Jacqueline Maciazek

5.8k total citations · 2 hit papers
19 papers, 4.0k citations indexed

About

Jacqueline Maciazek is a scholar working on Neurology, Immunology and Allergy and Rheumatology. According to data from OpenAlex, Jacqueline Maciazek has authored 19 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Neurology, 5 papers in Immunology and Allergy and 4 papers in Rheumatology. Recurrent topics in Jacqueline Maciazek's work include Cerebrovascular and genetic disorders (13 papers), Cell Adhesion Molecules Research (5 papers) and Moyamoya disease diagnosis and treatment (4 papers). Jacqueline Maciazek is often cited by papers focused on Cerebrovascular and genetic disorders (13 papers), Cell Adhesion Molecules Research (5 papers) and Moyamoya disease diagnosis and treatment (4 papers). Jacqueline Maciazek collaborates with scholars based in France, United States and Italy. Jacqueline Maciazek's co-authors include Elisabeth Tournier‐Lasserve, Anne Joutel, Hugues Chabriat, Jean Weissenbach, Valérie Domenga, Katayoun Vahedi, Corinne Cruaud, Christophe Corpechot, Anne Ducros and Marie Germaine Bousser and has published in prestigious journals such as Nature, The Lancet and Nature Genetics.

In The Last Decade

Jacqueline Maciazek

19 papers receiving 3.9k 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.

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

1996 1.5k citations Anne Joutel, Christophe Corpechot et al. Nature profile →
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

