Alexandre Bolze

16.6k total citations · 1 hit paper
20 papers, 1.1k citations indexed

About

Alexandre Bolze is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Alexandre Bolze has authored 20 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Molecular Biology and 7 papers in Immunology. Recurrent topics in Alexandre Bolze's work include Genomics and Rare Diseases (6 papers), BRCA gene mutations in cancer (5 papers) and Immunodeficiency and Autoimmune Disorders (4 papers). Alexandre Bolze is often cited by papers focused on Genomics and Rare Diseases (6 papers), BRCA gene mutations in cancer (5 papers) and Immunodeficiency and Autoimmune Disorders (4 papers). Alexandre Bolze collaborates with scholars based in United States, France and United Kingdom. Alexandre Bolze's co-authors include Jean‐Laurent Casanova, Laurent Abel, Aurélie Cobat, Bertrand Boisson, Aziz Belkadi, Yuval Itan, Lei Shang, Quentin B. Vincent, Marissa Teo and Marie Loh and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Experimental Medicine and SHILAP Revista de lepidopterología.

In The Last Decade

Alexandre Bolze

18 papers receiving 1.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants

2015 384 citations Aziz Belkadi, Alexandre Bolze et al. Proceedings of the National Academy of Sciences profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alexandre Bolze United States	10	422	389	364	177	154	20	1.1k
Kazuyoshi Ishigaki Japan	22	431 1.0×	448 1.2×	467 1.3×	121 0.7×	113 0.7×	49	1.3k
Roger Colobrán Spain	20	281 0.7×	552 1.4×	231 0.6×	167 0.9×	58 0.4×	67	1.0k
Daniela Giachino Italy	19	343 0.8×	203 0.5×	740 2.0×	202 1.1×	121 0.8×	51	1.6k
Noor Dawany United States	16	286 0.7×	243 0.6×	286 0.8×	106 0.6×	127 0.8×	28	815
Susan Price United States	18	559 1.3×	606 1.6×	564 1.5×	199 1.1×	48 0.3×	44	1.4k
Britt‐Sabina Petersen Germany	15	328 0.8×	269 0.7×	270 0.7×	70 0.4×	69 0.4×	24	885
Paula Sandrin‐Garcia Brazil	20	128 0.3×	397 1.0×	507 1.4×	99 0.6×	98 0.6×	66	1.1k
Ariel Madrigal United States	9	161 0.4×	626 1.6×	430 1.2×	211 1.2×	82 0.5×	17	1.1k
José Perdomo Australia	16	160 0.4×	365 0.9×	711 2.0×	155 0.9×	78 0.5×	39	1.4k
Anastasios D. Papanastasiou Greece	19	131 0.3×	236 0.6×	315 0.9×	150 0.8×	181 1.2×	62	1.0k

Countries citing papers authored by Alexandre Bolze

Since Specialization

Citations

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

Fields of papers citing papers by Alexandre Bolze

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexandre Bolze

This figure shows the co-authorship network connecting the top 25 collaborators of Alexandre Bolze. A scholar is included among the top collaborators of Alexandre Bolze 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 Alexandre Bolze. Alexandre Bolze 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

Ehlers, Lisa, Selket Delafontaine, Rik Schrijvers, et al.. (2025). Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers. The Journal of Experimental Medicine. 222(11).

Knight, Julian C., et al.. (2025). Human genetics of responses to vaccines. Clinical & Experimental Immunology. 219(1).

Hsieh, Elena W.Y., Alexandre Bolze, & Joseph D. Hernandez. (2024). Inborn errors of immunity illuminate mechanisms of human immunology and pave the road to precision medicine. Immunological Reviews. 322(1). 5–14. 2 indexed citations

Barrett, Kelly M. Schiabor, Natalie Telis, Lisa M. McEwen, et al.. (2024). Underestimated risk of secondary complications in pathogenic and glucose-elevating GCK variant carriers with type 2 diabetes. SHILAP Revista de lepidopterología. 4(1). 239–239. 1 indexed citations

Bolze, Alexandre, Kelly M. Schiabor Barrett, Gai Elhanan, et al.. (2024). Combining rare and common genetic variants improves population risk stratification for breast cancer. SHILAP Revista de lepidopterología. 2. 101826–101826. 5 indexed citations

