Alban Ziegler

2.0k total citations
29 papers, 518 citations indexed

About

Alban Ziegler is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Alban Ziegler has authored 29 papers receiving a total of 518 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 15 papers in Genetics and 4 papers in Clinical Biochemistry. Recurrent topics in Alban Ziegler's work include Genomics and Rare Diseases (10 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomic variations and chromosomal abnormalities (5 papers). Alban Ziegler is often cited by papers focused on Genomics and Rare Diseases (10 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomic variations and chromosomal abnormalities (5 papers). Alban Ziegler collaborates with scholars based in France, United States and Germany. Alban Ziegler's co-authors include Benjamin K. Pannell, Li Zuo, Tingyang Zhou, Thomas M. Best, Dominique Bonneau, Estelle Colin, Wendy K. Chung, David Goudenège, Siddharth Banka and Myung Hee Park and has published in prestigious journals such as JAMA, Nature Medicine and Molecular and Cellular Biology.

In The Last Decade

Alban Ziegler

25 papers receiving 513 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alban Ziegler France 9 252 81 75 39 35 29 518
Antonella La Russa Italy 17 251 1.0× 79 1.0× 119 1.6× 76 1.9× 32 0.9× 46 817
Junsuke Uwada Japan 19 449 1.8× 80 1.0× 125 1.7× 43 1.1× 45 1.3× 47 751
Yongan Wang China 16 228 0.9× 45 0.6× 36 0.5× 56 1.4× 29 0.8× 50 654
Min Cui China 15 265 1.1× 97 1.2× 34 0.5× 32 0.8× 25 0.7× 31 619
Blanka Holendová Czechia 15 374 1.5× 69 0.9× 176 2.3× 34 0.9× 50 1.4× 29 676
Mohammad Ali Takhshid Iran 14 236 0.9× 44 0.5× 114 1.5× 25 0.6× 15 0.4× 59 604
Isabelle Doignon France 15 236 0.9× 33 0.4× 47 0.6× 40 1.0× 28 0.8× 23 809
Maie Al‐Bader Kuwait 16 290 1.2× 154 1.9× 36 0.5× 59 1.5× 22 0.6× 41 797
Kristina Cusmano‐Ozog United States 14 448 1.8× 125 1.5× 87 1.2× 31 0.8× 37 1.1× 37 774
Atsushi Masuda Japan 13 285 1.1× 35 0.4× 49 0.7× 41 1.1× 28 0.8× 39 678

Countries citing papers authored by Alban Ziegler

Since Specialization
Citations

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

Fields of papers citing papers by Alban Ziegler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alban Ziegler

This figure shows the co-authorship network connecting the top 25 collaborators of Alban Ziegler. A scholar is included among the top collaborators of Alban Ziegler 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 Alban Ziegler. Alban Ziegler 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.
Ziegler, Alban & Wendy K. Chung. (2025). Genomic newborn screening: exploring opportunities and navigating pitfalls while ensuring inclusivity. Trends in Genetics. 41(8). 631–634.
2.
Ziegler, Alban & Wendy K. Chung. (2025). Newborn Screening Using Genome Sequencing for Early Actionable Conditions—Reply. JAMA. 333(12). 1088–1088. 2 indexed citations
3.
Ziegler, Alban, Joanne Carroll, Jennifer Bain, et al.. (2024). Antisense oligonucleotide therapy in an individual with KIF1A-associated neurological disorder. Nature Medicine. 30(10). 2782–2786. 14 indexed citations
4.
Snelling, Tom, Isabelle Jéru, Laurence Cuisset, et al.. (2024). Discovery and functional analysis of a novel ALPK1 variant in ROSAH syndrome. Open Biology. 14(12). 240260–240260. 6 indexed citations
5.
Buffet, Alexandre, Alexandra Bruel, Rodolphe Dard, et al.. (2024). X-linked transient antenatal Bartter syndrome related to MAGED2 gene: Enriching the phenotypic description and pathophysiologic investigation. Genetics in Medicine. 27(2). 101217–101217. 1 indexed citations
6.
Takatsu, Hiroyuki, Yusuke Kosugi, Haruo Ogawa, et al.. (2024). De Novo Missense Variations of ATP8B2 Impair Its Phosphatidylcholine Flippase Activity. Molecular and Cellular Biology. 44(11). 473–488. 1 indexed citations
7.
Ziegler, Alban, Ruben Meyer, Dominique Bonneau, et al.. (2024). Heterozygous gain of function variant in GUCY1A2 may cause autonomous ovarian hyperfunction. European Journal of Endocrinology. 190(4). 266–274. 1 indexed citations
8.
9.
Chussid, Steven, et al.. (2023). Caregiver‐reported dental manifestations in individuals with genetic neurodevelopmental disorders. International Journal of Paediatric Dentistry. 34(2). 145–152.
10.
Huang, Liping, Catherine P. Kirschke, Marie‐Christine Copin, et al.. (2023). Identification of novel compound heterozygous variants in the SLC30A7 (ZNT7) gene in two French brothers with stunted growth, testicular hypoplasia and bone marrow failure. Human Molecular Genetics. 32(12). 2016–2031. 5 indexed citations
11.
Schönewolf‐Greulich, Bitten, Alexandra Afenjar, Magalie Barth, et al.. (2021). Clinical and molecular delineation of PUS3 ‐associated neurodevelopmental disorders. Clinical Genetics. 100(5). 628–633. 26 indexed citations
12.
Alsaif, Hessa S., Eissa Faqeih, Magalie Barth, et al.. (2021). ZNF668 deficiency causes a recognizable disorder of DNA damage repair. Human Genetics. 140(9). 1395–1401. 1 indexed citations
13.
Park, Myung Hee, et al.. (2021). Post-translational formation of hypusine in eIF5A: implications in human neurodevelopment. Amino Acids. 54(4). 485–499. 25 indexed citations
14.
Serranová, Tereza, Estelle Colin, Alban Ziegler, et al.. (2021). Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variant. Neurogenetics. 22(2). 137–141. 3 indexed citations
15.
Harms, Frederike L., Malik Alawi, Sigrid Fuchs, et al.. (2020). Biallelic loss‐of‐function variants in TBC1D2B cause a neurodevelopmental disorder with seizures and gingival overgrowth. Human Mutation. 41(9). 1645–1661. 13 indexed citations
16.
Ziegler, Alban, Patricia I. Bader, Kirsty McWalter, et al.. (2019). Confirmation that variants in TTI2 are responsible for autosomal recessive intellectual disability. Clinical Genetics. 96(4). 354–358. 8 indexed citations
17.
Boussion, F., Stéphane Triau, Majida Charif, et al.. (2019). Second report of RING finger protein 113A (RNF113A) involvement in a Mendelian disorder. American Journal of Medical Genetics Part A. 182(3). 565–569. 7 indexed citations
18.
Zuo, Li, Tingyang Zhou, Benjamin K. Pannell, Alban Ziegler, & Thomas M. Best. (2015). Biological and physiological role of reactive oxygen species - the good, the bad and the ugly. Acta Physiologica. 214(3). 329–348. 333 indexed citations
19.
Colin, Estelle, F. Boussion, Philippe Latour, et al.. (2015). In Utero Diagnosis of Niemann–Pick Type C in the Absence of Family History. JIMD Reports. 28. 105–110. 6 indexed citations
20.
Ziegler, Alban, Agnès Guichet, Magalie Barth, et al.. (2014). Extensive Mongolian spots in 4p16.3 deletion (Wolf–Hirschhorn syndrome). Clinical Dysmorphology. 23(3). 109–110. 1 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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