Birgitta Bernhard

1.8k total citations
10 papers, 114 citations indexed

About

Birgitta Bernhard is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Birgitta Bernhard has authored 10 papers receiving a total of 114 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Birgitta Bernhard's work include BRCA gene mutations in cancer (2 papers), Prenatal Screening and Diagnostics (2 papers) and Congenital heart defects research (2 papers). Birgitta Bernhard is often cited by papers focused on BRCA gene mutations in cancer (2 papers), Prenatal Screening and Diagnostics (2 papers) and Congenital heart defects research (2 papers). Birgitta Bernhard collaborates with scholars based in United Kingdom, United States and Canada. Birgitta Bernhard's co-authors include Wayne Lam, Susan Holloway, Harry Campbell, Louise C. Wilson, Saskia M. Maas, R. Frank Kooy, David Fitzpatrick, Erik Schoenmakers, Roseanne Cetnarskyj and Liesbeth Rooms and has published in prestigious journals such as Clinical Endocrinology, Human Mutation and European Journal of Human Genetics.

In The Last Decade

Birgitta Bernhard

10 papers receiving 114 citations

Peers

Countries citing papers authored by Birgitta Bernhard

Since Specialization

Citations

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

Fields of papers citing papers by Birgitta Bernhard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Birgitta Bernhard

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	A patient with a germline SDHB mutation presenting with an isolated pituitary macroprolactinoma 2018 ·Endocrinology Diabetes and Metabolism Case Reports ·Michelle Maher, Federico Roncaroli, Nigel Mendoza, Karim Meeran, Natalie Canham, (unknown), Birgitta Bernhard, David Collier, Juliana Drummond, Kassiani Skordilis, Nicola Tufton, (unknown), Niamh Martin, Márta Korbonits, Florian Wernig	9
2	Variable developmental delays and characteristic facial features—A novel 7p22.3p22.2 microdeletion syndrome? 2017 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Ingrid Cristian, Sue Price, Birgitta Bernhard, (unknown), Sunita Venkateswaran, Jean McGowan‐Jordan, Christine M. Armour	9
3	Molecular spectrum of TSHβ subunit gene defects in central hypothyroidism in the UK and Ireland 2016 ·Clinical Endocrinology ·Adeline K. Nicholas, (unknown), (unknown), Erik Schoenmakers, Mehul Dattani, (unknown), Birgitta Bernhard, Jeremy Kirk, Edna Roche, Krishna Chatterjee, Nadia Schoenmakers	21
4	Knowledge-Based Extraction of Measurement-Entity Relations from German Radiology Reports 2014 ·OPUS (Augsburg University) ·(unknown), (unknown), (unknown), Birgitta Bernhard, (unknown)	1
5	A CGG-Repeat Expansion Mutation inZNF713Causes FRA7A: Association with Autistic Spectrum Disorder in two Families 2014 ·Human Mutation ·(unknown), Jacqueline K. Rainger, (unknown), Birgitta Bernhard, Liesbeth Rooms, Daria Grafodatskaya, Rosanna Weksberg, Éric Fombonne, Martin S. Taylor, Stephen W. Scherer, R. Frank Kooy, David Fitzpatrick	27
6	ELECTRIC DRIVES FOR COMBINE HARVESTERS 2013 ·Birgitta Bernhard, (unknown)	2
7	899 DOCETAXEL RECHALLENGE VERSUS DOCETAXEL/BEVACIZUMAB IN CASTRATION-RESISTANT PROSTATE CANCER FOLLOWING FIRST LINE DOCETAXEL 2010 ·European Urology Supplements ·Axel Heidenreich, D. Thüer, David Pfister, Birgitta Bernhard	3
8	Inequality of use of Cancer Genetics Services by members of breast, ovarian and colorectal cancer families in South East Scotland 2008 ·Familial Cancer ·Susan Holloway, Birgitta Bernhard, Harry Campbell, Roseanne Cetnarskyj, Wayne Lam	8
9	Uptake of testing for BRCA1/2 mutations in South East Scotland 2008 ·European Journal of Human Genetics ·Susan Holloway, Birgitta Bernhard, Harry Campbell, Wayne Lam	16
10	Patched mutations and hairy skin patches: A new sign in Gorlin syndrome 2006 ·American Journal of Medical Genetics Part A ·Louise C. Wilson, (unknown), Birgitta Bernhard, Saskia M. Maas	18

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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