Cirulli, Elizabeth T., Kelly M. Schiabor Barrett, Alexandre Bolze, et al.. (2024). A power-based sliding window approach to evaluate the clinical impact of rare genetic variants in the nucleotide sequence or the spatial position of the folded protein. Human Genetics and Genomics Advances. 5(3). 100284–100284. 1 indexed citations

Elhanan, Gai, Alexandre Bolze, Iva Neveux, et al.. (2024). Screening Familial Risk for Hereditary Breast and Ovarian Cancer. JAMA Network Open. 7(9). e2435901–e2435901. 2 indexed citations

Barrett, Kelly M. Schiabor, Elizabeth T. Cirulli, Alexandre Bolze, et al.. (2023). Cardiomyopathy prevalence exceeds 30% in individuals with TTN variants and early atrial fibrillation. Genetics in Medicine. 25(4). 100012–100012. 20 indexed citations

Bolze, Alexandre, et al.. (2023). The Potential of Genetics in Identifying Women at Lower Risk of Breast Cancer. JAMA Oncology. 10(2). 236–236. 7 indexed citations

10.

Bolze, Alexandre, Iva Neveux, Kelly M. Schiabor Barrett, et al.. (2022). HLA-A∗03:01 is associated with increased risk of fever, chills, and stronger side effects from Pfizer-BioNTech COVID-19 vaccination. Human Genetics and Genomics Advances. 3(2). 100084–100084. 29 indexed citations

11.

Elhanan, Gai, Iva Neveux, Shaun Dabe, et al.. (2022). Incomplete Penetrance of Population-Based Genetic Screening Results in Electronic Health Record. Frontiers in Genetics. 13. 866169–866169. 6 indexed citations

12.

Barrett, Kelly M. Schiabor, Alexandre Bolze, Yunyun Ni, et al.. (2021). Positive predictive value highlights four novel candidates for actionable genetic screening from analysis of 220,000 clinicogenomic records. Genetics in Medicine. 23(12). 2300–2308. 8 indexed citations

13.

Zhang, Qian, Paul Bastard, Alexandre Bolze, et al.. (2020). Life-Threatening COVID-19: Defective Interferons Unleash Excessive Inflammation. Med. 1(1). 14–20. 77 indexed citations

14.

Meyts, Isabelle, Barbara Bosch, Alexandre Bolze, et al.. (2016). Exome and genome sequencing for inborn errors of immunity. Journal of Allergy and Clinical Immunology. 138(4). 957–969. 124 indexed citations

15.

Belkadi, Aziz, Alexandre Bolze, Yuval Itan, et al.. (2015). Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants. Proceedings of the National Academy of Sciences. 112(17). 5473–5478. 384 indexed citations breakdown →

16.

Bolze, Alexandre, Avinash Abhyankar, Audrey V. Grant, et al.. (2012). A Mild Form of SLC29A3 Disorder: A Frameshift Deletion Leads to the Paradoxical Translation of an Otherwise Noncoding mRNA Splice Variant. PLoS ONE. 7(1). e29708–e29708. 44 indexed citations

17.

Koss, Matthew, Alexandre Bolze, Andrea Brendolan, et al.. (2012). Congenital Asplenia in Mice and Humans with Mutations in a Pbx/Nkx2-5/p15 Module. Developmental Cell. 22(5). 913–926. 52 indexed citations

18.

Bolze, Alexandre, Minji Byun, David McDonald, et al.. (2010). Whole-Exome-Sequencing-Based Discovery of Human FADD Deficiency. The American Journal of Human Genetics. 87(6). 873–881. 118 indexed citations

19.

Mahlaoui, Nizar, Véronique Minard‐Colin, Capucine Pïcard, et al.. (2010). Isolated Congenital Asplenia: A French Nationwide Retrospective Survey of 20 Cases. The Journal of Pediatrics. 158(1). 142–148.e1. 36 indexed citations

20.

Chew, Valerie, Charlene Tow, Marissa Teo, et al.. (2009). Inflammatory tumour microenvironment is associated with superior survival in hepatocellular carcinoma patients. Journal of Hepatology. 52(3). 370–379. 214 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.

Explore authors with similar magnitude of impact