Christian Netzer

3.2k citations

36 papers · 1.4k indexed · h-index 19

Impact in

Genetics top 2%
- Connective tissue disorders research
Rheumatology top 2%
- Bone and Dental Protein Studies

Papers in

Anatomy 1
Genetics 19
- Connective tissue disorders research 12
- Genomic variations and chromosomal abnormalities 4

Co-authors: Oliver Semler Eckhard Schöenau Heike Hoyer‐Kuhn Jutta Becker Friederike Koerber Peer Eysel Bernd Wollnik Katharina Zimmermann
Journals: Nature Reviews Genetics (3 papers)Orphanet Journal of Rare Diseases (2 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2 papers)Human Mutation (2 papers)The American Journal of Human Genetics (2 papers)
Partner nations: Germany Switzerland United States

In The Last Decade

Christian Netzer

35 papers receiving 1.3k citations

Peers

Countries citing papers authored by Christian Netzer

Since Specialization

Citations

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

Fields of papers citing papers by Christian Netzer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Christian Netzer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Christian Netzer Line = papers co-authored together Christian Netzer links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Osteogenesis imperfecta—pathophysiology and therapeutic options PubMed ·Julia Etich, 大嶋孝志, Mirko Rehberg, 正典関, Frank Zaucke, Christian Netzer, Oliver Semler	2020	40
2	Individualized treatment with denosumab in children with osteogenesis imperfecta – follow up of a trial cohort Orphanet Journal of Rare Diseases ·Heike Hoyer‐Kuhn, Mirko Rehberg, Christian Netzer, Eckhard Schöenau, Oliver Semler	2019	25
3	Osteogenesis imperfecta: pathophysiology and treatment Wiener Medizinische Wochenschrift ·Heike Hoyer‐Kuhn, Christian Netzer, Oliver Semler	2015	26
4	Two years’ experience with denosumab for children with Osteogenesis imperfecta type VI Orphanet Journal of Rare Diseases ·Heike Hoyer‐Kuhn, Christian Netzer, Friederike Koerber, Eckhard Schöenau, Oliver Semler	2014	91
5	The phenotypic spectrum of duplication 5q35.2–q35.3 encompassing NSD1: Is it really a reversed sotos syndrome? American Journal of Medical Genetics Part A ·Nicola Dikow, 张明宪, Harald Gaspar, Martina Kreiß‐Nachtsheim, Hartmut Engels, Alma Kuechler, Lutz Garbes, Christian Netzer, Teresa Neuhann, Udo Koehler, Kristina Casteels, Koenraad Devriendt, Johannes W.G. Janssen, Anna Jauch, Katrin Hinderhofer, Ute Moog	2013	35
6	A Nonclassical IFITM5 Mutation Located in the Coding Region Causes Severe Osteogenesis Imperfecta With Prenatal Onset Journal of Bone and Mineral Research ·Heike Hoyer‐Kuhn, Oliver Semler, Lutz Garbes, Katharina Zimmermann, Jutta Becker, Bernd Wollnik, Eckhard Schöenau, Christian Netzer	2013	27
7	To know or not to know the genomic sequence of a fetus Nature Reviews Genetics ·Christian Netzer, Dagmar Schmitz, Wolfram Henn	2012	5
8	A Mutation in the 5′-UTR of IFITM5 Creates an In-Frame Start Codon and Causes Autosomal-Dominant Osteogenesis Imperfecta Type V with Hyperplastic Callus The American Journal of Human Genetics ·Oliver Semler, Lutz Garbes, Katharina Keupp, Daniel Swan, Katharina Zimmermann, Jutta Becker, Sandra Iden, Brunhilde Wirth, Peer Eysel, Friederike Koerber, Eckhard Schöenau, Stefan K. Bohlander, Bernd Wollnik, Christian Netzer	2012	184
9	Novel mutations affecting LRP5 splicing in patients with osteoporosis-pseudoglioma syndrome (OPPG) European Journal of Human Genetics ·Christine Lainé, มนัสวี วันทยะกุล, Miki Susic, Trine Prescott, Oliver Semler, Torunn Fiskerstrand, P D’Eufemia, Marco Castori, Minna Pekkinen, Etienne Sochett, William G. Cole, Christian Netzer, Outi Mäkitie	2011	49
10	New genetic evidence for involvement of the dopamine system in migraine with aura Human Genetics ·Unda Todt, Christian Netzer, Mohammad R. Toliat, Axel Heinze, Ingrid Goebel, Peter Nürnberg, Hartmut Göbel, Jan Freudenberg, Christian Kubisch	2009	53