1997 500 citations Anne Joutel, Katayoun Vahedi et al. The Lancet profile →

Peers

Countries citing papers authored by Jacqueline Maciazek

Since Specialization

Citations

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

Fields of papers citing papers by Jacqueline Maciazek

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacqueline Maciazek

This figure shows the co-authorship network connecting the top 25 collaborators of Jacqueline Maciazek. A scholar is included among the top collaborators of Jacqueline Maciazek 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 Jacqueline Maciazek. Jacqueline Maciazek is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	A novel hereditary small vessel disease of the brain 2006 ·Annals of Neurology ·Steve Verreault, Anne Joutel, Florence Riant, (unknown), Mário Rui Silva, Jacqueline Maciazek, Elisabeth Tournier‐Lasserve, Marie‐Germaine Bousser, Hugues Chabriat	21
2	Genotype–phenotype correlations in cerebral cavernous malformations patients 2006 ·Annals of Neurology ·Christian Denier, Pierre Labauge, Françoise Bergametti, Florence Marchelli, Florence Riant, (unknown), Jacqueline Maciazek, Éric Vicaut, L. Brunereau, Elisabeth Tournier‐Lasserve	171
3	ATP1A2 mutations in 11 families with familial hemiplegic migraine 2005 ·Human Mutation ·Florence Riant, Maurizio De Fusco, Paolo Aridon, Anne Ducros, (unknown), Florence Marchelli, Jacqueline Maciazek, Marie Germaine Bousser, Giorgio Casari, Elisabeth Tournier‐Lasserve	85
4	Notch3 is required for arterial identity and maturation of vascular smooth muscle cells 2004 ·Genes & Development ·Valérie Domenga, (unknown), Pierre Lacombe, (unknown), Jacqueline Maciazek, Luke T. Krebs, Bernard Klonjkowski, Eliane Berrou, Mathias Mericskay, Zhenlin Li, Elisabeth Tournier‐Lasserve, Thomas Gridley, Anne Joutel	415
5	Impaired Vascular Mechanotransduction in a Transgenic Mouse Model of CADASIL Arteriopathy 2004 ·Stroke ·Caroline Dubroca, Pierre Lacombe, Valérie Domenga, Jacqueline Maciazek, Bernard Lévy, Elisabeth Tournier‐Lasserve, Anne Joutel, Daniel Henrion	68
6	Clinical features of cerebral cavernous malformations patients with KRIT1 mutations 2003 ·Annals of Neurology ·Christian Denier, Pierre Labauge, L. Brunereau, Florence Riant, Florence Marchelli, (unknown), Michaelle Cécillon, Jacqueline Maciazek, Anne Joutel, Elisabeth Tournier‐Lasserve	73
7	Transgenic Mice Expressing Mutant Notch3 Develop Vascular Alterations Characteristic of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 2003 ·American Journal Of Pathology ·M M Ruchoux, Valérie Domenga, (unknown), Jacqueline Maciazek, (unknown), Elisabeth Tournier‐Lasserve, Anne Joutel	172
8	Spectrum and expression analysis of KRIT1 mutations in 121 consecutive and unrelated patients with Cerebral Cavernous Malformations 2002 ·European Journal of Human Genetics ·(unknown), Florence Riant, Christian Denier, Pierre Labauge, Michaelle Cécillon, Jacqueline Maciazek, Anne Joutel, Sophie Laberge, Elisabeth Tournier‐Lasserve	83
9	Evaluation of DHPLC analysis in mutational scanning ofNotch3, a gene with a high G-C content 2000 ·Human Mutation ·Jean-Louis Escary, (unknown), Jacqueline Maciazek, Mark Lathrop, Elisabeth Tournier‐Lasserve, Anne Joutel	40
10	Evaluation of DHPLC analysis in mutational scanning of Notch3, a gene with a high G-C content 2000 ·Human Mutation ·Jean-Louis Escary, Michaelle Cécillon, Jacqueline Maciazek, Mark Lathrop, Elisabeth Tournier‐Lasserve, Anne Joutel	1
11	[CADASIL: genetics and physiopathology]. 2000 ·PubMed ·Anne Joutel, (unknown), Hugues Chabriat, Katayoun Vahedi, F. Andreux, (unknown), Michaelle Cécillon, Jacqueline Maciazek, (unknown), Elisabeth Tournier‐Lasserve	8
12	Genetic heterogeneity and absence of founder effect in a series of 36 French cerebral cavernous angiomas families 1999 ·European Journal of Human Genetics ·Sophie Laberge, Pierre Labauge, (unknown), Jacqueline Maciazek, Elisabeth Tournier‐Lasserve	22
13	Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients breakdown → 1997 ·The Lancet ·Anne Joutel, Katayoun Vahedi, Christophe Corpechot, Alain Troesch, Hugues Chabriat, (unknown), Corinne Cruaud, Jacqueline Maciazek, Jean Weissenbach, Marie‐Germaine Bousser, Jean‐François Bach, Elisabeth Tournier‐Lasserve	500
14	Notch3 Mutations in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL), a Mendelian Condition Causing Stroke and Vascular Dementia 1997 ·Annals of the New York Academy of Sciences ·Anne Joutel, Christophe Corpechot, Anne Ducros, Katayoun Vahedi, Hugues Chabriat, (unknown), Sonia Alamowitch, Valérie Domenga, (unknown), (unknown), Jacqueline Maciazek, (unknown), Corinne Cruaud, Emmanuel‐Alain Cabanis, (unknown), Jean Weissenbach, J F Bach, M. G. Bousser, Elisabeth Tournier‐Lasserve	80
15	Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia breakdown → 1996 ·Nature ·Anne Joutel, Christophe Corpechot, Anne Ducros, Katayoun Vahedi, Hugues Chabriat, (unknown), Sonia Alamowitch, Valérie Domenga, (unknown), (unknown), Jacqueline Maciazek, (unknown), Corinne Cruaud, Emmanuel‐Alain Cabanis, (unknown), Jean Weissenbach, J F Bach, Marie Germaine Bousser, Elisabeth Tournier‐Lasserve	1492
16	[Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19]. 1994 ·PubMed ·Anne Joutel, M.G. Bousser, Valérie Biousse, Pierre Labauge, Hugues Chabriat, A Nibbio, Jacqueline Maciazek, Birgit Meyer, Marie‐Anne Bach, J. Weissenbach	4
17	Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12 1993 ·Nature Genetics ·Elisabeth Tournier‐Lasserve, Anne Joutel, Judith Melki, Jean Weissenbach, G.M. Lathrop, Hugues Chabriat, (unknown), E.A. Cabanis, Magalie Baudrimont, Jacqueline Maciazek, Marie‐Anne Bach, M G Bousser	423
18	A gene for familial hemiplegic migraine maps to chromosome 19 1993 ·Nature Genetics ·Anne Joutel, Marie‐Germaine Bousser, Valérie Biousse, Pierre Labauge, Hugues Chabriat, A Nibbio, Jacqueline Maciazek, (unknown), Marie‐Anne Bach, Jean Weissenbach, G.M. Lathrop, Elisabeth Tournier‐Lasserve	269
19	T cell response to myelin basic protein epitopes in multiple sclerosis patients and healthy subjects 1991 ·European Journal of Immunology ·Roland Liblau, Elisabeth Tournier‐Lasserve, Jacqueline Maciazek, (unknown), O. Siffert, George A. Hashim, Marie‐Anne Bach	59

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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