Anne Gregor

2.2k total citations · 1 hit paper
23 papers, 1.1k citations indexed

About

Anne Gregor is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Anne Gregor has authored 23 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Pulmonary and Respiratory Medicine and 7 papers in Genetics. Recurrent topics in Anne Gregor's work include Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (3 papers) and Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis (3 papers). Anne Gregor is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (3 papers) and Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis (3 papers). Anne Gregor collaborates with scholars based in Germany, United Kingdom and United States. Anne Gregor's co-authors include U. Gatzemeier, Alan B. Sandler, L H Einhorn, Joachim von Pawel, Binh Thanh Nguyen, Claude Denham, Martin Palmer, Clet Niyikiza, John Nemunaitis and C. Manegold and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neuron and Journal of Clinical Oncology.

In The Last Decade

Anne Gregor

20 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.

Phase III Trial of Gemcitabine Plus Cisplatin Versus Cisplatin Alone in Patients With Locally Advanced or Metastatic Non–Small-Cell Lung Cancer

2000 606 citations Alan B. Sandler, John Nemunaitis et al. Journal of Clinical Oncology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anne Gregor Germany	11	541	471	407	201	86	23	1.1k
Vincenzo Di Majo Italy	19	339 0.6×	208 0.4×	562 1.4×	108 0.5×	113 1.3×	49	1.2k
Shiuh‐Wen Luoh United States	21	133 0.2×	538 1.1×	565 1.4×	295 1.5×	148 1.7×	39	1.3k
Thomas Schuetz United States	9	425 0.8×	611 1.3×	279 0.7×	90 0.4×	124 1.4×	17	1.2k
Brendan Horton United States	13	209 0.4×	1.6k 3.3×	484 1.2×	99 0.5×	129 1.5×	52	2.3k
Alexandros Strikoudis United States	13	188 0.3×	184 0.4×	587 1.4×	58 0.3×	68 0.8×	13	887
Maximilian Kauer Austria	20	369 0.7×	237 0.5×	594 1.5×	89 0.4×	251 2.9×	35	1.1k
Yaron Daniely United States	10	141 0.3×	298 0.6×	951 2.3×	154 0.8×	124 1.4×	16	1.3k
Paolo Simi Italy	22	201 0.4×	243 0.5×	633 1.6×	571 2.8×	73 0.8×	82	1.4k
Marielle Ousset Belgium	9	405 0.7×	818 1.7×	821 2.0×	121 0.6×	351 4.1×	12	1.5k
Haim Biran Israel	15	149 0.3×	200 0.4×	260 0.6×	129 0.6×	70 0.8×	40	841

Countries citing papers authored by Anne Gregor

Since Specialization

Citations

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

Fields of papers citing papers by Anne Gregor

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Gregor

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

Gregor, Anne, Niels R. Ntamati, Arif B. Ekici, et al.. (2025). Deregulated ion channels contribute to RHOBTB2-associated developmental and epileptic encephalopathy. Human Molecular Genetics. 34(7). 639–650.

Gregor, Anne, Claudine Rieubland, Matthias Gautschi, et al.. (2025). Heterozygous loss of SRRM1 may be associated with neurodevelopmental phenotypes and anomalies in cell growth and neurite morphology. European Journal of Human Genetics. 34(2). 201–208.

Gregor, Anne, Monika Haubitz, Gabriela M. Baerlocher, et al.. (2025). De Novo Splice‐Site Variant in DKC1 in a Female With Clinical Features of Hoyeraal–Hreidarsson Syndrome. American Journal of Medical Genetics Part A. 197(9). e64097–e64097.

