B Quack

711 total citations
23 papers, 513 citations indexed

About

B Quack is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, B Quack has authored 23 papers receiving a total of 513 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 13 papers in Molecular Biology and 6 papers in Plant Science. Recurrent topics in B Quack's work include Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). B Quack is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). B Quack collaborates with scholars based in France, United States and United Kingdom. B Quack's co-authors include B Noël, J. M. Luciani, R.M. Speed, Jacqueline Levilliers, Christine Petit, J. Weissenbach, I Emerit, A. C. Chandley, Marie-Roberte Guichaoua and Benjamin Noël and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

B Quack

23 papers receiving 432 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
B Quack France	13	396	250	195	128	57	23	513
Roberto Coco Argentina	12	401 1.0×	213 0.9×	143 0.7×	156 1.2×	131 2.3×	45	531
I. H. Pawlowitzki Germany	14	239 0.6×	286 1.1×	114 0.6×	99 0.8×	50 0.9×	45	528
H. F. de France Netherlands	13	324 0.8×	144 0.6×	129 0.7×	180 1.4×	89 1.6×	24	459
Jacques Puechberty France	17	458 1.2×	355 1.4×	311 1.6×	221 1.7×	29 0.5×	43	729
Geneviève Lefort France	13	262 0.7×	148 0.6×	105 0.5×	160 1.3×	22 0.4×	29	375
Claudine Fear United Kingdom	10	229 0.6×	147 0.6×	36 0.2×	74 0.6×	12 0.2×	16	312
M. G. Daker United Kingdom	13	333 0.8×	225 0.9×	113 0.6×	82 0.6×	47 0.8×	28	538
Anna Frackiewicz United Kingdom	9	390 1.0×	200 0.8×	209 1.1×	185 1.4×	91 1.6×	9	532
Joleen L. Zackowski United States	11	311 0.8×	151 0.6×	105 0.5×	107 0.8×	23 0.4×	13	379
Marjorie Newton United Kingdom	7	280 0.7×	179 0.7×	113 0.6×	81 0.6×	71 1.2×	9	409

Countries citing papers authored by B Quack

Since Specialization

Citations

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

Fields of papers citing papers by B Quack

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B Quack

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Lesca, Gaëtan, et al.. (2003). Clinical, cytogenetic, and molecular description of a FRAXE French family. Psychiatric Genetics. 13(1). 43–46. 3 indexed citations

Verschraegen-Spae, M.R., B Quack, Sophie Rousseaux, et al.. (1998). Application of fluorescence in situ hybridization to the identification of different marker chromosomes.. PubMed. 41(1). 5–10. 1 indexed citations

Quack, B, Nadine Van Roy, M.R. Verschraegen-Spae, & Franz Klein. (1992). Interstitial deletion and ring chromosome derived from 19q. Proximal 19q trisomy phenotype.. PubMed. 35(4). 241–4. 22 indexed citations

Guichaoua, Marie-Roberte, B Quack, R.M. Speed, et al.. (1990). Infertility in human males with autosomal translocations: meiotic study of a 14;22 Robertsonian translocation. Human Genetics. 86(2). 162–6. 66 indexed citations

Lavedan, Christian, F. Barichard, P. Couillin, et al.. (1989). Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13. Cytogenetic and Genome Research. 50(2-3). 70–74. 27 indexed citations

Quack, B, Patrick M. Guérin, J Ruffié, & G Lucotte. (1988). Mapping of probe p49f to the proximal part of the human Y chromosome long arm. Cytogenetic and Genome Research. 47(4). 232–232. 24 indexed citations

Quack, B, R.M. Speed, J. M. Luciani, et al.. (1988). Meiotic analysis of two human reciprocal X-autosome translocations. Cytogenetic and Genome Research. 48(1). 43–47. 48 indexed citations

Quack, B, Benjamin Noël, & Alaín Le Moine. (1987). Chromosome 18 variant with increased centromeric tandemly repeated DNA in a family.. PubMed. 30(2). 85–90. 5 indexed citations

Quack, B, et al.. (1978). [Constitutional stereotyped gap in human chromosomes (author's transl)].. PubMed. 26(1). 55–67. 4 indexed citations

10.

Noël, Benjamin, et al.. (1977). Selective endoreduplication or branched chromosome?. Experimental Cell Research. 104(2). 423–426. 15 indexed citations

11.

Quack, B & B Noël. (1977). The XY chromosome pair in mouse and human spermatocytes, visualised by silver staining. Nature. 267(5610). 431–433. 31 indexed citations

12.

Nielsen, Johannes, et al.. (1974). BRILLIANTLY FLUORESCING ENLARGED SHORT ARMS D OR G. The Lancet. 303(7865). 1049–1050. 17 indexed citations

13.

Quack, B, et al.. (1974). The XYY Syndrome: Reality or Myth?. Clinical Genetics. 5(5). 387–394. 24 indexed citations

14.

Noël, B, et al.. (1974). [Identification of 47, XYY men in the general population using fluorescence staining of heterochromatin].. PubMed. 22(1). 31–43. 2 indexed citations

15.

Noël, B, et al.. (1973). [Identification of the small submetacentric supernumerary chromosome in the cat's-eye syndrome].. PubMed. 21(1). 23–32. 2 indexed citations

16.

Emerit, I, et al.. (1972). Short arm deletion of chromosome 14. Human Genetics. 15(1). 33–38. 4 indexed citations

17.

Noël, B, I Emerit, J. M. Luciani, & B Quack. (1971). A familial Y/autosome translocation in man. Clinical Genetics. 2(1). 1–6. 48 indexed citations

18.

Noël, B, et al.. (1969). Peroxydases leucocytaires et caryotype 47, XYY.. Annales de Génétique. 12(1). 2 indexed citations

19.

Noël, B, et al.. (1968). [Male pseudohermaphroditism and mosaicism 45,X-46,XYdic-46,XXq-].. PubMed. 11(1). 62–5. 6 indexed citations

20.

Noël, Benjamin, B Quack, & Marc Thiriet. (1968). [Segregation of a balanced translocation t(5p-;Gp+)].. PubMed. 11(4). 247–52. 12 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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