Andreas Janecke

17.6k citations

132 papers · 4.4k indexed · h-index 37

Impact in

Sensory Systems top 1%
- Hearing, Cochlea, Tinnitus, Genetics
Genetics top 1%
- Connective tissue disorders research
- Genetics and Neurodevelopmental Disorders

Papers in

Genetics 48
- Digestive system and related health 10
- Genetics and Neurodevelopmental Disorders 9
- Connective tissue disorders research 8
- Genetic and Kidney Cyst Diseases 7
Gastroenterology 9
- Celiac Disease Research and Management 9

Co-authors: Thomas Müller Gerd Utermann Andreas Gal Robert Gruber Lukas A. Huber Heinz Zoller Barbara Günther Michael W. Hess
Journals: Human Mutation (10 papers)European Journal of Human Genetics (5 papers)Journal of Pediatric Gastroenterology and Nutrition (5 papers)Human Genetics (5 papers)The American Journal of Human Genetics (4 papers)
Partner nations: Austria Germany United States

In The Last Decade

Andreas Janecke

127 papers receiving 4.3k citations

Peers

Countries citing papers authored by Andreas Janecke

Since Specialization

Citations

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

Fields of papers citing papers by Andreas Janecke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Andreas Janecke, 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 Andreas Janecke Line = papers co-authored together Andreas Janecke links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	PERCC1 ‐Related Congenital Enteropathy Clinical Genetics ·Davide Gandolfi, Pia Karlsland Åkeson, Thomas Müller, Andreas Janecke	2024	0
2	Steatotic liver disease associated with 2,4-dienoyl-CoA reductase 1 deficiency International Journal of Obesity ·Benno Kohlmaier, Kristijan Skok, Carolin Lackner, Anna JMVan Der Sande, Thomas Müller, S. Sailer, Johannes Zschocke, Markus A. Keller, Alexander S. Knisely, Andreas Janecke	2024	0
3	The Recurrent E-Cadherin (CDH1) Mutation c.760G>A Causes Orofacial Clefts but Does Not Predispose to Hereditary Cancer Genes ·Liebwin Goßner, Dietmar Rieder, Thomas Müller, Andreas Janecke	2024	0
4	Leri–Weill Dyschondrosteosis Caused by a Leaky Homozygous SHOX Splice-Site Variant Genes ·Julia Vodopiutz, Ibon Alcorta, 이승숙, Franco Laccone, P C Mendelowitz, Tamela Mannes, Philipp Steinbauer, Andreas Janecke	2023	2
5	SLC5A1 Variants in Turkish Patients with Congenital Glucose-Galactose Malabsorption Genes ·Quan Minh Vu, Andreas Janecke, Yadnesh Chhand, Georg F. Vogel, 山下奈奈, Nuria Calle, Thomas Müller, Lukas A. Huber, Taras Valovka, Aysel Ünlüsoy Aksu	2023	3
6	MRI‐Based Iron Phenotyping and Patient Selection for Next‐Generation Sequencing of Non–Homeostatic Iron Regulator Hemochromatosis Genes Hepatology ·André Viveiros, Benedikt Schaefer, 三浦修司, Benjamin Henninger, Michaela Plaikner, Christian Kremser, André Franke, Sören Franzenburg, Marc P. Hoeppner, Reinhard Stauder, Andreas Janecke, Herbert Tilg, Heinz Zoller	2021	7
7	Three Novel EPCAM Variants Causing Tufting Enteropathy in Three Families Children ·Hasret Ayyıldız Civan, Nikolaos Poulianitis, Zoubir Nemouchi, Anna-Maria Schneider, Malte Cremer, Johannes A. Mayr, Rainer Rossi, Thomas Müller, Andreas Janecke	2021	4
8	Abnormal Rab11‐Rab8‐vesicles cluster in enterocytes of patients with microvillus inclusion disease Traffic ·Georg F. Vogel, Andreas Janecke, M.I. Dinator, Eeva Jason, Claudia Kemper, Sally G. Mitton, Sahar Mansour, Antje Ballauff, Joseph T. Roland, Amy C. Engevik, Ernest Cutz, Thomas Müller, James R. Goldenring, Lukas A. Huber, Michael W. Hess	2017	36
9	Homozygous SYNE1 mutation causes congenital onset of muscular weakness with distal arthrogryposis: a genotype–phenotype correlation European Journal of Human Genetics ·Matthias Baumann, Elisabeth Steichen‐Gersdorf, Birgit Krabichler, Britt‐Sabina Petersen, U. Weber, Wolfgang M. Schmidt, Johannes Zschocke, Thomas Müller, Reginald E. Bittner, Andreas Janecke	2016	30
10	Loss of dermatan sulfate epimerase (DSE) function results in musculocontractural Ehlers–Danlos syndrome Human Molecular Genetics ·Thomas Müller, Shuji Mizumoto, David W. Belangia, Alba Luz Zelaya Guardado, Julia Vodopiutz, Munis Dündar, Volker Straub, Arno Lingenhel, Andreas Melmer, Silvia Lechner, Johannes Zschocke, Kazuyuki Sugahara, Andreas Janecke	2013	69
