Bitten Schönewolf‐Greulich

713 total citations
18 papers, 168 citations indexed

About

Bitten Schönewolf‐Greulich is a scholar working on Genetics, Molecular Biology and Clinical Psychology. According to data from OpenAlex, Bitten Schönewolf‐Greulich has authored 18 papers receiving a total of 168 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Clinical Psychology. Recurrent topics in Bitten Schönewolf‐Greulich's work include Genetics and Neurodevelopmental Disorders (10 papers), Autism Spectrum Disorder Research (5 papers) and Family and Disability Support Research (4 papers). Bitten Schönewolf‐Greulich is often cited by papers focused on Genetics and Neurodevelopmental Disorders (10 papers), Autism Spectrum Disorder Research (5 papers) and Family and Disability Support Research (4 papers). Bitten Schönewolf‐Greulich collaborates with scholars based in Denmark, Australia and Netherlands. Bitten Schönewolf‐Greulich's co-authors include Anne‐Marie Bisgaard, Kirstine Ravn, Zeynep Tümer, Morten Dunø, Karen Brøndum‐Nielsen, Rikke S. Møller, Cathrine Jespersgaard, Lotte Risom, Flemming Wibrand and Rikke Middelhede Hansen and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Disability and Rehabilitation.

In The Last Decade

Bitten Schönewolf‐Greulich

16 papers receiving 167 citations

Peers

Countries citing papers authored by Bitten Schönewolf‐Greulich

Since Specialization

Citations

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

Fields of papers citing papers by Bitten Schönewolf‐Greulich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bitten Schönewolf‐Greulich. 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 Bitten Schönewolf‐Greulich. The network helps show where Bitten Schönewolf‐Greulich may publish in the future.

