Luitgard Graul‐Neumann

2.8k total citations
46 papers, 884 citations indexed

About

Luitgard Graul‐Neumann is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Luitgard Graul‐Neumann has authored 46 papers receiving a total of 884 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 28 papers in Genetics and 7 papers in Cell Biology. Recurrent topics in Luitgard Graul‐Neumann's work include Genomic variations and chromosomal abnormalities (10 papers), Connective tissue disorders research (6 papers) and Cleft Lip and Palate Research (5 papers). Luitgard Graul‐Neumann is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Connective tissue disorders research (6 papers) and Cleft Lip and Palate Research (5 papers). Luitgard Graul‐Neumann collaborates with scholars based in Germany, France and Poland. Luitgard Graul‐Neumann's co-authors include Eva Klopocki, Peter N. Robinson, Sabine Rudnik‐Schöneborn, Klaus Zerres, Eberhard Passarge, Denise Horn, Sven Armbrust, Anita Rauch, Silke Vogelgesang and Christoph Fusch and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Endocrinology and Journal of Medical Genetics.

In The Last Decade

Luitgard Graul‐Neumann

44 papers receiving 840 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luitgard Graul‐Neumann Germany 19 539 457 128 97 86 46 884
Luís Garcia Alonso Brazil 17 541 1.0× 621 1.4× 73 0.6× 112 1.2× 107 1.2× 56 1.1k
José‐Mario Capo‐Chichi Canada 14 515 1.0× 414 0.9× 99 0.8× 61 0.6× 74 0.9× 38 974
Ghislaine Plessis France 18 431 0.8× 341 0.7× 129 1.0× 103 1.1× 46 0.5× 31 810
Isabelle Thiffault United States 23 822 1.5× 482 1.1× 97 0.8× 67 0.7× 88 1.0× 65 1.4k
Jeroen Schoots Netherlands 11 451 0.8× 281 0.6× 244 1.9× 120 1.2× 77 0.9× 14 854
Olaf Rittinger Austria 17 433 0.8× 384 0.8× 74 0.6× 66 0.7× 45 0.5× 40 785
Emma Clement United Kingdom 16 968 1.8× 294 0.6× 217 1.7× 85 0.9× 141 1.6× 37 1.3k
Kristiina Avela Finland 17 633 1.2× 402 0.9× 49 0.4× 74 0.8× 66 0.8× 34 1.1k
Rodger Palmer United Kingdom 13 397 0.7× 494 1.1× 78 0.6× 76 0.8× 69 0.8× 20 915
Pagon Ra United States 6 450 0.8× 260 0.6× 70 0.5× 55 0.6× 44 0.5× 291 791

Countries citing papers authored by Luitgard Graul‐Neumann

Since Specialization
Citations

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

Fields of papers citing papers by Luitgard Graul‐Neumann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Luitgard Graul‐Neumann. 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 Luitgard Graul‐Neumann. The network helps show where Luitgard Graul‐Neumann may publish in the future.

