N. Créau-Goldberg

874 total citations
29 papers, 581 citations indexed

About

N. Créau-Goldberg is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, N. Créau-Goldberg has authored 29 papers receiving a total of 581 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Plant Science. Recurrent topics in N. Créau-Goldberg's work include Chromosomal and Genetic Variations (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic Mapping and Diversity in Plants and Animals (3 papers). N. Créau-Goldberg is often cited by papers focused on Chromosomal and Genetic Variations (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic Mapping and Diversity in Plants and Animals (3 papers). N. Créau-Goldberg collaborates with scholars based in France, Netherlands and Canada. N. Créau-Goldberg's co-authors include C Turleau, J. de Grouchy, Annie Nicole, Alain Aurias, Zohra Rahmani, M Poissonnier, Jean‐Louis Blouin, Paul C. Watkins, Zoubida Chettouh and J. F. Mattéi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Immunology and British Journal of Cancer.

In The Last Decade

N. Créau-Goldberg

29 papers receiving 569 citations

Peers

N. Créau-Goldberg

GENET

PHEOH

PPCH

Claude‐Lise Richer Canada

Cathy M. Tuck‐Müller United States

Ai Shintani Japan

Karen Fancher United States

Maxine J. Sutcliffe United States

M. S. NEWTON United Kingdom

Daniela Balzereit Germany

Betty Féret France

Tomohiko Akiyama Japan

Linda Meredith United Kingdom

Claude‐Lise Richer Canada

N. Créau-Goldberg

458 ×1.4

397 ×1.3

GENET

56 ×0.3

PHEOH

194 ×1.9

95 ×1.2

PPCH

Citations per year, relative to N. Créau-Goldberg N. Créau-Goldberg (= 1×) peers Claude‐Lise Richer

Countries citing papers authored by N. Créau-Goldberg

Since Specialization

Citations

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

Fields of papers citing papers by N. Créau-Goldberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by N. Créau-Goldberg. 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 N. Créau-Goldberg. The network helps show where N. Créau-Goldberg may publish in the future.

Co-authorship network of co-authors of N. Créau-Goldberg

This figure shows the co-authorship network connecting the top 25 collaborators of N. Créau-Goldberg. A scholar is included among the top collaborators of N. Créau-Goldberg 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 N. Créau-Goldberg. N. Créau-Goldberg 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

Rahmani, Zohra, Jean‐Louis Blouin, N. Créau-Goldberg, et al.. (2005). Down syndrome critical region around D21S55 on proximal 21q22.3. American Journal of Medical Genetics. 37(S7). 98–103. 27 indexed citations

Gosset, Philippe, Didier Theophile, Martine Duterque‐Coquillaud, et al.. (1993). Mapping the Down Syndrome Chromosome Region. European Journal of Human Genetics. 1(1). 51–63. 24 indexed citations

Plougastel-Douglas, Béatrice, P. Couillin, Véronique Blanquet, et al.. (1992). Mapping around the Xq13.1 breakpoints of two X/A translocations in hypohidrotic ectodermal dysplasia (EDA) female patients. Genomics. 14(2). 523–525. 7 indexed citations

Yaspo, Marie‐Laure, Didier Theophile, Alain Aurias, et al.. (1992). Molecular analysis of 12 patients with the t(8;2l) translocation and M2 acute myelogenous leukemia. Genes Chromosomes and Cancer. 5(2). 166–177. 5 indexed citations

Blanquet, Véronique, C Turleau, J. de Grouchy, & N. Créau-Goldberg. (1991). Physical map around the retinoblastoma gene: Possible genomic imprinting suggested by NruI digestion. Genomics. 10(2). 350–355. 13 indexed citations

Blanquet, Véronique, N. Créau-Goldberg, J. de Grouchy, & C Turleau. (1991). Molecular detection of constitutional deletions in patients with retinoblastoma. American Journal of Medical Genetics. 39(3). 355–361. 14 indexed citations

Grouchy, J. de, Annie Nicole, Claude Cochet, Pierre‐Marie Sinet, & N. Créau-Goldberg. (1991). Increased SOD1 enzymatic activity and gene modifications in orangutans: evolutionary implications. Human Genetics. 87(5). 567–570. 1 indexed citations

Rahmani, Zohra, Jean‐Louis Blouin, N. Créau-Goldberg, et al.. (1989). Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.. Proceedings of the National Academy of Sciences. 86(15). 5958–5962. 209 indexed citations

Delattre, Olivier, Anne Bernard, Bernard Malfoy, et al.. (1988). Studies on the Human Chromosome 3 Centromere with a Newly Cloned Alphoid DNA Probe. Human Heredity. 38(3). 156–167. 14 indexed citations

10.

Goldgaber, D, C Turleau, N. Créau-Goldberg, et al.. (1987). The beta amyloid protein (AD-AP) cDNA hybridizes in normal and Alzheimer individuals near the interface of 21q21 and q22.1.. PubMed. 30(2). 68–9. 23 indexed citations

11.

Lalley, P.A., Stephen J. O’Brien, N. Créau-Goldberg, et al.. (1987). Report of the committee on comparative mapping. Cytogenetic and Genome Research. 46(1-4). 367–389. 23 indexed citations

12.

Créau-Goldberg, N., Anne Gégonne, Jean Maurice Delabar, et al.. (1987). Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphism. Human Genetics. 76(4). 396–398. 47 indexed citations

13.

Jeanpierre, Marc, Dominique Weil, P. Gallano, N. Créau-Goldberg, & Claudine Junien. (1985). The organization of two related subfamilies of a human tandemly repeated DNA is chromosome specific. Human Genetics. 70(4). 302–310. 18 indexed citations

14.

Créau-Goldberg, N., et al.. (1984). Conservation of the human COL1A1-TK-GAA synteny and homoeologous assignment in the African green monkey and the baboon (Cercopithecoidae). Human Genetics. 68(4). 333–336. 3 indexed citations

15.

Davisson, Muriel T., et al.. (1984). Report of the committee on comparative mapping. Cytogenetic and Genome Research. 37(1-4). 312–339. 31 indexed citations

16.

Créau-Goldberg, N., C Turleau, Claude Cochet, & de Grouchy J. (1983). New gene assignments in the baboon and new chromosome homoeologies with man.. PubMed. 26(2). 75–8. 6 indexed citations

17.

Robbins, Lynn W., L. Gayle Littlefield, Shirley P. Colyer, et al.. (1981). Human cytogenetic nomenclature. Cytogenetic and Genome Research. 31(4). 193–193. 1 indexed citations

18.

Créau-Goldberg, N., Claude Cochet, C Turleau, C. Finaz, & J. de Grouchy. (1980). Comparative gene mapping of man and <i>Cebus capucinus</i> for PGD, ENO1, PGM1, PGM2, and SOD1. Cytogenetic and Genome Research. 28(1-2). 140–142. 6 indexed citations

19.

Créau-Goldberg, N. & J C Salomon. (1980). Immunotherapy of primary methylcholanthrene-induced mouse tumours by intratumoral BCG. British Journal of Cancer. 41(4). 541–552. 5 indexed citations

20.

Pillot, J, et al.. (1976). Lack of Antibody Activity Directed against the Most Common Human Bacteria in Human Myeloma Protein. The Journal of Immunology. 117(5_Part_2). 2042–2044. 3 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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