Bianca M. de Graaf

2.0k citations

15 papers · 458 indexed · h-index 9

Co-authors: Ben A. Oostra Peter Heutink Esther Brusse Dennis Dooijes Elmar Krieger Inge de Koning Peter A. J. Leegwater Raoul van de Graaf
Topics: Congenital gastrointestinal and neural anomalies (6 papers)Congenital heart defects research (5 papers)Digestive system and related health (3 papers)
Cited by: Urology Cellular and Molecular Neuroscience Molecular Biology
Journals: Gastroenterology International Journal of Molecular Sciences Journal of the American Society of Nephrology
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Bianca M. de Graaf

15 papers receiving 452 citations

Peers

Countries citing papers authored by Bianca M. de Graaf

Since Specialization

Citations

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

Fields of papers citing papers by Bianca M. de Graaf

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bianca M. de Graaf. 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 Bianca M. de Graaf. The network helps show where Bianca M. de Graaf may publish in the future.

Co-authorship network of co-authors of Bianca M. de Graaf

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	ATP5PO levels regulate enteric nervous system development in zebrafish, linking Hirschsprung disease to Down Syndrome 2023 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Laura E. Kuil,Rajeev Kumar Chauhan,Bianca M. de Graaf,(unknown),(unknown),(unknown),Catherine Verhaeghe,(unknown),David C. Schriemer,(unknown),Alice S. Brooks,Sarah Edie,Roger H. Reeves,Bart J. L. Eggen,Iain T. Shepherd,Alan J. Burns,Robert M.W. Hofstra,Veerle Melotte,Erwin Brosens,Maria M. Alves	2
2	The long Filamin-A isoform is required for intestinal development and motility: implications for chronic intestinal pseudo-obstruction 2022 ·Human Molecular Genetics ·(unknown),Yuying Zhao,Danny Halim,(unknown),Herma C. van der Linde,(unknown),(unknown),Bianca M. de Graaf,Robert M. Verdijk,Alice S. Brooks,Iain T. Shepherd,Ya Gao,Alan J. Burns,Robert M.W. Hofstra,Maria M. Alves	8
3	TFAP2B Haploinsufficiency Impacts Gastrointestinal Function and Leads to Pediatric Intestinal Pseudo-obstruction 2022 ·Frontiers in Cell and Developmental Biology ·(unknown),Laura E. Kuil,Bianca M. de Graaf,(unknown),(unknown),Alice S. Brooks,Marjon van Slegtenhorst,Barbara de Koning,René Wijnen,Veerle Melotte,Robert M.W. Hofstra,Erwin Brosens,Maria M. Alves	8
4	Intrinsic Cellular Susceptibility to Barrett’s Esophagus in Adults Born with Esophageal Atresia 2022 ·Cancers ·(unknown),Annelies de Klein,Bianca M. de Graaf,Michail Doukas,Antti Koivusalo,Mikko P. Pakarinen,(unknown),(unknown),Hanneke IJsselstijn,Yolande van Bever,René Wijnen,Manon C.W. Spaander,Erwin Brosens	2
5	The Somatic Mutation Paradigm in Congenital Malformations: Hirschsprung Disease as a Model 2021 ·International Journal of Molecular Sciences ·(unknown),(unknown),Rajendra Chauhan,Yunia Sribudiani,Bianca M. de Graaf,(unknown),Rutger W. W. Brouwer,Wilfred F. J. van IJcken,Ivo de Blaauw,Alice S. Brooks,Cornelius E. J. Sloots,(unknown),René Wijnen,Donald F. Newgreen,Alan J. Burns,Robert M.W. Hofstra,Maria M. Alves,Erwin Brosens	2
6	Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung Disease 2018 ·Gastroenterology ·Yunia Sribudiani,Rajendra Chauhan,Maria M. Alves,(unknown),Erwin Brosens,(unknown),(unknown),Bianca M. de Graaf,(unknown),Grzegorz Burzynski,Rutger W. W. Brouwer,Wilfred F. J. van IJcken,Saskia M. Maas,Annelies de Klein,Jan Osinga,Bart J. L. Eggen,Alan J. Burns,Alice S. Brooks,Iain T. Shepherd,Robert M.W. Hofstra	26
7	Loss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis Syndrome 2017 ·The American Journal of Human Genetics ·Danny Halim,Erwin Brosens,Françoise Müller,Michael F. Wangler,Arthur L. Beaudet,James R. Lupski,Zeynep H. Coban Akdemir,Michael Doukas,Hans Stoop,Bianca M. de Graaf,Rutger W. W. Brouwer,Wilfred F. J. van IJcken,Jean‐François Oury,Jonathan Rosenblatt,Alan J. Burns,Dick Tibboel,Robert M.W. Hofstra,Maria M. Alves	52
