Hermann‐Josef Lüdecke

3.9k citations

39 papers · 1.8k indexed · h-index 19

Molecular Biology top 10%
Genetics top 2%
Rheumatology top 2%
Pulmonary and Respiratory Medicine top 10%
Oral Surgery top 2%

Co-authors: Bernhard Horsthemke Uwe Claussen Gabriele Senger Dagmar Wieczorek Brendan Lee Michael J. Wagner Jung Ahn William A. Horton
Topics: Genomic variations and chromosomal abnormalities (10 papers)Genetic Syndromes and Imprinting (5 papers)RNA regulation and disease (5 papers)
Cited by: Oral Surgery Genetics Rheumatology
Journals: Nature Nucleic Acids Research Journal of Biological Chemistry
Partner nations: Germany United States Belgium

In The Last Decade

Hermann‐Josef Lüdecke

39 papers receiving 1.8k citations

Peers

Countries citing papers authored by Hermann‐Josef Lüdecke

Since Specialization

Citations

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

Fields of papers citing papers by Hermann‐Josef Lüdecke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hermann‐Josef Lüdecke. 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 Hermann‐Josef Lüdecke. The network helps show where Hermann‐Josef Lüdecke may publish in the future.

Co-authorship network of co-authors of Hermann‐Josef Lüdecke

This figure shows the co-authorship network connecting the top 25 collaborators of Hermann‐Josef Lüdecke. A scholar is included among the top collaborators of Hermann‐Josef Lüdecke 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 Hermann‐Josef Lüdecke. Hermann‐Josef Lüdecke 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	FGF9-Associated Multiple Synostoses Syndrome Type 3 in a Multigenerational Family 2023 ·Genes ·(unknown),Jörg Schaper,Simon Thelen,(unknown),Thomas Klenzner,K. Schaumann,Jasmin Beygo,Harald Surowy,Hermann‐Josef Lüdecke,Dagmar Wieczorek	2
2	Expanding the spectrum of EEF1D neurodevelopmental disorders: Biallelic variants in the guanine exchange domain 2022 ·Clinical Genetics ·Luisa Averdunk,Khalid Al‐Thihli,Harald Surowy,Hermann‐Josef Lüdecke,Matthias Drechsler,Gökhan Yiğit,Lukasz Smorag,(unknown),Yun Li,Janine Altmüller,(unknown),Michael Wallot,Peter Nürnberg,Bernd Wollnik,Rami Abou Jamra,Almundher Al‐Maawali,Dagmar Wieczorek	1
3	Maternal transmission of a mild Coffin–Siris syndrome phenotype caused by a SOX11 missense variant 2021 ·European Journal of Human Genetics ·(unknown),Gabriele Gillessen‐Kaesbach,Irina Hüning,Hermann‐Josef Lüdecke,Dagmar Wieczorek	4
4	The Macrophage Migration Inhibitory Factor (MIF) Promoter Polymorphisms (rs3063368, rs755622) Predict Acute Kidney Injury and Death after Cardiac Surgery 2020 ·Journal of Clinical Medicine ·Luisa Averdunk,Jürgen Bernhagen,(unknown),Harald Surowy,Hermann‐Josef Lüdecke,Sören Mucha,Patrick Meybohm,Dagmar Wieczorek,Lin Leng,Gernot Marx,David E. Leaf,Alexander Zarbock,Kai Zacharowski,(unknown),Richard Bucala,Christian Stoppe	13
5	New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome 2017 ·European Journal of Human Genetics ·Jasmin Beygo,(unknown),Gabriele Gillessen‐Kaesbach,Beate Albrecht,(unknown),Thomas Eggermann,Alexandra Gellhaus,Deniz Kanber,(unknown),Hermann‐Josef Lüdecke,Sabine Purmann,Eva Rossier,Johannes van de Nes,Ilse M. van der Werf,(unknown),Dagmar Wieczorek,Bernhard Horsthemke,Karin Buiting	31
6	De novo microdeletions and point mutations affecting SOX2 in three individuals with intellectual disability but without major eye malformations 2016 ·American Journal of Medical Genetics Part A ·(unknown),Hartmut Engels,Kirsten Cremer,Jessica Becker,Eva Wohlleber,Beate Albrecht,(unknown),Hermann‐Josef Lüdecke,Mohnish Suri,(unknown),Alessandra Renieri,Guido Kukuk,Thomas Wieland,Joris Andrieux,Tim M. Strom,Dagmar Wieczorek,Anne Dieux‐Coëslier,Alexander M. Zink	13
7	A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith–Wiedemann syndrome 2016 ·European Journal of Human Genetics ·Jasmin Beygo,Ivana Joksić,Tim M. Strom,Hermann‐Josef Lüdecke,Julia Kolarova,Reiner Siebert,Željko Miković,Bernhard Horsthemke,Karin Buiting	18
