Luitgard Graul‐Neumann

2.8k citations

46 papers · 884 indexed · h-index 19

Co-authors: Eva Klopocki Peter N. Robinson Sabine Rudnik‐Schöneborn Klaus Zerres Eberhard Passarge Denise Horn Sven Armbrust Anita Rauch
Topics: Genomic variations and chromosomal abnormalities (10 papers)Connective tissue disorders research (6 papers)Cleft Lip and Palate Research (5 papers)
Cited by: Genetics Molecular Biology
Journals: The Journal of Clinical Endocrinology & Metabolism Endocrinology Journal of Medical Genetics
Partner nations: Germany France Poland

In The Last Decade

Luitgard Graul‐Neumann

44 papers receiving 840 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	More evidence on TRIO missense mutations in the spectrin repeat domain causing severe developmental delay and recognizable facial dysmorphism with macrocephaly 2021 ·Neurogenetics ·Katja Kloth,Luitgard Graul‐Neumann,Katharina Hermann,Jessika Johannsen,Tatjana Bierhals,Fanny Kortüm	3
2	An intronic splice site alteration in combination with a large deletion affecting VPS13B (COH1) causes Cohen syndrome 2020 ·European Journal of Medical Genetics ·Felix Boschann,Björn Fischer‐Zirnsak,Thomas F. Wienker,Manuel Holtgrewe,Dominik Seelow,(unknown),(unknown),Raimund Fahsold,Denise Horn,Luitgard Graul‐Neumann	6
3	Skeletal abnormalities are common features in Aymé‐Gripp syndrome 2019 ·Clinical Genetics ·Marcello Niceta,Domenico Barbuti,Neerja Gupta,Carlos Ruggiero,Eduardo F. Tizzano,Luitgard Graul‐Neumann,Sabina Barresi,Gen Nishimura,Irene Valenzuela,(unknown),Paula Fernández‐Álvarez,Chiara Leoni,Christiane Zweier,Andreas Tzschach,Emilia Stellacci,Andrea Del Fattore,Bruno Dallapiccola,Giuseppe Zampino,Marco Tartaglia	10
4	Biallelic intragenic deletion in MASP1 in an adult female with 3MC syndrome 2018 ·European Journal of Medical Genetics ·Luitgard Graul‐Neumann,Martin A. Mensah,Eva Klopocki,Steffen Uebe,Arif B. Ekici,Christian T. Thiel,André Reis,Christiane Zweier	13
5	Clinical report of 8 patients with 49,XXXXY syndrome: Delineation of the facial gestalt and depiction of the clinical spectrum 2018 ·European Journal of Medical Genetics ·(unknown),(unknown),(unknown),Luitgard Graul‐Neumann,Birgit Köhler,(unknown),(unknown),(unknown),Martin Maurer,Birgit Zirn	12
6	Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction 2017 ·Molecular Cytogenetics ·Sandra Chantot‐Bastaraud,(unknown),Frédéric Brioude,Matthias Begemann,Miriam Elbracht,Luitgard Graul‐Neumann,Madeleine D. Harbison,Irène Netchine,Thomas Eggermann	20
7	Novel mosaic variants in two patients with Cornelia de Lange syndrome 2017 ·European Journal of Medical Genetics ·Jelena Pozojevic,Ilaria Parenti,Luitgard Graul‐Neumann,Sara Ruiz Gil,Erwan Watrin,Kerstin S. Wendt,Ralf Werner,Tim M. Strom,Gabriele Gillessen‐Kaesbach,Frank J. Kaiser	7
8	Marfanoid–progeroid–lipodystrophy syndrome: a newly recognized fibrillinopathy 2016 ·European Journal of Human Genetics ·Eberhard Passarge,Peter N. Robinson,Luitgard Graul‐Neumann	26
9	Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams–Oliver Syndrome With Variable Cardiac Anomalies 2015 ·Circulation Cardiovascular Genetics ·Laura Southgate,Maja Sukalo,(unknown),Edward J. Taylor,(unknown),Deborah Ruddy,Katie Snape,Bruno Dallapiccola,John Tolmie,Shelagh Joss,Francesco Brancati,M. Cristina Digilio,Luitgard Graul‐Neumann,Leonardo Salviati,Wiltrud Coerdt,Emmanuel Jacquemin,Wim Wuyts,Martin Zenker,Rajiv D. Machado,Richard C. Trembath	70
10	Females with de novo aberrations in PHF6: Clinical overlap of Borjeson–Forssman–Lehmann with Coffin–Siris syndrome 2014 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Christiane Zweier,Olaf Rittinger,Ingrid Bader,Siren Berland,Trevor Cole,Franziska Degenhardt,Nataliya Di Donato,Luitgard Graul‐Neumann,Juliane Hoyer,Sally Ann Lynch,(unknown),Dagmar Wieczorek	20