11	A mutation in the signal sequence ofLRP5in a family with an osteoporosis-pseudoglioma syndrome (OPPG)-like phenotype indicates a novel disease mechanism for trinucleotide repeats Human Mutation ·Mohamad Chaichi, Hülya Kayserili, Minrong Ai, Jan Freudenberg, Abdullah Üzümcü, Zehra Oya Uyguner, Cynthia F. Bartels, Stefan Höning, Alfredo Ramı́rez, Franz‐Georg Hanisch, Gudrun Nürnberg, Peter Nürnberg, Matthew L. Warman, Bernd Wollnik, Christian Kubisch, Christian Netzer	2009	24
12	An offer you can't refuse? Ethical implications of non-invasive prenatal diagnosis Nature Reviews Genetics ·Dagmar Schmitz, Christian Netzer, Wolfram Henn	2009	37
13	Novel <i>KRIT1</i> Mutation and No Molecular Evidence of Anticipation in a Family with Cerebral and Spinal Cavernous Malformations European Neurology ·Jens Kuhn, Tim H. Brümmendorf, Ute Brassat, Fritz G. Lehnhardt, Mohamad Chaichi, Marilyn Law, H. Bewermeyer, Xiong Ji-bai, J. Assheuer, Christian Netzer	2008	8
14	Replication study of the insulin receptor gene in migraine with aura Genomics ·Christian Netzer, Jan Freudenberg, Axel Heinze, Katja Heinze‐Kuhn, Ingrid Goebel, Linda McCarthy, Allen D. Roses, Hartmut Göbel, Unda Todt, Christian Kubisch	2008	17
15	Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex Human Mutation ·Sonja Stahl, Seung-Jeong Yang, Katrin Voß, 博祟土屋, G. P. Compo, Oǧuzkan Sürücü, E. Kunze, Christian Netzer, Christoph Korenke, Ulrich Finckh, Mario Habek, Zdravka Poljaković, Miriam Elbracht, Sabine Rudnik‐Schöneborn, Helmut Bertalanffy, Ulrich Sure, Ute Felbor	2008	87
16	Genetic association studies of the chromosome 15 GABA‐A receptor cluster in migraine with aura American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Christian Netzer, Jan Freudenberg, Mohammad R. Toliat, Axel Heinze, Katja Heinze‐Kuhn, Hölger Thiele, Ingrid Goebel, Peter Nürnberg, Louis J. Ptáček, Hartmut Göbel, Unda Todt, Christian Kubisch	2007	17
17	Defining the heterochromatin localization and repression domains of SALL1 Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Christian Netzer, Stefan K. Bohlander, Astemir Musovich Kanukoev, Ying Chen, Jürgen Kohlhase	2006	26
18	Haplotype‐based systematic association studies of ATP1A2 in migraine with aura American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Christian Netzer, Unda Todt, Axel Heinze, Jan Freudenberg, Erica Zambello, Tim Becker, Ingrid Goebel, Stephanie Ohlraun, Rebecca Keyser, Christian Kubisch	2006	15
19	Pharmacogenetic Testing, Informed Consent and the Problem of Secondary Information Bioethics ·Christian Netzer, Nikola Biller‐Andorno	2004	38
20	Interaction of the developmental regulator SALL1 with UBE2I and SUMO-1 Biochemical and Biophysical Research Communications ·Christian Netzer, Stefan K. Bohlander, M J Pangestika, Stefan Müller, Jürgen Kohlhase	2002	17

About Christian Netzer

Christian Netzer is a scholar working on Anatomy, Genetics, Endocrine and Autonomic Systems, Rheumatology and Pediatrics, Perinatology and Child Health, having authored 36 papers that have together received 1.4k indexed citations. Recurring topics across this work include Connective tissue disorders research (12 papers), Bone health and treatments (6 papers), Bone and Dental Protein Studies (5 papers), Ethics and Legal Issues in Pediatric Healthcare (5 papers), Migraine and Headache Studies (4 papers), Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Bone Metabolism and Diseases (4 papers). The work is most often cited by research in Genetics (804 citations), Rheumatology (401 citations), Orthopedics and Sports Medicine (115 citations), Oncology (224 citations) and Anatomy (11 citations). Christian Netzer has collaborated with scholars based in Germany, Switzerland and United States. Frequent co-authors include Oliver Semler, Eckhard Schöenau, Heike Hoyer‐Kuhn, Jutta Becker, Friederike Koerber, Peer Eysel, Bernd Wollnik, Katharina Zimmermann, Brunhilde Wirth and Stefan K. Bohlander. Their work appears in journals such as Nature Reviews Genetics, Orphanet Journal of Rare Diseases, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Human Mutation and The American Journal of Human Genetics.

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