Gregor, Anne, Rodrigo Gutierrez‐Quintana, Jacques Penderis, et al.. (2024). NDUFS7 variant in dogs with Leigh syndrome and its functional validation in a Drosophila melanogaster model. Scientific Reports. 14(1). 2975–2975. 4 indexed citations

Guidugli, Lucia, Monia Hammer, Anne Gregor, et al.. (2023). Novel association of Dandy–Walker malformation with CAPN15 variants expands the phenotype of oculogastrointestinal neurodevelopmental syndrome. American Journal of Medical Genetics Part A. 191(11). 2757–2767. 5 indexed citations

Rapaport, Franck, Bertrand Boisson, Anne Gregor, et al.. (2021). Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance. Proceedings of the National Academy of Sciences. 118(3). 18 indexed citations

Gregor, Anne, et al.. (2020). Genetic interaction screen for severe neurodevelopmental disorders reveals a functional link between Ube3a and Mef2 in Drosophila melanogaster. Scientific Reports. 10(1). 1204–1204. 8 indexed citations

Gregor, Anne, et al.. (2020). Loss of PHF6 leads to aberrant development of human neuron-like cells. Scientific Reports. 10(1). 19030–19030. 3 indexed citations

Li, Hongda, Laura Saucedo-Cuevas, Ling Yuan, et al.. (2019). Zika Virus Protease Cleavage of Host Protein Septin-2 Mediates Mitotic Defects in Neural Progenitors. Neuron. 101(6). 1089–1098.e4. 60 indexed citations

10.

Zaki, Maha S., Amira Masri, Anne Gregor, Joseph G. Gleeson, & Rasim Özgür Rosti. (2015). Dandy–Walker malformation, genitourinary abnormalities, and intellectual disability in two families. American Journal of Medical Genetics Part A. 167(11). 2503–2507. 4 indexed citations

11.

Gregor, Anne, Jamie M. Kramer, Monique van der Voet, et al.. (2014). AlteredGPM6A/M6Dosage Impairs Cognition and Causes Phenotypes Responsive to Cholesterol in Human andDrosophila. Human Mutation. 35(12). 1495–1505. 24 indexed citations

12.

Gregor, Anne, Martin Oti, Evelyn N. Kouwenhoven, et al.. (2013). De Novo Mutations in the Genome Organizer CTCF Cause Intellectual Disability. The American Journal of Human Genetics. 93(1). 124–131. 112 indexed citations

13.

Gregor, Anne, Mandy Krumbiegel, Cornelia Kraus, André Reis, & Christiane Zweier. (2012). De novo triplication of the MAPT gene from the recurrent 17q21.31 microdeletion region in a patient with moderate intellectual disability and various minor anomalies. American Journal of Medical Genetics Part A. 158A(7). 1765–1770. 6 indexed citations

14.

Zweier, Markus, Anne Gregor, Christiane Zweier, et al.. (2010). Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression. Human Mutation. 31(6). 722–733. 114 indexed citations

15.

Putten, John W.G. van, et al.. (2003). A Phase I study of gemcitabine with concurrent radiotherapy in stage III, locally advanced non-small cell lung cancer.. PubMed. 9(7). 2472–7. 44 indexed citations

16.

Sandler, Alan B., John Nemunaitis, Claude Denham, et al.. (2000). Phase III Trial of Gemcitabine Plus Cisplatin Versus Cisplatin Alone in Patients With Locally Advanced or Metastatic Non–Small-Cell Lung Cancer. Journal of Clinical Oncology. 18(1). 122–122. 606 indexed citations breakdown →

17.

McNee, S.G., et al.. (1998). An audit of 3D treatment planning facilities and practice in the UK. Clinical Oncology. 10(1). 18–23. 7 indexed citations

18.

Gregor, Anne, et al.. (1982). Computed tomography in the assessment of malignant mesothelioma of the pleura. Clinical Radiology. 33(1). 67–70. 9 indexed citations

19.

Gregor, Anne, Sushma Singh, M Turner‐Warwick, S. D. Lawler, & W R Parkes. (1979). The role of histocompatibility (HLA) antigens in asbestosis. British Journal of Diseases of the Chest. 73(3). 245–252. 12 indexed citations

20.

Gregor, Anne, Suveer Singh, M Turner‐Warwick, SylviaD. Lawler, & W R Parkes. (1979). The role of histocompatibility (HLA) antigens in asbestosis. British Journal of Diseases of the Chest. 73(3). 245–252. 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.

Explore authors with similar magnitude of impact