8	A novel large deletion of the ICR1 region including H19 and putative enhancer elements 2015 ·BMC Medical Genetics ·Helen Fryssira,(unknown),Deniz Kanber,Christalena Sofocleous,(unknown),Christina Kanaka‐Gantenbein,Flavia Cerrato,Hermann‐Josef Lüdecke,Susanne Bens,Andrea Riccio,Karin Buiting	6
9	A patient with a de-novo deletion 3p25.3 and features overlapping with Rubinstein–Taybi syndrome 2014 ·Clinical Dysmorphology ·Johanna Christina Czeschik,Beate Albrecht,Hülya Kayserili,Alma Kuechler,Nicholas Wagner,Dagmar Wieczorek,Hermann‐Josef Lüdecke	2
10	X-linked intellectual disability type Nascimento is a clinically distinct, probably underdiagnosed entity 2013 ·Orphanet Journal of Rare Diseases ·Johanna Christina Czeschik,Peter Bauer,Karin Buiting,Claudia Dufke,Encarna Guillén‐Navarro,Diana Johnson,Udo Koehler,Vanesa López‐González,Hermann‐Josef Lüdecke,Alison Male,Deborah Morrogh,Angelika Rieß,Andreas Tzschach,Dagmar Wieczorek,Alma Kuechler	17
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	Wide clinical variability in conditions with coarse facial features and hypertrichosis caused by mutations in ABCC9 2013 ·American Journal of Medical Genetics Part A ·Johanna Christina Czeschik,(unknown),Timm O. Goecke,Hermann‐Josef Lüdecke,Nicholas Wagner,Alma Kuechler,Dagmar Wieczorek	24
13	160 kb deletion in ISPD unmasking a recessive mutation in a patient with Walker–Warburg syndrome 2013 ·European Journal of Medical Genetics ·Johanna Christina Czeschik,Ute Hehr,Britta Hartmann,Hermann‐Josef Lüdecke,Thorsten Rosenbaum,Bernd Schweiger,Dagmar Wieczorek	18
14	Rheumatologic and neurological events in an elderly patient with tricho-rhino-phalangeal syndrome type I 2011 ·European Journal of Medical Genetics ·(unknown),Hermann‐Josef Lüdecke,Igor Sibon,Christophe Richez,Laurence Taine,Alexandra Foubert‐Samier,Benoı̂t Arveiler,Thierry Schaeverbeke,Didier Lacombe,François Tison,Cyril Goizet	6
15	Clinical and molecular characterization of a patient with Langer–Giedion syndrome and mosaic del(8)(q22.3q24.13) 2008 ·American Journal of Medical Genetics Part A ·Alan Shanske,Ankita Patel,(unknown),Brynn Levy,Hermann‐Josef Lüdecke	15
16	A family with autosomal dominant oculo-auriculo-vertebral spectrum 2006 ·Clinical Dysmorphology ·(unknown),Frank Majewski,Stefan Böhringer,Sven Fischer,Hermann‐Josef Lüdecke,Gabriele Gillessen‐Kaesbach,Dagmar Wieczorek	59
17	Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion 2002 ·American Journal of Medical Genetics ·Wim Wuyts,Dominique Roland,Hermann‐Josef Lüdecke,J. Wauters,(unknown),Wim Van Hul,Lionel Van Maldergem	29
18	Trichorhinophalangeal Syndrome Type I 2001 ·Archives of Dermatology ·Cornelia S. Seitz,Hermann‐Josef Lüdecke,Nicola Wagner,Eva‐Bettina Bröcker,Henning Hamm	21
19	Four RFLPs at the D8S42 locus 1990 ·Nucleic Acids Research ·Bernhard Horsthemke,(unknown),Hermann‐Josef Lüdecke	1
20	Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification 1989 ·Nature ·Hermann‐Josef Lüdecke,Gabriele Senger,Uwe Claussen,Bernhard Horsthemke	261

About Hermann‐Josef Lüdecke

Hermann‐Josef Lüdecke is a scholar working on Developmental Biology, Genetics and Genetics, having authored 39 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Genetic Syndromes and Imprinting (5 papers) and RNA regulation and disease (5 papers). The work is most often cited by research in Oral Surgery (248 citations), Genetics (864 citations) and Rheumatology (367 citations). Hermann‐Josef Lüdecke has collaborated with scholars based in Germany, United States and Belgium. Frequent co-authors include Bernhard Horsthemke, Uwe Claussen, Gabriele Senger, Dagmar Wieczorek, Brendan Lee, Michael J. Wagner, Jung Ahn, William A. Horton, Dan E. Wells and Beate Albrecht. Their work appears in journals such as Nature, Nucleic Acids Research and Journal of Biological Chemistry.

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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