Luitgard M. Neumann

3.6k total citations
46 papers, 1.7k citations indexed

About

Luitgard M. Neumann is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Luitgard M. Neumann has authored 46 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 14 papers in Molecular Biology and 12 papers in Surgery. Recurrent topics in Luitgard M. Neumann's work include Connective tissue disorders research (13 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic Syndromes and Imprinting (3 papers). Luitgard M. Neumann is often cited by papers focused on Connective tissue disorders research (13 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic Syndromes and Imprinting (3 papers). Luitgard M. Neumann collaborates with scholars based in Germany, United States and Switzerland. Luitgard M. Neumann's co-authors include Peter N. Robinson, Heidemarie Neitzel, Thomas Rosenberg, Frank Tiecke, Patrick Booms, Marc Trimborn, André Reis, Karl Sperling, Reinhard Ullmann and Hans‐Hilger Ropers and has published in prestigious journals such as The American Journal of Human Genetics, American Journal of Neuroradiology and Journal of Medical Genetics.

In The Last Decade

Luitgard M. Neumann

44 papers receiving 1.6k citations

Peers

Countries citing papers authored by Luitgard M. Neumann

Since Specialization

Citations

This map shows the geographic impact of Luitgard M. 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 M. 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 M. Neumann more than expected).

Fields of papers citing papers by Luitgard M. Neumann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luitgard M. Neumann

