Martine Borghgraef

1.3k total citations
54 papers, 925 citations indexed

About

Martine Borghgraef is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Martine Borghgraef has authored 54 papers receiving a total of 925 indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Genetics, 15 papers in Molecular Biology and 14 papers in Cognitive Neuroscience. Recurrent topics in Martine Borghgraef's work include Genetics and Neurodevelopmental Disorders (30 papers), Autism Spectrum Disorder Research (14 papers) and Genomic variations and chromosomal abnormalities (7 papers). Martine Borghgraef is often cited by papers focused on Genetics and Neurodevelopmental Disorders (30 papers), Autism Spectrum Disorder Research (14 papers) and Genomic variations and chromosomal abnormalities (7 papers). Martine Borghgraef collaborates with scholars based in Belgium, Netherlands and United States. Martine Borghgraef's co-authors include J. P. Fryns, Herman Van den Berghe, Jean‐Pierre Fryns, Jean Steyaert, Eric Legius, A. M. Wiegers, L.M.G. Curfs, Annick Vogels, Gene S. Fisch and Mie‐Jef Descheemaeker and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Autism and Developmental Disorders and Journal of Medical Genetics.

In The Last Decade

Martine Borghgraef

52 papers receiving 891 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martine Borghgraef Belgium 18 780 408 381 84 76 54 925
David S. Hong United States 19 649 0.8× 385 0.9× 317 0.8× 48 0.6× 73 1.0× 51 1.1k
Thomas L. Baumgardner United States 12 645 0.8× 706 1.7× 288 0.8× 73 0.9× 56 0.7× 15 1.0k
Diane C. Lanham United States 11 349 0.4× 425 1.0× 181 0.5× 38 0.5× 107 1.4× 16 717
William J. Cutter United Kingdom 12 305 0.4× 276 0.7× 212 0.6× 39 0.5× 31 0.4× 16 659
Elizabeth Roof United States 16 889 1.1× 293 0.7× 277 0.7× 49 0.6× 201 2.6× 29 1.0k
Penny Mirrett United States 16 798 1.0× 773 1.9× 260 0.7× 69 0.8× 48 0.6× 19 1.1k
Reymundo Lozano United States 20 819 1.1× 519 1.3× 552 1.4× 35 0.4× 34 0.4× 44 1.1k
Anne Ritvo United States 7 598 0.8× 1.0k 2.5× 185 0.5× 33 0.4× 107 1.4× 7 1.2k
Yujun Shao United States 9 736 0.9× 739 1.8× 313 0.8× 64 0.8× 20 0.3× 18 1.0k
Randi J. Hagerman United States 19 1.4k 1.8× 947 2.3× 852 2.2× 50 0.6× 25 0.3× 31 1.6k

