Bernard Conrad

3.5k total citations
24 papers, 1.8k citations indexed

About

Bernard Conrad is a scholar working on Genetics, Immunology and Molecular Biology. According to data from OpenAlex, Bernard Conrad has authored 24 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Immunology and 6 papers in Molecular Biology. Recurrent topics in Bernard Conrad's work include Genomic variations and chromosomal abnormalities (7 papers), T-cell and B-cell Immunology (7 papers) and Genomics and Rare Diseases (4 papers). Bernard Conrad is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), T-cell and B-cell Immunology (7 papers) and Genomics and Rare Diseases (4 papers). Bernard Conrad collaborates with scholars based in Switzerland, United States and France. Bernard Conrad's co-authors include Stylianos E. Antonarakis, Bernard Mach, Brigitte T. Huber, Natalie Sutkowski, Jörg Schüpbach, Jürg Böni, Samuel Marguerat, R. Behboo, David N. Finegold and Camillo Ricordi and has published in prestigious journals such as Nature, Cell and Nature Genetics.

In The Last Decade

Bernard Conrad

23 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bernard Conrad Switzerland 15 668 657 556 368 196 24 1.8k
L. Gebuhrer France 24 933 1.4× 294 0.4× 250 0.4× 151 0.4× 180 0.9× 92 1.8k
Jean-Luc Blond France 8 403 0.6× 1.0k 1.5× 341 0.6× 745 2.0× 68 0.3× 9 1.8k
Shawn L. Chavez United States 24 806 1.2× 1.5k 2.3× 335 0.6× 353 1.0× 182 0.9× 44 3.0k
Jennifer M. Love New Zealand 11 290 0.4× 591 0.9× 789 1.4× 131 0.4× 222 1.1× 28 1.3k
Sarah Field United Kingdom 13 660 1.0× 584 0.9× 664 1.2× 46 0.1× 278 1.4× 20 1.8k
Hayato Kotaki Japan 9 1.1k 1.6× 570 0.9× 145 0.3× 126 0.3× 108 0.6× 11 2.1k
Esther Caparrós Spain 20 663 1.0× 1.1k 1.6× 182 0.3× 72 0.2× 146 0.7× 34 2.4k
Alisoun H. Carey United Kingdom 18 437 0.7× 1.2k 1.9× 926 1.7× 66 0.2× 226 1.2× 26 2.2k
Iris H. Jonkers Netherlands 21 223 0.3× 2.1k 3.3× 673 1.2× 174 0.5× 103 0.5× 41 2.7k
Christophe Viret France 26 1.7k 2.5× 518 0.8× 201 0.4× 128 0.3× 62 0.3× 66 2.5k

Countries citing papers authored by Bernard Conrad

Since Specialization
Citations

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

Fields of papers citing papers by Bernard Conrad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernard Conrad

This figure shows the co-authorship network connecting the top 25 collaborators of Bernard Conrad. A scholar is included among the top collaborators of Bernard Conrad 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 Bernard Conrad. Bernard Conrad 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.
2.
Major, Attila, et al.. (2019). Rare case of remission of a patient with small cell carcinoma of the ovary, hypercalcaemic type (SCCOHT) stage IV: Case report. International Journal of Surgery Case Reports. 66. 398–403. 5 indexed citations
3.
Pescia, G, Nicolas Guex, Christian Iseli, et al.. (2016). Cell-free DNA testing of an extended range of chromosomal anomalies: clinical experience with 6,388 consecutive cases. Genetics in Medicine. 19(2). 169–175. 73 indexed citations
4.
Goeggel‐Simonetti, Barbara, Maja Steinlin, Roland Wiest, et al.. (2011). Contiguous ∼16 Mb 1p36 deletion: Dominant features of classical distal 1p36 monosomy with haplo‐lethality. American Journal of Medical Genetics Part A. 155(8). 1964–1968. 10 indexed citations
5.
Strozzi, Susi, Roland Kreis, Franziska Joncourt, et al.. (2010). Neuropsychological impairments and the impact of dystrophin mutations on general cognitive functioning of patients with Duchenne muscular dystrophy. Journal of Clinical Neuroscience. 18(1). 90–95. 57 indexed citations
6.
Béna, Frédérique, et al.. (2007). A de novo 1.1–1.6 Mb subtelomeric deletion of chromosome 20q13.33 in a patient with learning difficulties but without obvious dysmorphic features. American Journal of Medical Genetics Part A. 143A(16). 1894–1899. 13 indexed citations
7.
Conrad, Bernard & Stylianos E. Antonarakis. (2007). Gene Duplication: A Drive for Phenotypic Diversity and Cause of Human Disease. Annual Review of Genomics and Human Genetics. 8(1). 17–35. 194 indexed citations
8.
Bottani, Armand, Alfredo Orrico, Lucia Galli, et al.. (2007). Unilateral focal polymicrogyria in a patient with classical Aarskog–Scott syndrome due to a novel missense mutation in an evolutionary conserved RhoGEF domain of the faciogenital dysplasia gene FGD1. American Journal of Medical Genetics Part A. 143A(19). 2334–2338. 19 indexed citations
9.
Bottani, Armand, Jamel Chelly, Arjan P.M. de Brouwer, et al.. (2007). Sequence variation in ultraconserved and highly conserved elements does not cause X‐linked mental retardation. American Journal of Medical Genetics Part A. 143A(8). 888–890. 3 indexed citations
10.
Meylan, Françoise, Magda De Smedt, Georges Leclercq, et al.. (2005). Negative thymocyte selection to HERV-K18 superantigens in humans. Blood. 105(11). 4377–4382. 26 indexed citations
11.
Leupin, Olivier, Catia Attanasio, Samuel Marguerat, et al.. (2005). Transcriptional activation by bidirectional RNA polymerase II elongation over a silent promoter. EMBO Reports. 6(10). 956–960. 11 indexed citations
12.
13.
Marguerat, Samuel, Françoise Meylan, Catherine Ucla, et al.. (2001). Interferon-α-Induced Endogenous Superantigen. Immunity. 15(4). 591–601. 115 indexed citations
14.
Sutkowski, Natalie, et al.. (2001). Epstein-Barr Virus Transactivates the Human Endogenous Retrovirus HERV-K18 that Encodes a Superantigen. Immunity. 15(4). 579–589. 243 indexed citations
15.
Conrad, Bernard. (1998). In Response to Murphy et al., Löwer et al., and Lan et al. Cell. 95(1). 16–16. 6 indexed citations
16.
Masternak, Krzysztof, Emmanuèle Barras, Madeleine Zufferey, et al.. (1998). A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients. Nature Genetics. 20(3). 273–277. 232 indexed citations
17.
Conrad, Bernard, et al.. (1997). A Human Endogenous Retroviral Superantigen as Candidate Autoimmune Gene in Type I Diabetes. Cell. 90(2). 303–313. 327 indexed citations
18.
Conrad, Bernard & Massimo Trucco. (1994). Superantigens as etiopathogenetic factors in the development of insulin‐dependent diabetes mellitus. Diabetes/Metabolism Reviews. 10(4). 309–338. 16 indexed citations
19.
Conrad, Bernard, Eckhart Weidmann, Giuliana Trucco, et al.. (1994). Evidence for superantigen involvement in insulin-dependent diabetes mellitus aetiology. Nature. 371(6495). 351–355. 258 indexed citations
20.
Wren, Sherry M., Stewart C. Wang, Ngoc Thai, et al.. (1993). EVIDENCE FOR EARLY Th 2 T CELL PREDOMINANCE IN XENOREACTIVITY. Transplantation. 56(4). 905–910. 36 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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