This figure shows the co-authorship network connecting the top 25 collaborators of Luitgard M. Neumann. A scholar is included among the top collaborators of Luitgard M. 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 M. Neumann. Luitgard M. 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	No increase of biopsy rates despite high rates of probable eosinophilic esophagitis in patients with esophageal food impaction 2025 ·Wiener klinische Wochenschrift ·Luitgard M. Neumann, (unknown), Lili Kazemi-Shirazi, Michael Trauner, Christian Primas, (unknown), (unknown), (unknown), (unknown), Clemens Dejaco, Walter Reinisch, Gottfried Novacek, Philipp Schreiner	0
2	TheFBN2gene: new mutations, locus-specific database (Universal Mutation DatabaseFBN2), and genotype-phenotype correlations 2008 ·Human Mutation ·(unknown), (unknown), (unknown), Dalil Hamroun, Laurence Faivre, Guillaume Jondeau, (unknown), Luitgard M. Neumann, Élodie Gautier, Christine Binquet, Cheryl L. Maslen, Maurice Godfrey, Prateek Gupta, Dianna M. Milewicz, Cathérine Boileau, Mireille Claustres, Christophe Béroud, Gwenaëlle Collod‐Béroud	46
3	Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome 2007 ·The American Journal of Human Genetics ·Eva Klopocki, Harald Schulze, Gabriele Strauß, Claus‐Eric Ott, Judith G. Hall, (unknown), (unknown), Lynn Greenhalgh, Ruth Newbury‐Ecob, Luitgard M. Neumann, R. Habenicht, Rainer König, E Seemanová, André Mégarbané, Hans‐Hilger Ropers, Reinhard Ullmann, Denise Horn, Stefan Mundlos	201
4	Okuläre Manifestationen und chirurgische Ergebnisse beim Marfan-Syndrom 2006 ·Der Ophthalmologe ·Markus S. Ladewig, Peter N. Robinson, Luitgard M. Neumann, Frank G. Holz, Michael Foerster	14
5	Dyggve–Melchior–Clausen syndrome and Smith–McCort dysplasia: Clinical and molecular findings in three families supporting genetic heterogeneity in Smith–McCort dysplasia 2006 ·American Journal of Medical Genetics Part A ·Luitgard M. Neumann, Vincent El Ghouzzi, Vincent Paupe, Hans‐Peter Weber, (unknown), (unknown), (unknown), (unknown), Ertan Mayatepek, Jörg Pelz, Valérie Cormier‐Daire	21
6	Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13 2006 ·Cytogenetic and Genome Research ·H. Tönnies, (unknown), (unknown), Heike Starke, Heidemarie Neitzel, Luitgard M. Neumann	6
7	Ulnar–mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene 2006 ·European Journal of Human Genetics ·Eva Klopocki, Luitgard M. Neumann, Holger Tönnies, Hans‐Hilger Ropers, Stefan Mundlos, Reinhard Ullmann	34
8	Restrictive Dermopathy Associated With Transposition of the Great Arteries and Microcolon 2005 ·Archives of Dermatology ·Sven Armbrust, Rolf Hoffmann, Frank Jochum, Luitgard M. Neumann, Christoph Fusch	6
9	Mutations in Microcephalin Cause Aberrant Regulation of Chromosome Condensation 2004 ·The American Journal of Human Genetics ·Marc Trimborn, Sandra Bell, (unknown), Yasmin Abdul Rashid, Hussain Jafri, Paul Griffiths, Luitgard M. Neumann, Alice Krebs, André Reis, Karl Sperling, Heidemarie Neitzel, Andrew P. Jackson	190
10	Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: An autosomal recessive syndrome 2004 ·American Journal of Medical Genetics Part A ·Martin Zenker, (unknown), Thomas Lennert, Susanne Pitz, (unknown), (unknown), Jörg Dötsch, André Reis, H Müntefering, Luitgard M. Neumann	88
11	Ehlers-Danlos syndrome type VI with cystic malformations of the meninges in a 7-year-old girl 2004 ·European Journal of Pediatrics ·Irene Brunk, (unknown), Chrysanthy Ikonomidou, (unknown), Luitgard M. Neumann	12
12	Prenatal Diagnosis of Alagille Syndrome 2004 ·Journal of Pediatric Gastroenterology and Nutrition ·Heiko Witt, Luitgard M. Neumann, Oswin Grollmuss, W. A. P. Luck, (unknown)	2
13	Prenatal Diagnosis of Alagille Syndrome 2003 ·Journal of Pediatric Gastroenterology and Nutrition ·Heiko Witt, Luitgard M. Neumann, (unknown), W. A. P. Luck, (unknown)	6
14	Survival to adulthood and dominant inheritance of platyspondylic skeletal dysplasia, Torrance-Luton type 2003 ·Pediatric Radiology ·Luitgard M. Neumann, (unknown), Markus Uhl, (unknown), Bernhard Zabel, (unknown)	14
15	Congenital disorder of glycosylation type 1a in a macrosomic 16-month-old boy with an atypical phenotype and homozygosity of the N216I mutation 2003 ·European Journal of Pediatrics ·Luitgard M. Neumann, Arpad von Moers, Jürgen Kunze, Oliver Blankenstein, Thorsten Marquardt	10
16	Atlantoaxial instability in Dyggve-Melchior-Clausen syndrome 2002 ·Journal of Neurosurgery Spine ·Frank Kandziora, Luitgard M. Neumann, Klaus John Schnake, Cyrus Khodadadyan-Klostermann, (unknown), Norbert Haas, Thomas Mittlmeier	7
17	Premature Chromosome Condensation in Humans Associated with Microcephaly and Mental Retardation: A Novel Autosomal Recessive Condition 2002 ·The American Journal of Human Genetics ·Heidemarie Neitzel, Luitgard M. Neumann, Detlev Schindler, (unknown), Holger Tönnies, Marc Trimborn, Alice Krebsová, (unknown), Karl Sperling	82
18	Mutations of FBN1 and genotype-phenotype correlations in Marfan syndrome and related fibrillinopathies 2002 ·Human Mutation ·Peter N. Robinson, Patrick Booms, (unknown), Markus S. Ladewig, Luitgard M. Neumann, (unknown), Reinhard Pregla, Frank Tiecke, Thomas Rosenberg	143
19	Retinal angiomatosis and von Hippel-Lindau disease 2000 ·Graefe s Archive for Clinical and Experimental Ophthalmology ·KM Kreusel, Nikolaos E. Bechrakis, (unknown), Luitgard M. Neumann, H. P. H. Neumann, M. H. Foerster	21
20	Compression neuropathy of the common peroneal nerve caused by a ganglion 1994 ·Microsurgery ·(unknown), Luitgard M. Neumann, Simon P. Frostick	22

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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