Co-authorship network of co-authors of Luitgard Graul‐Neumann

This figure shows the co-authorship network connecting the top 25 collaborators of Luitgard Graul‐Neumann. A scholar is included among the top collaborators of Luitgard Graul‐Neumann 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 Luitgard Graul‐Neumann. Luitgard Graul‐Neumann 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.
Kloth, Katja, Luitgard Graul‐Neumann, Katharina Hermann, et al.. (2021). More evidence on TRIO missense mutations in the spectrin repeat domain causing severe developmental delay and recognizable facial dysmorphism with macrocephaly. Neurogenetics. 22(3). 221–224. 3 indexed citations
2.
Boschann, Felix, Björn Fischer‐Zirnsak, Thomas F. Wienker, et al.. (2020). An intronic splice site alteration in combination with a large deletion affecting VPS13B (COH1) causes Cohen syndrome. European Journal of Medical Genetics. 63(9). 103973–103973. 6 indexed citations
3.
Niceta, Marcello, Domenico Barbuti, Neerja Gupta, et al.. (2019). Skeletal abnormalities are common features in Aymé‐Gripp syndrome. Clinical Genetics. 97(2). 362–369. 10 indexed citations
4.
Graul‐Neumann, Luitgard, Martin A. Mensah, Eva Klopocki, et al.. (2018). Biallelic intragenic deletion in MASP1 in an adult female with 3MC syndrome. European Journal of Medical Genetics. 61(7). 363–368. 13 indexed citations
5.
Graul‐Neumann, Luitgard, et al.. (2018). Clinical report of 8 patients with 49,XXXXY syndrome: Delineation of the facial gestalt and depiction of the clinical spectrum. European Journal of Medical Genetics. 62(3). 210–216. 12 indexed citations
6.
Chantot‐Bastaraud, Sandra, Frédéric Brioude, Matthias Begemann, et al.. (2017). Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction. Molecular Cytogenetics. 10(1). 28–28. 20 indexed citations
7.
Pozojevic, Jelena, Ilaria Parenti, Luitgard Graul‐Neumann, et al.. (2017). Novel mosaic variants in two patients with Cornelia de Lange syndrome. European Journal of Medical Genetics. 61(11). 680–684. 7 indexed citations
8.
Passarge, Eberhard, Peter N. Robinson, & Luitgard Graul‐Neumann. (2016). Marfanoid–progeroid–lipodystrophy syndrome: a newly recognized fibrillinopathy. European Journal of Human Genetics. 24(9). 1244–1247. 26 indexed citations
9.
Southgate, Laura, Maja Sukalo, Edward J. Taylor, et al.. (2015). Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams–Oliver Syndrome With Variable Cardiac Anomalies. Circulation Cardiovascular Genetics. 8(4). 572–581. 70 indexed citations
10.
Zweier, Christiane, Olaf Rittinger, Ingrid Bader, et al.. (2014). Females with de novo aberrations in PHF6: Clinical overlap of Borjeson–Forssman–Lehmann with Coffin–Siris syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 166(3). 290–301. 20 indexed citations
11.
Zweier, Christiane, Cornelia Kraus, Louise Brueton, et al.. (2013). A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype. Journal of Medical Genetics. 50(12). 838–847. 32 indexed citations
12.
Zirn, Birgit, Luitgard Graul‐Neumann, M. Suckfüll, et al.. (2013). Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnostics. BMJ Open. 3(3). e001917–e001917. 38 indexed citations
13.
Solomon, Benjamin D., et al.. (2012). Holoprosencephaly–polydactyly/pseudotrisomy 13. Clinical Dysmorphology. 21(4). 183–190. 8 indexed citations
14.
Adolphs, Nicolai, Éric Arnaud, Luitgard Graul‐Neumann, et al.. (2012). The oculo-auriculo-fronto-nasal syndrome (OAFNS) – Description of a rare and complex craniofacial deformity and its interdisciplinary management before school age. Journal of Cranio-Maxillofacial Surgery. 40(8). 668–674. 3 indexed citations
15.
16.
Graul‐Neumann, Luitgard, Karola Stieler, Ulrike Blume‐Peytavi, & Andreas Tzschach. (2009). Autosomal dominant inheritance in a large family with focal facial dermal dysplasia (Brauer–Setleis syndrome). American Journal of Medical Genetics Part A. 149A(4). 746–750. 6 indexed citations
17.
Krause, Lothar, et al.. (2009). Familienuntersuchungen bei Patienten mit Angiomatosis retinae. Klinische Monatsblätter für Augenheilkunde. 226(11). 939–943. 1 indexed citations
18.
Klopocki, Eva, Ran Wei, Christiane Bommer, et al.. (2009). De novo 9 Mb deletion of 6q23.2q24.1 disrupting the gene EYA4 in a patient with sensorineural hearing loss, cardiac malformation, and mental retardation. European Journal of Medical Genetics. 52(6). 450–453. 9 indexed citations
19.
Graul‐Neumann, Luitgard, et al.. (2008). Highly variable cutis laxa resulting from a dominant splicing mutation of the elastin gene. American Journal of Medical Genetics Part A. 146A(8). 977–983. 37 indexed citations
20.
Klopocki, Eva, Luitgard Graul‐Neumann, Ulrike Grieben, et al.. (2007). A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH. European Journal of Pediatrics. 167(8). 903–908. 43 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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