M. H. K. Shokeir

1.9k total citations · 1 hit paper
48 papers, 1.3k citations indexed

About

M. H. K. Shokeir is a scholar working on Molecular Biology, Genetics and Nutrition and Dietetics. According to data from OpenAlex, M. H. K. Shokeir has authored 48 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Genetics and 8 papers in Nutrition and Dietetics. Recurrent topics in M. H. K. Shokeir's work include Trace Elements in Health (7 papers), Genetic Neurodegenerative Diseases (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). M. H. K. Shokeir is often cited by papers focused on Trace Elements in Health (7 papers), Genetic Neurodegenerative Diseases (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). M. H. K. Shokeir collaborates with scholars based in Canada, United States and Egypt. M. H. K. Shokeir's co-authors include Sérgio D.J. Pena, Donald C. Shreffler, Nathan L. Kobrinsky, John M. Opitz, K. L. Ying, Laurence Brownell, C S Houston, Hardally R. Hegde, James F. Reynolds and Wendy S. Meschino and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Neurology.

In The Last Decade

M. H. K. Shokeir

48 papers receiving 1.2k citations

Hit Papers

PRIMARY SEX-RATIO AND SIZE OF FAMILY 1970 2026 1988 2007 1970 50 100 150 200 250
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.

  1. PRIMARY SEX-RATIO AND SIZE OF FAMILY
    1970 284 citations M. H. K. Shokeir The Lancet profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. H. K. Shokeir Canada 19 557 355 191 178 175 48 1.3k
Meinhard Robinow United States 21 781 1.4× 599 1.7× 243 1.3× 229 1.3× 116 0.7× 70 1.7k
F. A. Beemer Netherlands 28 1.0k 1.9× 637 1.8× 179 0.9× 301 1.7× 185 1.1× 73 2.0k
L.I. Al-Gazali United Arab Emirates 22 691 1.2× 553 1.6× 178 0.9× 207 1.2× 201 1.1× 60 1.5k
R. Neil Schimke United States 27 882 1.6× 699 2.0× 418 2.2× 207 1.2× 146 0.8× 76 2.4k
L. A. Sandkuyl Netherlands 18 550 1.0× 297 0.8× 111 0.6× 72 0.4× 182 1.0× 29 1.1k
Harold F. Falls United States 24 1.0k 1.8× 478 1.3× 128 0.7× 77 0.4× 67 0.4× 50 2.0k
H. Minaguchi Japan 26 476 0.9× 250 0.7× 126 0.7× 131 0.7× 79 0.5× 111 2.0k
William K. Rashbaum United States 22 675 1.2× 108 0.3× 110 0.6× 220 1.2× 184 1.1× 52 1.9k
Renata Laxová United States 19 765 1.4× 623 1.8× 157 0.8× 289 1.6× 90 0.5× 53 1.6k
R Rappaport France 30 857 1.5× 645 1.8× 341 1.8× 509 2.9× 271 1.5× 129 2.5k

Countries citing papers authored by M. H. K. Shokeir

Since Specialization
Citations

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

Fields of papers citing papers by M. H. K. Shokeir

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. H. K. Shokeir

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

All Works

20 of 20 papers shown
1.
2.
Stevenson, Roger E., J. Fernando Arena, Alice Gibson, et al.. (1998). Renpenning Syndrome Maps to Xp11. The American Journal of Human Genetics. 62(5). 1092–1101. 26 indexed citations
3.
Adam, Shelin, S Wiggins, Maurice Bloch, et al.. (1993). Five year study of prenatal testing for Huntington's disease: demand, attitudes, and psychological assessment.. Journal of Medical Genetics. 30(7). 549–556. 67 indexed citations
4.
Ang, Lee Cyn, et al.. (1991). Leigh’s Disease with Clinical Manifestations of Cornelia de Lange Syndrome. Pediatric Neurosurgery. 17(4). 192–195. 3 indexed citations
5.
Pearce, W G, et al.. (1987). Autosomal recessive juvenile cataract in Hutterites. Ophthalmic Paediatrics and Genetics. 8(2). 119–124. 10 indexed citations
6.
Shokeir, M. H. K.. (1978). Complete trisomy 22. Clinical Genetics. 14(3). 139–146. 12 indexed citations
7.
Shokeir, M. H. K.. (1978). Expression of “adult” polycystic renal disease in the fetus and newborn. Clinical Genetics. 14(2). 61–72. 41 indexed citations
8.
Pagon, Roberta A, et al.. (1978). ACHOO syndrome (autosomal dominant compelling helio-ophthalmic outburst syndrome).. PubMed. 14(6B). 361–3. 16 indexed citations
9.
Shokeir, M. H. K.. (1977). Universal permanent alopecia, psychomotor epilepsy, pyorrhea and mental subnormality. Clinical Genetics. 11(1). 13–17. 15 indexed citations
10.
Pena, Sérgio D.J. & M. H. K. Shokeir. (1974). Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: A lethal condition. The Journal of Pediatrics. 85(3). 373–375. 128 indexed citations
11.
Shokeir, M. H. K., et al.. (1974). Autosomal recessive cerebro-oculo-facioskeletal (COFS) syndrome. The Journal of Pediatrics. 84(6). 913–913. 17 indexed citations
12.
Pena, Sérgio D.J. & M. H. K. Shokeir. (1974). Autosomal recessive Cerebro‐Oculo‐Facio‐Skeletal (COFS) syndrome. Clinical Genetics. 5(4). 285–293. 85 indexed citations
13.
Shokeir, M. H. K.. (1971). Hypoplastic left heart syndrome: An autosomal recessive disorder. Clinical Genetics. 2(1). 7–14. 18 indexed citations
14.
Shokeir, M. H. K., et al.. (1971). Asphyxiating thoracic chondrodystrophy. Association with renal disease and evidence for possile heterozygous expression.. Journal of Medical Genetics. 8(1). 107–112. 24 indexed citations
15.
Shokeir, M. H. K.. (1971). Biochemical and immunological characterization of ceruloplasmin genetic variants. Clinical Genetics. 2(1). 41–49. 4 indexed citations
16.
Shokeir, M. H. K.. (1971). Investigations on the nature of ceruloplasmin deficiency in the newborn. Clinical Genetics. 2(4). 223–227. 14 indexed citations
17.
Shokeir, M. H. K.. (1970). PRIMARY SEX-RATIO AND SIZE OF FAMILY. The Lancet. 295(7640). 245–245. 284 indexed citations breakdown →
18.
Shokeir, M. H. K.. (1970). Quantitative variation in serum ceruloplasmin among ethnic groups. Clinical Genetics. 1(3-4). 166–170. 8 indexed citations
19.
Shokeir, M. H. K.. (1968). ORAL CONTRACEPTIVES AND CÆRULOPLASMIN ACTIVITY. The Lancet. 292(7579). 1192–1192. 7 indexed citations
20.
Shokeir, M. H. K.. (1968). COITAL FREQUENCY AND DOWN'S SYNDROME. The Lancet. 292(7577). 1081–1081. 8 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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