M. Preus

1.3k total citations
44 papers, 966 citations indexed

About

M. Preus is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, M. Preus has authored 44 papers receiving a total of 966 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 11 papers in Molecular Biology and 7 papers in Pathology and Forensic Medicine. Recurrent topics in M. Preus's work include Connective tissue disorders research (6 papers), Dermatoglyphics and Human Traits (5 papers) and Metabolism and Genetic Disorders (4 papers). M. Preus is often cited by papers focused on Connective tissue disorders research (6 papers), Dermatoglyphics and Human Traits (5 papers) and Metabolism and Genetic Disorders (4 papers). M. Preus collaborates with scholars based in Canada, United States and France. M. Preus's co-authors include F. Clarke Fraser, Ségolène Aymé, John M. Opitz, Judith Allanson, James F. Reynolds, Judith G. Hall, Helen E. Hughes, James F. Reynolds, Michel Vekemans and Paige Kaplan and has published in prestigious journals such as The Journal of Pediatrics, Journal of Autism and Developmental Disorders and Journal of Medical Genetics.

In The Last Decade

M. Preus

44 papers receiving 908 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Preus Canada	19	443	412	149	122	102	44	966
N R Dennis United Kingdom	20	793 1.8×	628 1.5×	231 1.6×	98 0.8×	91 0.9×	32	1.3k
D Donnai United Kingdom	14	576 1.3×	447 1.1×	146 1.0×	70 0.6×	225 2.2×	22	1.2k
I. T. Thomas United States	15	551 1.2×	273 0.7×	107 0.7×	131 1.1×	142 1.4×	25	846
Robert F. Stratton United States	19	916 2.1×	736 1.8×	44 0.3×	353 2.9×	108 1.1×	42	1.4k
de Grouchy J France	14	467 1.1×	375 0.9×	17 0.1×	191 1.6×	78 0.8×	103	854
Fryns Jp Belgium	16	728 1.6×	399 1.0×	18 0.1×	297 2.4×	108 1.1×	106	996
Élodie Gautier France	10	206 0.5×	449 1.1×	320 2.1×	98 0.8×	54 0.5×	19	1.1k
Iosif W. Lurie United States	23	1.1k 2.4×	730 1.8×	39 0.3×	590 4.8×	287 2.8×	72	1.6k
Stephanie Spranger Germany	14	606 1.4×	509 1.2×	19 0.1×	80 0.7×	70 0.7×	34	860
Suzanna G.M. Frints Netherlands	21	1.1k 2.4×	878 2.1×	43 0.3×	416 3.4×	95 0.9×	39	1.9k

Countries citing papers authored by M. Preus

Since Specialization

Citations

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

Fields of papers citing papers by M. Preus

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

Küster, Wolfgang, et al.. (1987). Alopecia, macular degeneration, and growth retardation: A new syndrome?. American Journal of Medical Genetics. 28(2). 477–481. 2 indexed citations

Allanson, Judith, et al.. (1986). Noonan Syndrome. Obstetrical & Gynecological Survey. 41(1). 44–45. 2 indexed citations

Aymé, Ségolène, M. Preus, John M. Opitz, & James F. Reynolds. (1986). Spondylocostal/spondylothoracic dysostosis: The clinical basis for prognosticating and genetic counseling. American Journal of Medical Genetics. 24(4). 599–606. 43 indexed citations

Cortés, Fanny, Yves Lacassie, F. Clarke Fraser, & M. Preus. (1986). An unusal case of ectodermal dysplasia. American Journal of Medical Genetics. 25(2). 289–291. 3 indexed citations

Eronen, Marianne, et al.. (1985). New syndrome: A digito‐reno‐cerebral syndrome. American Journal of Medical Genetics. 22(2). 281–285. 12 indexed citations

Preus, M., et al.. (1985). A PROGNOSTIC SCORE FOR Graves' DISEASE. Clinical Endocrinology. 23(6). 653–661. 9 indexed citations

Preus, M., et al.. (1984). Trisomy 9 (pter → q1 to q3): the phenotype as an objective aid to karyotypic interpretation. Clinical Genetics. 26(1). 52–55. 2 indexed citations

Preus, M.. (1984). Differential diagnosis of the Williams and the Noonan syndromes. Clinical Genetics. 25(5). 429–434. 24 indexed citations

Preus, M., Christopher J. Linstrom, Polomeno Rc, & Jean Milot. (1983). Waardenburg syndrome—penetrance of major signs. American Journal of Medical Genetics. 15(3). 383–388. 13 indexed citations

10.

Preus, M., F C Fraser, & F. W. Wiglesworth. (1983). An oculocerebral hypopigmentation syndrome.. PubMed. 31(4). 323–8. 13 indexed citations

11.

Preus, M., et al.. (1983). Definition and diagnosis of the Brachmann–De Lange syndrome. American Journal of Medical Genetics. 16(3). 301–312. 49 indexed citations

12.

Preus, M.. (1980). The numerical versus intuitive approach to syndrome nosology.. PubMed. 16(5). 93–104. 13 indexed citations

13.

MacGibbon, Brenda & M. Preus. (1979). The distorted shell method for clustering for syndrome classification.. PubMed. 31(4). 498–507. 3 indexed citations

14.

Preus, M., et al.. (1977). Familial occurrence of the Williams syndrome. The Journal of Pediatrics. 91(4). 614–616. 22 indexed citations

15.

Preus, M.. (1977). Renal Anomalies and Oligohydramnios in the Cerebro-oculofacio-skeletal Syndrome. Archives of Pediatrics and Adolescent Medicine. 131(1). 62–62. 21 indexed citations

16.

Preus, M., Mordechai Feingold, & F. Clarke Fraser. (1975). Internipple distance and hand measurements in various syndromes.. PubMed. 11(5). 3–6. 1 indexed citations

17.

Preus, M.. (1975). Iris pattern in patients with the Williams syndrome. The Journal of Pediatrics. 87(5). 840–840. 4 indexed citations

18.

Preus, M. & F. Clarke Fraser. (1974). The Cerebro‐Oculo‐Facio‐Skeletal syndrome. Clinical Genetics. 5(4). 294–297. 30 indexed citations

19.

Preus, M. & F. Clarke Fraser. (1971). Genetics of hereditary nephropathy with deafness (Alport's disease). Clinical Genetics. 2(6). 331–337. 18 indexed citations

20.

Preus, M., F. Clarke Fraser, & E Lévy. (1970). Dermatoglyphics in Congenital Heart Malformations. Human Heredity. 20(4). 388–402. 9 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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