C. E. Blank

1.5k total citations
37 papers, 1.1k citations indexed

About

C. E. Blank is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, C. E. Blank has authored 37 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 10 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in C. E. Blank's work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (5 papers) and Congenital limb and hand anomalies (3 papers). C. E. Blank is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (5 papers) and Congenital limb and hand anomalies (3 papers). C. E. Blank collaborates with scholars based in United Kingdom, India and Germany. C. E. Blank's co-authors include C. J. Dewhurst, R.R. Gordon, John Lorber, A. M. Potter, E.P. Evans, R.S.K. Chaganti, C. E. Ford, Paul R. Heath, B Griffiths and Diana Curtis and has published in prestigious journals such as Nature, The Lancet and BJOG An International Journal of Obstetrics & Gynaecology.

In The Last Decade

C. E. Blank

37 papers receiving 940 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
C. E. Blank United Kingdom	18	711	411	245	183	71	37	1.1k
de Grouchy J France	14	467 0.7×	375 0.9×	191 0.8×	182 1.0×	51 0.7×	103	854
M. Ray Canada	15	731 1.0×	391 1.0×	377 1.5×	292 1.6×	39 0.5×	36	1.1k
Mark W. Steele United States	24	846 1.2×	498 1.2×	323 1.3×	229 1.3×	44 0.6×	66	1.2k
S. Stengel‐Rutkowski Germany	20	835 1.2×	609 1.5×	424 1.7×	253 1.4×	79 1.1×	50	1.3k
Horace C. Thuline United States	21	706 1.0×	693 1.7×	193 0.8×	153 0.8×	24 0.3×	41	1.3k
PatriciaA. Jacobs United Kingdom	14	656 0.9×	510 1.2×	210 0.9×	143 0.8×	39 0.5×	21	1.3k
Jan Murken Germany	17	633 0.9×	535 1.3×	265 1.1×	261 1.4×	22 0.3×	51	1.1k
Dorothy Warburton United States	23	920 1.3×	549 1.3×	499 2.0×	331 1.8×	54 0.8×	35	1.5k
A Kleczkowska Belgium	22	1.1k 1.6×	490 1.2×	439 1.8×	346 1.9×	49 0.7×	80	1.3k
Elke Back Germany	15	576 0.8×	456 1.1×	138 0.6×	247 1.3×	25 0.4×	36	829

Countries citing papers authored by C. E. Blank

Since Specialization

Citations

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

Fields of papers citing papers by C. E. Blank

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C. E. Blank. 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 C. E. Blank. The network helps show where C. E. Blank may publish in the future.

Co-authorship network of co-authors of C. E. Blank

This figure shows the co-authorship network connecting the top 25 collaborators of C. E. Blank. A scholar is included among the top collaborators of C. E. Blank 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 C. E. Blank. C. E. Blank 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

Gläser, Birgitta, Eva Rossier, Gotthold Barbi, et al.. (2002). Molecular cytogenetic analysis of a constitutional de novo interstitial deletion of chromosome 12p in a boy with developmental delay and congenital anomalies. American Journal of Medical Genetics Part A. 116A(1). 66–70. 12 indexed citations

Parsons, M. A., et al.. (1992). The ocular pathology of Norrie disease in a fetus of 11 weeks' gestational age. Graefe s Archive for Clinical and Experimental Ophthalmology. 230(3). 248–251. 20 indexed citations

Curtis, Diana, et al.. (1989). Carrier detection and prenatal diagnosis in Norrie disease. Prenatal Diagnosis. 9(10). 735–740. 3 indexed citations

Curtis, Diana & C. E. Blank. (1989). Recombination between DXS7, DXS84 and a rare form of X-linked retinitis pigmentosa (McK-30 320). Human Genetics. 81(2). 200–202. 1 indexed citations

Kumar, Dheeraj & C. E. Blank. (1989). Early onset hereditary spinocerebellar ataxia: an autosomal recessive disorder distinct from Friedreich's ataxia.. PubMed. 26(10). 1014–9. 1 indexed citations

Curtis, Diana, et al.. (1988). An evaluation of reinforcement of genetic counselling on the consultand. Clinical Genetics. 33(4). 270–276. 4 indexed citations

Blank, C. E., et al.. (1983). Investigations for genotoxic effects after exposure to crude 2,4,5-trichlorophenol. Occupational and Environmental Medicine. 40(1). 87–91. 3 indexed citations

Blank, C. E.. (1978). Population Cytogenetics: Studies in Humans. Journal of Medical Genetics. 15(1). 81–82. 202 indexed citations

Cook, P.J.L., E.B. Robson, K.E. Buckton, et al.. (1978). Segregation of ABO, AK₁ and ACON_S in families with abnormalities of chromosome 9. Annals of Human Genetics. 41(3). 365–377. 33 indexed citations

10.

Blank, C. E.. (1976). Chromosome Variations in Human Evolution. Journal of Medical Genetics. 13(5). 413.2–414. 12 indexed citations

11.

Issa, Mahmoud Y., A. M. Potter, & C. E. Blank. (1976). Multiple congenital defects associated with trisomy for long arm of No. 4.. Journal of Medical Genetics. 13(4). 326–329. 14 indexed citations

12.

Owen, Leah A., Barbara A. Martin, C. E. Blank, & Faye R. Harris. (1974). Multiple congenital defects associated with trisomy for the short arm of chromosome 4. Journal of Medical Genetics. 11(3). 291–295. 14 indexed citations

13.

Blank, C. E., et al.. (1966). Sex Chromosome Abnormalities in Two State Hospitals for Patients requiring Special Security. Nature. 209(5023). 641–642. 92 indexed citations

14.

Blank, C. E., et al.. (1964). Chromosome Mosaicism in a Hermaphrodite. BMJ. 2(5401). 84.2–93. 11 indexed citations

15.

Blank, C. E.. (1964). SOME ASPECTS OF CHROMOSOME MOSAICISM IN CLINICAL MEDICINE. The Lancet. 284(7365). 903–906. 8 indexed citations

16.

Dewhurst, C. J., et al.. (1963). AN XY FEMALE WITH ABSENT GONADS AND VESTIGIAL PELVIC ORGANS. BJOG An International Journal of Obstetrics & Gynaecology. 70(4). 675–680. 21 indexed citations

17.

Blank, C. E., et al.. (1963). Chromosome Mosaicism in a Mongol Born to a Young Mother. Cytogenetic and Genome Research. 2(2-3). 76–85. 9 indexed citations

18.

Blank, C. E., et al.. (1962). HERITABLE VARIATION IN THE LENGTH OF THE Y CHROMOSOME. The Lancet. 280(7245). 18–20. 47 indexed citations

19.

Blank, C. E., et al.. (1962). Mosaicism in a Mother with a Mongol Child. PubMed. 2(5301). 378–380. 50 indexed citations

20.

Blank, C. E.. (1959). Apert's syndrome (a type of acrocephalosyndactyly)–observations on a British series of thirty‐nine cases*. Annals of Human Genetics. 24(2). 151–164. 218 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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