8	Genetic screening of Congenital Short Bowel Syndrome patients confirms CLMP as the major gene involved in the recessive form of this disorder 2016 ·European Journal of Human Genetics ·Maria M. Alves,Danny Halim,Reza Maroofian,Bianca M. de Graaf,Raoul Rooman,(unknown),Els Van de Vijver,(unknown),(unknown),Barry A. Chioza,Emma L. Baple,Mohammadreza Dehghani,Andrew H. Crosby,Robert M.W. Hofstra	17
9	RET and EDNRB mutation screening in patients with Hirschsprung disease: Functional studies and its implications for genetic counseling 2015 ·European Journal of Human Genetics ·(unknown),Shamiram Melhem,(unknown),Bianca M. de Graaf,Richard J. Sinke,(unknown),(unknown),Ahmad Hamim Sadewa,(unknown),Yati Soenarto,Robert M.W. Hofstra,Yunia Sribudiani	14
10	Autosomal dominant inheritance of cardiac valves anomalies in two families: Extended spectrum of left‐ventricular outflow tract obstruction 2009 ·American Journal of Medical Genetics Part A ·Marja W. Wessels,Ingrid M.B.H. van de Laar,Jolien W. Roos‐Hesselink,Sipke Strikwerda,Daniëlle Majoor‐Krakauer,Bert B.A. de Vries,Wilhelmina S. Kerstjens‐Frederikse,Yvonne J. Vos,Bianca M. de Graaf,Aida M. Bertoli‐Avella,Patrick J. Willems	4
11	A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier? 2009 ·Neurogenetics ·Esther Brusse,Daniëlle Majoor‐Krakauer,Bianca M. de Graaf,Gerhard H. Visser,Sigrid M. A. Swagemakers,Agnita J.W. Boon,Ben A. Oostra,Aida M. Bertoli‐Avella	12
12	ROBO2 Gene Variants Are Associated with Familial Vesicoureteral Reflux 2008 ·Journal of the American Society of Nephrology ·Aida M. Bertoli‐Avella,(unknown),Francesca Punzo,Bianca M. de Graaf,Giuliana Lama,Angela La Manna,Cesare Polito,Carolina Grassia,Brúno Nobili,Pier Francesco Rambaldi,Ben A. Oostra,Silverio Perrotta	55
13	A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity 2008 ·Pediatric Nephrology ·(unknown),Aida M. Bertoli‐Avella,Bianca M. de Graaf,Francesca Punzo,Giuliana Lama,Angela La Manna,Carolina Grassia,Pier Francesco Rambaldi,Ben A. Oostra,Silverio Perrotta	25
14	A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p 2007 ·Human Genetics ·Marja W. Wessels,Bianca M. de Graaf,Titia E. Cohen‐Overbeek,Silja E.C. Spitaels,Lotte E. de Groot–de Laat,Folkert J. ten Cate,(unknown),Ronald R. de Krijger,Margot M. Bartelings,(unknown),J. W. Wladimiroff,Martinus F. Niermeijer,Peter Heutink,Ben A. Oostra,Dennis Dooijes,Aida M. Bertoli‐Avella,Patrick J. Willems	26
15	A Mutation in the Fibroblast Growth Factor 14 Gene Is Associated with Autosomal Dominant Cerebral Ataxia 2003 ·The American Journal of Human Genetics ·John C. van Swieten,Esther Brusse,Bianca M. de Graaf,Elmar Krieger,Raoul van de Graaf,Inge de Koning,Anneke Maat‐Kievit,Peter A. J. Leegwater,Dennis Dooijes,Ben A. Oostra,Peter Heutink	205

About Bianca M. de Graaf

Bianca M. de Graaf is a scholar working on Gastroenterology, Nutrition and Dietetics and Genetics, having authored 15 papers that have together received 458 indexed citations. Recurring topics across this work include Congenital gastrointestinal and neural anomalies (6 papers), Congenital heart defects research (5 papers) and Digestive system and related health (3 papers). The work is most often cited by research in Urology (55 citations), Cellular and Molecular Neuroscience (135 citations) and Molecular Biology (301 citations). Bianca M. de Graaf has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Ben A. Oostra, Peter Heutink, Esther Brusse, Dennis Dooijes, Elmar Krieger, Inge de Koning, Peter A. J. Leegwater, Raoul van de Graaf, John C. van Swieten and Anneke Maat‐Kievit. Their work appears in journals such as Gastroenterology, International Journal of Molecular Sciences and Journal of the American Society of Nephrology.

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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