C. E. Blank

1.5k citations

37 papers · 1.1k indexed · h-index 18

Impact in

Developmental Biology top 5%
- Congenital limb and hand anomalies
Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research

Papers in ⓘ

Genetics 21
- Genomic variations and chromosomal abnormalities 11
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Dermatoglyphics and Human Traits 3
Molecular Biology 10
- Sexual Differentiation and Disorders 3
- Advanced biosensing and bioanalysis techniques 2

Co-authors: C. J. Dewhurst (5 shared papers)R.R. Gordon (2 shared papers)John Lorber (2 shared papers)A. M. Potter (2 shared papers)E.P. Evans (1 shared paper)C. E. Ford (1 shared paper)R.S.K. Chaganti (1 shared paper)Diana Curtis (4 shared papers)
Journals: Journal of Medical Genetics (11 papers)The Lancet (6 papers)Clinical Genetics (4 papers)Annals of Human Genetics (3 papers)Human Genetics (2 papers)
Partner nations: United Kingdom India Germany

In The Last Decade

C. E. Blank

37 papers receiving 940 citations

Peers

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-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 37 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Apert's syndrome (a type of acrocephalosyndactyly)–observations on a British series of thirty‐nine cases* Annals of Human Genetics ·C. E. Blank	1959	218
2	Population Cytogenetics: Studies in Humans Journal of Medical Genetics ·C. E. Blank	1978	202
3	Sex Chromosome Abnormalities in Two State Hospitals for Patients requiring Special Security Nature ·M. D. Casey, Leslie Segall, D. R. K. STREET, C. E. Blank	1966	92
4	Mosaicism in a Mother with a Mongol Child BMJ ·C. E. Blank, Emily Gemmell, M. D. Casey, M. Lord	1962	50
5	HERITABLE VARIATION IN THE LENGTH OF THE Y CHROMOSOME The Lancet ·Audrey Bishop, C. E. Blank, Henry Hunter	1962	47
6	XY SPERMATOCYTES IN AN XYY MALE The Lancet ·E.P. Evans, C. E. Ford, R.S.K. Chaganti, C. E. Blank, Henry Hunter	1970	39
7	Segregation of ABO, AK₁ and ACON_S in families with abnormalities of chromosome 9 Annals of Human Genetics ·P.J.L. Cook, E.B. Robson, K.E. Buckton, Clive A. Slaughter, J.E. Gray, C. E. Blank, Frelichowski James, M. A. C. Ridler, J Insley, M.A. Hultén	1978	33
8	CHROMOSOME COUNT IN A HERMAPHRODITE WITH SOME FEATURES OF KLINEFELTER'S SYNDROME The Lancet ·R.R. Gordon, F.J.P. O'Gorman, C. J. Dewhurst, C. E. Blank	1960	32
9	EXAMPLE OF XY/XO MOSAICISM The Lancet ·C. E. Blank, Audrey Bishop, J.P. Caley	1960	31
10	ATYPICAL TURNER SYNDROME The Lancet ·C. E. Blank, R.R. Gordon, Audrey Bishop	1961	24
11	Physical and mental defect of chromosomal origin in four individuals of the same family. Trisomy for the short arm of 9 Clinical Genetics ·C. E. Blank, D Colver, A. M. Potter, Jonathan B. McHugh, John Lorber	1975	24
12	AN XY FEMALE WITH ABSENT GONADS AND VESTIGIAL PELVIC ORGANS BJOG An International Journal of Obstetrics & Gynaecology ·C. J. Dewhurst, C. G. Paine, C. E. Blank	1963	21
13	The ocular pathology of Norrie disease in a fetus of 11 weeks' gestational age Graefe s Archive for Clinical and Experimental Ophthalmology ·M. A. Parsons, Diana Curtis, C. E. Blank, Howard Hughes, Alison McCartney	1992	20
14	Clinical manifestations of trisomy 5q. Journal of Medical Genetics ·D Kumar, Paul R. Heath, C. E. Blank	1987	20
15	Cornelia de Lange syndrome in several members of the same family. Journal of Medical Genetics ·Dilip Kumar, C. E. Blank, B Griffiths	1985	20
16	Interstitial deletion of the short arm of chromosome 5 in a mother and three children. Journal of Medical Genetics ·J L Walker, C. E. Blank, Barbara A. Smith	1984	19
17	An XO-X ring X chromosome mosaicism in an individual with normal secondary sexual development. Journal of Medical Genetics ·Audrey Bishop, C. E. Blank, K Simpson, C. J. Dewhurst	1966	17
18	A patient with 45,XX,Gminus-46,XX,Gr mosaicism. Journal of Medical Genetics ·C. E. Blank, John Lorber	1969	17
19	Multiple congenital defects associated with trisomy for long arm of No. 4. Journal of Medical Genetics ·Mahmoud Y. Issa, A. M. Potter, C. E. Blank	1976	14
20	Multiple congenital defects associated with trisomy for the short arm of chromosome 4 Journal of Medical Genetics ·Leah A. Owen, Barbara A. Martin, C. E. Blank, Faye R. Harris	1974	14

About C. E. Blank

C. E. Blank is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Developmental Biology and Plant Science, having authored 37 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Chromosomal and Genetic Variations (3 papers), Dermatoglyphics and Human Traits (3 papers), Congenital limb and hand anomalies (3 papers), Sexual Differentiation and Disorders (3 papers) and Advanced biosensing and bioanalysis techniques (2 papers). The work is most often cited by research in Developmental Biology (71 citations), Genetics (711 citations), Pediatrics, Perinatology and Child Health (245 citations), Reproductive Medicine (69 citations) and Molecular Biology (411 citations). C. E. Blank has collaborated with scholars based in United Kingdom, India and Germany. Frequent co-authors include C. J. Dewhurst, R.R. Gordon, John Lorber, A. M. Potter, E.P. Evans, C. E. Ford, R.S.K. Chaganti, Diana Curtis, B Griffiths and Paul R. Heath. Their work appears in journals such as Journal of Medical Genetics, The Lancet, Clinical Genetics, Annals of Human Genetics and Human Genetics.

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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