Pierre Lindenbaum

2.6k total citations
23 papers, 723 citations indexed

About

Pierre Lindenbaum is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Pierre Lindenbaum has authored 23 papers receiving a total of 723 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Pierre Lindenbaum's work include Genomics and Phylogenetic Studies (5 papers), Virus-based gene therapy research (4 papers) and Viral Infectious Diseases and Gene Expression in Insects (3 papers). Pierre Lindenbaum is often cited by papers focused on Genomics and Phylogenetic Studies (5 papers), Virus-based gene therapy research (4 papers) and Viral Infectious Diseases and Gene Expression in Insects (3 papers). Pierre Lindenbaum collaborates with scholars based in France, United States and United Kingdom. Pierre Lindenbaum's co-authors include Richard Redon, Didier Poncet, R. L’Haridon, J. Cohen, Olivier Pichon, Cédric Le Caignec, Christian Dina, Laurence Faivre, Albert David and Sébastien Jacquemont and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Bioinformatics.

In The Last Decade

Pierre Lindenbaum

23 papers receiving 707 citations

Peers

Pierre Lindenbaum
Simon Pacouret United States
Eric Zinn United States
Adam D. Ewing Australia
Ryan L. Collins United States
Thomas B. Lentz United States
Samantha Cooper United States
Xueqiu Lin United States
Simon Pacouret United States
Pierre Lindenbaum
Citations per year, relative to Pierre Lindenbaum Pierre Lindenbaum (= 1×) peers Simon Pacouret

Countries citing papers authored by Pierre Lindenbaum

Since Specialization
Citations

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

Fields of papers citing papers by Pierre Lindenbaum

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pierre Lindenbaum

This figure shows the co-authorship network connecting the top 25 collaborators of Pierre Lindenbaum. A scholar is included among the top collaborators of Pierre Lindenbaum 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 Pierre Lindenbaum. Pierre Lindenbaum 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.
Forest, Virginie, Pierre Lindenbaum, Estelle Baron, et al.. (2024). Generation of a patient-specific induced pluripotent stem cell line carrying the DES p.R406W mutation, an isogenic control and a DES p.R406W knock-in line. Stem Cell Research. 77. 103396–103396. 1 indexed citations
2.
Hervé, Julie, Karine Haurogné, Marie Allard, et al.. (2024). Spontaneous Akt2 deficiency in a colony of NOD mice exhibiting early diabetes. Scientific Reports. 14(1). 9100–9100. 1 indexed citations
3.
Janin, Alexandre, Amandine Caillaud, Antoine Rimbert, et al.. (2022). APOB CRISPR-Cas9 Engineering in Hypobetalipoproteinemia: A Promising Tool for Functional Studies of Novel Variants. International Journal of Molecular Sciences. 23(8). 4281–4281. 7 indexed citations
4.
Caignec, Cédric Le, Olivier Pichon, C. Bonnard, et al.. (2019). Fryns type mesomelic dysplasia of the upper limbs caused by inverted duplications of the HOXD gene cluster. European Journal of Human Genetics. 28(3). 324–332. 10 indexed citations
5.
Penaud‐Budloo, Magalie, Sylvie Saleün, Alain Roulet, et al.. (2017). Accurate Identification and Quantification of DNA Species by Next-Generation Sequencing in Adeno-Associated Viral Vectors Produced in Insect Cells. Human Gene Therapy Methods. 28(3). 148–162. 37 indexed citations
6.
Cogné, Benjamin, Pierre Lindenbaum, Matthias Hebben, et al.. (2015). Advanced Characterization of DNA Molecules in rAAV Vector Preparations by Single-stranded Virus Next-generation Sequencing. Molecular Therapy — Nucleic Acids. 4. e260–e260. 62 indexed citations
7.
Georger, Christophe, Béatrice Marolleau, Laurence Jeanson-Leh, et al.. (2015). Short-lived recombinant adeno-associated virus transgene expression in dystrophic muscle is associated with oxidative damage to transgene mRNA. Molecular Therapy — Methods & Clinical Development. 2. 15010–15010. 14 indexed citations
8.
Charpentier, Éric, Pierre Lindenbaum, Olivier Pichon, et al.. (2015). Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients With Coarctation of the Aorta. Circulation Cardiovascular Genetics. 9(1). 86–94. 29 indexed citations
9.
Lindenbaum, Pierre & Richard Redon. (2014). mod_bio: Apache modules for Next-Generation sequencing data. Bioinformatics. 31(1). 112–113. 1 indexed citations
10.
Marionneau, Céline, Cheryl F. Lichti, Pierre Lindenbaum, et al.. (2012). Mass Spectrometry-Based Identification of Native Cardiac Nav1.5 Channel α Subunit Phosphorylation Sites. Journal of Proteome Research. 11(12). 5994–6007. 39 indexed citations
11.
Isidor, Bertrand, Pierre Lindenbaum, Olivier Pichon, et al.. (2011). Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis. Nature Genetics. 43(4). 306–308. 148 indexed citations
12.
Parnell, Laurence D., Pierre Lindenbaum, Khader Shameer, et al.. (2011). BioStar: An Online Question & Answer Resource for the Bioinformatics Community. PLoS Computational Biology. 7(10). e1002216–e1002216. 66 indexed citations
13.
Lindenbaum, Pierre. (2010). Publishers’ Booklists in Late Seventeenth-Century London. The Library. 11(4). 381–404. 4 indexed citations
14.
Lindenbaum, Pierre, et al.. (2009). The Gene Wiki: community intelligence applied to human gene annotation. Nucleic Acids Research. 38(suppl_1). D633–D639. 58 indexed citations
15.
Brooks, Peter, Charles Marcaillou, Jean‐Paul Saraiva, et al.. (2009). Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta. BMC Genetics. 10(1). 16–16. 6 indexed citations
16.
Philippi, Anne, Frédéric Torès, Jérôme Carayol, et al.. (2007). Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis. BMC Medical Genetics. 8(1). 74–74. 30 indexed citations
17.
Philippi, Anne, Frédéric Torès, Pierre Lindenbaum, et al.. (2005). Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism. Molecular Psychiatry. 10(10). 950–960. 53 indexed citations
18.
Lindenbaum, Pierre. (2002). Authors and Publishers in the Late Seventeenth Century, II: Brabazon Aylmer and the Mysteries of the Trade. The Library. 3(1). 32–57. 5 indexed citations
19.
Lindenbaum, Pierre. (1998). CloneIt: finding cloning strategies, in-frame deletions and frameshifts.. Bioinformatics. 14(5). 465–466. 3 indexed citations
20.
Poncet, Didier, Pierre Lindenbaum, R. L’Haridon, & J. Cohen. (1997). In vivo and in vitro phosphorylation of rotavirus NSP5 correlates with its localization in viroplasms. Journal of Virology. 71(1). 34–41. 79 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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