Countries citing papers authored by Martine Borghgraef

Since Specialization
Citations

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

Fields of papers citing papers by Martine Borghgraef

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martine Borghgraef

This figure shows the co-authorship network connecting the top 25 collaborators of Martine Borghgraef. A scholar is included among the top collaborators of Martine Borghgraef 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 Martine Borghgraef. Martine Borghgraef 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.
Garg, Shruti, Ellen Plasschaert, Mie‐Jef Descheemaeker, et al.. (2014). Autism Spectrum Disorder Profile in Neurofibromatosis Type I. Journal of Autism and Developmental Disorders. 45(6). 1649–1657. 53 indexed citations
2.
Eylen, Lien Van, et al.. (2012). Investigating neurocognitive endophenotypes of autism spectrum disorders (ASD) by including an ASD sample with co-occuring neurofibromatosis type 1. Journal of Intellectual Disability Research. 56(10). 927–927. 1 indexed citations
3.
Esch, Hilde Van, Ginevra Zanni, Maureen Holvoet, et al.. (2005). X-linked mental retardation, short stature, microcephaly and hypogonadism maps to Xp22.1-p21.3 in a Belgian family. European Journal of Medical Genetics. 48(2). 145–152. 8 indexed citations
4.
Esch, Hilde Van, René Dom, Martine Borghgraef, et al.. (2004). Screening for FMR-1 premutations in 122 older Flemish males presenting with ataxia. European Journal of Human Genetics. 13(1). 121–123. 47 indexed citations
5.
Steyaert, Jean, Eric Legius, Martine Borghgraef, & J P Fryns. (2002). A distinct neurocognitive phenotype in female fragile‐X premutation carriers assessed with visual attention tasks. American Journal of Medical Genetics Part A. 116A(1). 44–51. 24 indexed citations
6.
Bouras, Nick, David Clarke, Harm Boer, et al.. (1998). Prader–Willi syndrome and psychotic symptoms: I. Case descriptions and genetic studies*. Journal of Intellectual Disability Research. 42(6). 440–450. 31 indexed citations
7.
Chalifoux, Mathieu, P. N. Howard‐Peebles, A Maddalena, et al.. (1997). Natural history of cognitive and adaptive behavior in young fragile X males and females: A 6-year prospective multicenter study. The American Journal of Human Genetics. 61(4).
8.
Borghgraef, Martine, et al.. (1997). Comparison of visual abilities in Williams-Beuren syndrome, Down syndrome and Turner syndrome: A pilot study. 1 indexed citations
9.
Vogels, Annick, et al.. (1996). Trisomy 9p and triploidy: The changing phenotype with age, psychological profile and speech development. 8. 274. 1 indexed citations
10.
Steyaert, Jean, Martine Borghgraef, Eric Legius, & Jean‐Pierre Fryns. (1996). Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 gene. American Journal of Medical Genetics. 64(2). 274–277. 26 indexed citations
11.
Borghgraef, Martine, et al.. (1996). New findings in the behavioral profile of young fraX females. American Journal of Medical Genetics. 64(2). 346–349. 7 indexed citations
12.
Borghgraef, Martine, et al.. (1994). Adults with Williams syndrome: Evaluation of the medical, psychological and behavioural aspects. 229. 2 indexed citations
13.
Engelen, J.J.M., et al.. (1994). Mosaic tetrasomy 8p in two patients: Clinical data and review of the literature. American Journal of Medical Genetics. 50(4). 377–380. 16 indexed citations
14.
Steyaert, Jean, Marleen Decruyenaere, Martine Borghgraef, & Jean‐Pierre Fryns. (1994). Personality profile in adult female fragile X carriers: Assessed with the Minnesota Multiphasic Personality Profile (MMPI). American Journal of Medical Genetics. 51(4). 370–373. 10 indexed citations
15.
Fryns, J. P., et al.. (1993). MCA/MR syndrome with features of Hallermann‐Streiff syndrome and 4q deficiency/ 14q duplication. Clinical Genetics. 44(3). 146–148. 3 indexed citations
16.
Fisch, Gene S., Tadao Arinami, U. Froster‐Iskenius, et al.. (1991). Relationship between age and IQ among fragile X males: A multicenter study. American Journal of Medical Genetics. 38(2-3). 481–487. 24 indexed citations
17.
Curfs, L.M.G., et al.. (1991). Strengths and weaknesses in the cognitive profile of youngsters with Prader‐Willi syndrome. Clinical Genetics. 40(6). 430–434. 70 indexed citations
18.
Borghgraef, Martine, J. P. Fryns, & Herman Van den Berghe. (1990). The female and the fragile X syndrome: data on clinical and psychological findings in 7 fra(X) carriers. Clinical Genetics. 37(5). 341–346. 20 indexed citations
19.
Borghgraef, Martine, et al.. (1988). The 49,XXXXY syndrome. Clinical and psychological follow‐up data. Clinical Genetics. 33(6). 429–434. 21 indexed citations
20.
Borghgraef, Martine, J. P. Fryns, & Herman Van den Berghe. (1988). Psychological findings in three children with ring 15 chromosome. Journal of Intellectual Disability Research. 32(4). 337–347. 6 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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