M. Crocker

527 total citations
16 papers, 245 citations indexed

About

M. Crocker is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, M. Crocker has authored 16 papers receiving a total of 245 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in M. Crocker's work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). M. Crocker is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). M. Crocker collaborates with scholars based in United Kingdom, Greece and Canada. M. Crocker's co-authors include Matthew Campbell, Leona T. Campbell, S. B. COGHILL, B.M. Cattanach, Ian Craig, Helen Stewart, A. Boon, Jon Jonasson, M Fitchett and Henk Giele and has published in prestigious journals such as Nature, Human Genetics and American Journal of Medical Genetics.

In The Last Decade

M. Crocker

16 papers receiving 206 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Crocker United Kingdom	9	183	88	68	52	25	16	245
Amelia Villa Spain	9	176 1.0×	83 0.9×	75 1.1×	50 1.0×	23 0.9×	12	241
J Philip Denmark	6	183 1.0×	129 1.5×	53 0.8×	56 1.1×	33 1.3×	13	302
Frank S. Grass United States	8	184 1.0×	88 1.0×	122 1.8×	84 1.6×	9 0.4×	12	256
Catherine Metaxotou Greece	12	188 1.0×	130 1.5×	140 2.1×	66 1.3×	10 0.4×	35	334
Paula R. Martens United States	11	216 1.2×	118 1.3×	100 1.5×	91 1.8×	8 0.3×	15	280
Erin B. Kaminsky United States	3	182 1.0×	107 1.2×	39 0.6×	75 1.4×	19 0.8×	3	201
G. R. Stalder Switzerland	12	256 1.4×	146 1.7×	98 1.4×	87 1.7×	7 0.3×	21	387
Milly Andrle Austria	7	239 1.3×	191 2.2×	72 1.1×	195 3.8×	7 0.3×	11	358
Anne Bazin France	8	119 0.7×	74 0.8×	90 1.3×	42 0.8×	5 0.2×	16	195
Sorrell H. Waxman United States	13	217 1.2×	132 1.5×	143 2.1×	50 1.0×	34 1.4×	19	387

Countries citing papers authored by M. Crocker

Since Specialization

Citations

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

Fields of papers citing papers by M. Crocker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Crocker

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

All Works

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16 of 16 papers shown

Stewart, Helen, Sarah Smalley, M. Crocker, et al.. (2008). Congenital disseminated neurofibromatosis type 1: A clinical and molecular case report. American Journal of Medical Genetics Part A. 146A(11). 1444–1452. 7 indexed citations

Babbs, Christian, Raoul Heller, David B. Everman, et al.. (2007). A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation. Human Genetics. 122(2). 191–199. 19 indexed citations

Crocker, M., et al.. (2006). Cryptic mosaicism for monosomy 20 identified in renal tract cells. Clinical Genetics. 70(3). 228–232. 17 indexed citations

Crocker, M., et al.. (2004). A chromosome 21‐derived minute marker in a mosaic trisomy 21 background: Implications for risk assessments in marker chromosome cases. American Journal of Medical Genetics Part A. 127A(2). 191–193. 15 indexed citations

Crocker, M., et al.. (2002). Prenatal diagnosis of cri du chat (5p‐) syndrome in association with isolated moderate bilateral ventriculomegaly. Prenatal Diagnosis. 22(1). 64–66. 16 indexed citations

Campbell, Leona T., et al.. (2001). Phenotypic effects of balanced X-autosome translocations in females: a retrospective survey of 104 cases reported from UK laboratories. Human Genetics. 108(4). 318–327. 57 indexed citations

Boyd, Patricia A., et al.. (1995). Maternal 3;13 chromosome insertion, with severe pre‐eclampsia. Clinical Genetics. 47(1). 17–21. 9 indexed citations

Crocker, M., et al.. (1990). A sibship with Roberts/SC phocomelia syndrome. American Journal of Medical Genetics. 37(1). 18–22. 7 indexed citations

Crocker, M., et al.. (1988). An unbalanced autosomal translocation (7;9) associated with feminization. Clinical Genetics. 34(1). 70–73. 38 indexed citations

10.

Wolstenholme, Jane, M. Crocker, & Jon Jonasson. (1988). A study of chromosomal aberrations in amniotic fluid cell cultures. Prenatal Diagnosis. 8(5). 339–353. 6 indexed citations

11.

Crocker, M., Jon Jonasson, & Chirag Patel. (1985). An unusual case of X‐15 translocation: evidence for the presence of an ‘activator’ region on Xpter of Man. Clinical Genetics. 28(6). 556–560. 2 indexed citations

12.

Crocker, M. & Ian Craig. (1983). Variation in regulation of steroid sulphatase locus in mammals. Nature. 303(5919). 721–722. 20 indexed citations

13.

Crocker, M.. (1982). Metaphase I delay as a factor influencing translocation yield from spermatogonial irradiation in mice carrying Robertsonian translocations. Mutation Research Letters. 103(3-6). 339–343. 5 indexed citations

14.

Crocker, M. & B.M. Cattanach. (1981). X-ray induction of translocations in mice carrying metacentrics (Robertsonian fusions); Detection of whole arm chromosome exchanges. Mutation Research Letters. 91(4-5). 353–357. 15 indexed citations

15.

Cattanach, B.M., et al.. (1979). An attempt to distinguish a modified genetic response of the mouse testis to X-ray exposure by the action of a spermatologonial chalone. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 62(1). 197–201. 5 indexed citations

16.

Crocker, M. & B.M. Cattanach. (1979). The genetics ofSleek: a possible regulatory mutation of thetabby-crinkled-downlesssyndrome. Genetics Research. 34(3). 231–238. 7 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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