0.2×	58 1.0×	15	835
Mark E. Nuñes United States	12	202 1.0×	211 1.3×	59 0.5×	64 0.7×	10 0.2×	24	644
Tianbo Jin China	14	163 0.8×	52 0.3×	22 0.2×	137 1.5×	31 0.5×	35	474
Akiko Sada Japan	11	231 1.2×	45 0.3×	38 0.3×	29 0.3×	158 2.6×	31	563

Countries citing papers authored by S.S. Papiha

Since Specialization

Citations

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

Fields of papers citing papers by S.S. Papiha

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S.S. Papiha

This figure shows the co-authorship network connecting the top 25 collaborators of S.S. Papiha. A scholar is included among the top collaborators of S.S. Papiha 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 S.S. Papiha. S.S. Papiha 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

Varanasi, Satya S., R. M. Francis, Christine Berger, S.S. Papiha, & Harish K. Datta. (1999). Mitochondrial DNA Deletion Associated Oxidative Stress and Severe Male Osteoporosis. Osteoporosis International. 10(2). 143–149. 61 indexed citations

Papiha, S.S., et al.. (1999). Vitamin D Binding Protein Gene in Male Osteoporosis: Association of Plasma DBP and Bone Mineral Density with (TAAA)n-Alu Polymorphism in DBP. Calcified Tissue International. 65(4). 262–266. 32 indexed citations

Papiha, S.S., et al.. (1998). Age related somatic mitochondrial DNA deletions in bone.. Journal of Clinical Pathology. 51(2). 117–120. 26 indexed citations

Francis, Roger M., et al.. (1997). Vitamin D receptor gene polymorphism in men and its effect on bone density and calcium absorption. Clinical Endocrinology. 46(1). 83–86. 53 indexed citations

Malhotra, K. C., et al.. (1996). Population structure and genetic differentiation among 16 tribal populations of central India.. PubMed. 68(5). 679–705. 34 indexed citations

Papiha, S.S., Sarabjit Mastana, Niraj Singh, & D. F. Roberts. (1994). Khmers of Cambodia: A comparative genetic study of the populations of Southeast Asia. American Journal of Human Biology. 6(4). 465–479. 1 indexed citations

Bashir, R., C.F. Inglehearn, T J Keen, et al.. (1992). Exclusion of chromosome 6 and 8 locations in nonrhodopsin autosomal dominant retinitis pigmentosa families: Further locus heterogeneity in adRP. Genomics. 14(1). 191–193. 4 indexed citations

Munro, C.S., Sarabjit Mastana, & S.S. Papiha. (1992). Mapping of the Darier's disease gene by serogenetic markers: results in two large British kindreds.. PubMed. 35(3). 157–60. 3 indexed citations

Papiha, S.S., et al.. (1992). Association of Wegener's granulomatosis with HLA antigens and other genetic markers.. Annals of the Rheumatic Diseases. 51(2). 246–248. 43 indexed citations

10.

Papiha, S.S., et al.. (1991). Factor B (BF) Allotypes and Multiple Sclerosis in North-East England. Human Heredity. 41(6). 397–402. 5 indexed citations

11.

Inglehearn, C.F., M Jay, Douglas H. Lester, et al.. (1990). no evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): Evidence for genetic heterogeneity. Genomics. 6(1). 168–173. 28 indexed citations

12.

Inglehearn, Chris F., S.S. Papiha, M Jay, et al.. (1990). Linkage of internal minisatellite loci on chromosome 1 and exclusion of autosomal dominant retinitis pigmentosa proximal to rhesus.. Journal of Medical Genetics. 27(1). 14–16. 1 indexed citations

13.

Papiha, S.S., J. Boddy, D. F. Roberts, & David Bates. (1989). PHA-induced interferon in multiple sclerosis: association between gamma interferon and clinical and genetical variables. Acta Neurologica Scandinavica. 80(2). 145–150. 7 indexed citations

14.

Papiha, S.S., et al.. (1988). HLA Antigens in the Uitoto Indians and an Urban Population of Colombia. Human Heredity. 38(6). 337–340. 6 indexed citations

15.

Kendall‐Taylor, P., et al.. (1988). DIFFERENTIATION OF AUTOIMMUNE OPHTHALMOPATHY FROM GRAVES’HYPERTHYROIDISM BY ANALYSIS OF GENETIC MARKERS. Clinical Endocrinology. 28(6). 601–610. 35 indexed citations

16.

Papiha, S.S., B Pal, I D Griffiths, D. F. Roberts, & W. Carson Dick. (1988). GENETIC MARKERS IN SJOÖGREN'S SYNDROME: THE QUESTION OF ITS GENETIC HETEROGENEITY. Lara D. Veeken. 27(4). 265–274. 2 indexed citations

17.

Kendall‐Taylor, P., et al.. (1988). DIFFERENTIATION OF AUTOIMMUNE OPHTHALMOPATHY FROM GRAVES’ HYPERTHYROIDISM BY ANALYSIS OF GENETIC MARKERS. Clinical Endocrinology. 28(6). 601–610. 16 indexed citations

18.

Bernal, Jaime E., et al.. (1986). C3 Variants and Disease. Human Heredity. 36(2). 97–100. 4 indexed citations

19.

Papiha, S.S., Jerry S. Lanchbury, & B Pal. (1986). Genetic structure of the population with rheumatoid arthritis in north east England: a genetic approach to define different subtypes.. Annals of the Rheumatic Diseases. 45(11). 881–891. 5 indexed citations

20.

Papiha, S.S. & D. F. Roberts. (1975). Serum alkaline phosphatase in patients with multiple sclerosis. Clinical Genetics. 7(1). 77–82. 2 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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