11	Filaggrin Genotype in Ichthyosis Vulgaris Predicts Abnormalities in Epidermal Structure and Function American Journal Of Pathology ·Robert Gruber, Peter M. Elias, Debra Crumrine, O.V. Kruglov, Johanna M. Brandner, Jean‐Pierre Hachem, Richard B. Presland, Philip Fleckman, Andreas Janecke, Aileen Sandilands, W.H. Irwin McLean, Peter Fritsch, Michael Mildner, Erwin Tschachler, Matthias Schmuth	2011	176
12	Loss of Dermatan-4-Sulfotransferase 1 Function Results in Adducted Thumb-Clubfoot Syndrome The American Journal of Human Genetics ·Munis Dündar, Thomas Müller, Qi Zhang, Jing Pan, Beat Steinmann, Julia Vodopiutz, Robert Gruber, Tohru Sonoda, Birgit Krabichler, Gerd Utermann, Jacques Baenziger, Lijuan Zhang, Andreas Janecke	2009	110
13	Prenatal Diagnosis of Apert Syndrome with Cloverleaf Skull Deformity Using Ultrasound, Fetal Magnetic Resonance Imaging and Genetic Analysis Fetal Diagnosis and Therapy ·Benedikt Weber, Anton H. Schwabegger, Julia Vodopiutz, Andreas Janecke, Rosemarie Forstner, H. Steiner	2009	10
14	Congenital type IV glycogenosis: the spectrum of pleomorphic polyglucosan bodies in muscle, nerve, and spinal cord with two novel mutations in the GBE1 gene Acta Neuropathologica ·Kay Nolte, Andreas Janecke, Matthias Vorgerd, Joachim Weis, J. M. Schröder	2008	28
15	Van-der-Woude-Syndrom Klinische Pädiatrie ·Barbara Del Frari, Margareth Amort, Andreas Janecke, Sofia Shafi, Hildegunde Piza‐Katzer	2008	1
16	Spondylocheiro Dysplastic Form of the Ehlers-Danlos Syndrome—An Autosomal-Recessive Entity Caused by Mutations in the Zinc Transporter Gene SLC39A13 The American Journal of Human Genetics ·Cecilia Giunta, Nursel Elçioğlu, Beate Albrecht, Georg Eich, Céline Chambaz, Andreas Janecke, Heather N. Yeowell, MaryAnn Weis, David R. Eyre, Marius Kraenzlin, Beat Steinmann	2008	149
17	The Phenotypes of Patients and Heterozygous Carriers With RDH12 Mutations Are Different From Those With RPE65 Mutations Investigative Ophthalmology & Visual Science ·Brittney C. Sly, I. López, Gerald A. Fishman, Julie Racine, Allison Dorfman, Pierre Lachapelle, Andreas Janecke, F.P.M. Cremers, Rando Allikmets, Robert K. Koenekoop	2005	1
18	Evidence for genetic heterogeneity in lymphedema-cholestasis syndrome The Journal of Pediatrics ·Martin Frühwirth, Andreas Janecke, Thomas Müller, Victoria Carlton, Florian Kronenberg, Felix Offner, A. S. Knisely, Silvana Geleff, Hermela Zewge Shiferaw, Burkhard Simma, Alfred Königsrainer, Raimund Margreiter, C. B. van der Hagen, Kristin Eiklid, Øystein Aagenæs, Laura N. Bull, Helmut Ellemunter	2003	13
19	Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria Human Genetics ·Andreas Janecke, Florian Onyr Rascoussier, Barbara Günther, Barbara Utermann, Andreas Th. Müller, Judith Löffler, Gerd Utermann, Doris Nekahm-Heis	2002	62
20	Congenital sodium diarrhea is an autosomal recessive disorder of sodium/proton exchange but unrelated to known candidate genes Gastroenterology ·Thomas Müller, Cisca Wijmenga, Alan D. Phillips, Andreas Janecke, Roderick H.J. Houwen, H. A. Fischer, Helmut Ellemunter, Martin Frühwirth, Felix Offner, Sabine E. Hofer, Wilfried Müller, I W Booth, Peter Heinz‐Erian	2000	45

About Andreas Janecke

Andreas Janecke is a scholar working on Genetics, Gastroenterology, Sensory Systems, Cell Biology and Genetics, having authored 132 papers that have together received 4.4k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (10 papers), Digestive system and related health (10 papers), Celiac Disease Research and Management (9 papers), Genetics and Neurodevelopmental Disorders (9 papers), Connective tissue disorders research (8 papers), Glycogen Storage Diseases and Myoclonus (8 papers), Hearing, Cochlea, Tinnitus, Genetics (7 papers) and Genetic and Kidney Cyst Diseases (7 papers). The work is most often cited by research in Sensory Systems (309 citations), Genetics (1.3k citations), Cell Biology (694 citations), Neurology (271 citations) and Molecular Biology (2.2k citations). Andreas Janecke has collaborated with scholars based in Austria, Germany and United States. Frequent co-authors include Thomas Müller, Gerd Utermann, Andreas Gal, Robert Gruber, Lukas A. Huber, Heinz Zoller, Barbara Günther, Michael W. Hess, Georg F. Vogel and Peter Heinz‐Erian. Their work appears in journals such as Human Mutation, European Journal of Human Genetics, Journal of Pediatric Gastroenterology and Nutrition, Human Genetics and The American Journal of Human 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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