11	A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype 2013 ·Journal of Medical Genetics ·Christiane Zweier,Cornelia Kraus,Louise Brueton,Trevor Cole,Franziska Degenhardt,Hartmut Engels,Gabriele Gillessen‐Kaesbach,Luitgard Graul‐Neumann,Denise Horn,Juliane Hoyer,Walter Just,Anita Rauch,André Reis,Bernd Wollnik,Michael Zeschnigk,Hermann‐Josef Lüdecke,Dagmar Wieczorek	32
12	Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnostics 2013 ·BMJ Open ·(unknown),Birgit Zirn,Luitgard Graul‐Neumann,(unknown),M. Suckfüll,Annegret Buske,Axel Bohring,Christian Kubisch,Stefanie Vogt,Gertrud Strobl‐Wildemann,Marie T. Greally,Oliver Bartsch,Daniela Steinberger	38
13	Holoprosencephaly–polydactyly/pseudotrisomy 13 2012 ·Clinical Dysmorphology ·(unknown),Benjamin D. Solomon,Luitgard Graul‐Neumann,Heidemarie Neitzel,(unknown),Maximilian Muenke	8
14	The oculo-auriculo-fronto-nasal syndrome (OAFNS) – Description of a rare and complex craniofacial deformity and its interdisciplinary management before school age 2012 ·Journal of Cranio-Maxillofacial Surgery ·Nicolai Adolphs,Éric Arnaud,(unknown),Luitgard Graul‐Neumann,Gül Schmidt,Horst Menneking,Bodo Hoffmeister	3
15	Necrotizing soft tissue infection of the scalp after fronto-facial advancement by internal distraction in a 7-year old girl with Gorlin–Chaudhry–Moss syndrome – A case report 2011 ·Journal of Cranio-Maxillofacial Surgery ·Nicolai Adolphs,Martin Klein,(unknown),Luitgard Graul‐Neumann,Horst Menneking,Bodo Hoffmeister	8
16	Autosomal dominant inheritance in a large family with focal facial dermal dysplasia (Brauer–Setleis syndrome) 2009 ·American Journal of Medical Genetics Part A ·Luitgard Graul‐Neumann,Karola Stieler,Ulrike Blume‐Peytavi,Andreas Tzschach	6
17	Familienuntersuchungen bei Patienten mit Angiomatosis retinae 2009 ·Klinische Monatsblätter für Augenheilkunde ·(unknown),Lothar Krause,Luitgard Graul‐Neumann,Nikolaos E. Bechrakis,Hartmut P.H. Neumann,M. H. Foerster	1
18	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 2009 ·European Journal of Medical Genetics ·(unknown),Eva Klopocki,Ran Wei,Christiane Bommer,Stefan Mundlos,Luitgard Graul‐Neumann,Marc Trimborn	9
19	Highly variable cutis laxa resulting from a dominant splicing mutation of the elastin gene 2008 ·American Journal of Medical Genetics Part A ·Luitgard Graul‐Neumann,Ingrid Haußer,(unknown),Anita Rauch,Cornelia Kraus	37
20	A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH 2007 ·European Journal of Pediatrics ·Eva Klopocki,Luitgard Graul‐Neumann,Ulrike Grieben,Holger Tönnies,Hans‐Hilger Ropers,Denise Horn,Stefan Mundlos,Reinhard Ullmann	43

About Luitgard Graul‐Neumann

Luitgard Graul‐Neumann is a scholar working on Developmental Biology, Genetics and Immunology and Allergy, having authored 46 papers that have together received 884 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Connective tissue disorders research (6 papers) and Cleft Lip and Palate Research (5 papers). The work is most often cited by research in Genetics (457 citations), Genetics (128 citations) and Molecular Biology (539 citations). Luitgard Graul‐Neumann has collaborated with scholars based in Germany, France and Poland. Frequent 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. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, Endocrinology and Journal of Medical Genetics.

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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