Co-authorship network of co-authors of Bitten Schönewolf‐Greulich

This figure shows the co-authorship network connecting the top 25 collaborators of Bitten Schönewolf‐Greulich. A scholar is included among the top collaborators of Bitten Schönewolf‐Greulich 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 Bitten Schönewolf‐Greulich. Bitten Schönewolf‐Greulich is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	National clinical Genetic Networks - GENets - Establishment of expert collaborations in Denmark 2023 ·European Journal of Medical Genetics ·Dorte L. Lildballe, Anja Lisbeth Frederiksen, Bitten Schönewolf‐Greulich, Charlotte Brasch‐Andersen, Charlotte Kvist Lautrup, (unknown), Inge Søkilde Pedersen, Lone Sunde, Lotte Risom, Maria Rasmussen, Mette Bertelsen, Mette Klarskov Andersen, Nanna Dahl Rendtorff, Pernille Axél Gregersen, Pernille Mathiesen Tørring, Sophia Hammer‐Hansen, Susanne E. Boonen, Suzanne Granhøj Lindquist, Trine Bjørg Hammer, Birgitte Rode Diness	0
2	Early diagnosis enabling precision medicine treatment in a young boy with PIK3R1-related overgrowth 2022 ·European Journal of Medical Genetics ·Bitten Schönewolf‐Greulich, (unknown), Tina Duelund Hjortshøj, Finn Stener Jørgensen, (unknown), (unknown), Hanne Hove, Birgitte Rode Diness	5
3	Clinical and molecular delineation of PUS3 ‐associated neurodevelopmental disorders 2021 ·Clinical Genetics ·(unknown), (unknown), Bitten Schönewolf‐Greulich, Alexandra Afenjar, Magalie Barth, Felix Boschann, Diane Doummar, Tobias B. Haack, Boris Keren, Л. А. Лившиц, Davide Mei, Joohyun Park, Tiziana Pisano, (unknown), Muhammad Umair, Ahmed Waqas, Alban Ziegler, Renzo Guerrini, Rikke S. Møller, Zeynep Tümer	26
4	Decline in gross motor skills in adult Rett syndrome; results from a Danish longitudinal study 2021 ·American Journal of Medical Genetics Part A ·Anne‐Marie Bisgaard, Kingsley Wong, (unknown), (unknown), Bitten Schönewolf‐Greulich, (unknown), Jenny Downs, (unknown)	10
5	Mutational analysis of TSC1 and TSC2 in Danish patients with tuberous sclerosis complex 2020 ·Scientific Reports ·(unknown), (unknown), (unknown), Bitten Schönewolf‐Greulich, (unknown), (unknown), Morten Dunø, Jakob Ek, Lotte Risom, Mark Nellist, Lisbeth Birk Møller	17
6	Mitochondrial Function in Gilles de la Tourette Syndrome Patients With and Without Intragenic IMMP2L Deletions 2020 ·Frontiers in Neurology ·Victoria A. Bjerregaard, Bitten Schönewolf‐Greulich, Lene Juel Rasmussen, Claus Desler, Zeynep Tümer	6
7	Mosaic MECP2 variants in males with classical Rett syndrome features, including stereotypical hand movements 2018 ·Clinical Genetics ·Bitten Schönewolf‐Greulich, Anne‐Marie Bisgaard, Morten Dunø, Cathrine Jespersgaard, (unknown), (unknown), (unknown), (unknown), Meral Topçu, Simran Kaur, Nicole J. Van Bergen, Karen Brøndum‐Nielsen, Martin J. Larsen, Kristina P. Sørensen, John Christodoulou, Christina Fagerberg, Zeynep Tümer	11
8	Development of hypomelanotic macules is associated with constitutive activated mTORC1 in tuberous sclerosis complex 2017 ·Molecular Genetics and Metabolism ·Lisbeth Birk Møller, Bitten Schönewolf‐Greulich, (unknown), (unknown), John R. Østergaard, Mette Sommerlund, (unknown), Brian Stausbøl‐Grøn, Karen Markussen Linnet, Pernille Axél Gregersen, Uffe Birk Jensen	4
9	Clinician’s guide to genes associated with Rett‐like phenotypes—Investigation of a Danish cohort and review of the literature 2017 ·Clinical Genetics ·Bitten Schönewolf‐Greulich, (unknown), Rikke S. Møller, Morten Dunø, Karen Brøndum‐Nielsen, Simranpreet Kaur, Nicole J. Van Bergen, Sebastian Lunke, Stefanie Eggers, Cathrine Jespersgaard, John Christodoulou, Zeynep Tümer	16
10	Functional abilities in aging women with Rett syndrome – the Danish cohort 2016 ·Disability and Rehabilitation ·Bitten Schönewolf‐Greulich, (unknown), (unknown), (unknown), Anne‐Marie Bisgaard	19
11	The MECP2 variant c.925C>T (p.Arg309Trp) causes intellectual disability in both males and females without classic features of Rett syndrome 2016 ·Clinical Genetics ·Bitten Schönewolf‐Greulich, María‐Isabel Tejada, (unknown), Kinga Hadzsiev, Julie Gauthier, Karen Brøndum‐Nielsen, Rolph Pfundt, Kirstine Ravn, (unknown), Blanca Gener, Cristina Martínez-Bouzas, Amélie Piton, Guy A. Rouleau, Jill Clayton‐Smith, Tjitske Kleefstra, Anne‐Marie Bisgaard, Zeynep Tümer	14
12	[Clinical molecular genetics diagnostics of Rett syndrome in Denmark]. 2015 ·PubMed ·Bitten Schönewolf‐Greulich, Morten Dunø, Kirstine Ravn, Karen Brøndum‐Nielsen, Anne‐Marie Bisgaard	1
13	Is it possible to diagnose Rett syndrome before classical symptoms become obvious? Review of 24 Danish cases born between 2003 and 2012 2015 ·European Journal of Paediatric Neurology ·Anne‐Marie Bisgaard, Bitten Schönewolf‐Greulich, Kirstine Ravn, (unknown)	12
14	Neonatal mitochondrial hepatoencephalopathy caused by novel GFM1 mutations 2015 ·SHILAP Revista de lepidopterología ·Kirstine Ravn, Bitten Schönewolf‐Greulich, Rikke Middelhede Hansen, (unknown), Morten Dunø, Flemming Wibrand, Elsebet Østergaard	13
15	P189 – 2279: Is the regression period in Rett syndrome well defined and easy to recognize? 2015 ·European Journal of Paediatric Neurology ·Anne‐Marie Bisgaard, (unknown), (unknown), (unknown), Bitten Schönewolf‐Greulich	1
16	Segregation of a 4p16.3 duplication with a characteristic appearance, macrocephaly, speech delay and mild intellectual disability in a 3‐generation family 2013 ·American Journal of Medical Genetics Part A ·Bitten Schönewolf‐Greulich, Kirstine Ravn, (unknown), Karen Brøndum‐Nielsen, Zeynep Tümer	8
17	Two new cases with microdeletion of 17q23.2 suggest presence of a candidate gene for sensorineural hearing loss within this region 2011 ·American Journal of Medical Genetics Part A ·Bitten Schönewolf‐Greulich, Anne Ronan, (unknown), (unknown), Marianne Lodahl, (unknown), Nanna Dahl Rendtorff, Lisbeth Tranebjærg, Karen Brøndum‐Nielsen, Zeynep Tümer	5
18	[Increased nuchal translucency in osteogenesis imperfecta]. 2011 ·PubMed ·Bitten Schönewolf‐Greulich, Lillian Skibsted, Lisa Leth Maroun, Allan M. Lund, Karen Brøndum‐Nielsen	0

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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