Bianca M. de Graaf

2.0k citations

15 papers · 458 indexed · h-index 9

Urology top 10%
Cellular and Molecular Neuroscience top 10%
Molecular Biology
- Congenital heart defects research 5
Pediatrics, Perinatology and Child Health
Genetics
- Digestive system and related health 3
- Neurogenetic and Muscular Disorders Research 2
Surgery
- Congenital gastrointestinal and neural anomalies 6
- Intestinal Malrotation and Obstruction Disorders 2
Nutrition and Dietetics
- Infant Nutrition and Health 2
Gastroenterology
- Gastroesophageal reflux and treatments 1
Neurology
- Neurological diseases and metabolism 1

Co-authors: Ben A. Oostra Peter Heutink Esther Brusse Dennis Dooijes Elmar Krieger Inge de Koning Peter A. J. Leegwater Raoul van de Graaf
Cited by: Urology Cellular and Molecular Neuroscience Molecular Biology
Journals: Gastroenterology (1 paper)International Journal of Molecular Sciences (1 paper)Journal of the American Society of Nephrology (1 paper)
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

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

All Works

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15 of 15 papers shown

#	Work
1	ATP5PO levels regulate enteric nervous system development in zebrafish, linking Hirschsprung disease to Down Syndrome Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Laura E. Kuil,Rajeev Kumar Chauhan,Bianca M. de Graaf,W.W. Cheng,Naomi Kakiailatu,R. Lasabuda,Catherine Verhaeghe,Jonathan D. Windster,David C. Schriemer,Zakia Azmani,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	2023	2
2	The long Filamin-A isoform is required for intestinal development and motility: implications for chronic intestinal pseudo-obstruction Human Molecular Genetics ·Almira Zada,Yuying Zhao,Danny Halim,Jonathan D. Windster,Herma C. van der Linde,Jackleen Glodener,Sander Overkleeft,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	2022	8
3	TFAP2B Haploinsufficiency Impacts Gastrointestinal Function and Leads to Pediatric Intestinal Pseudo-obstruction Frontiers in Cell and Developmental Biology ·Almira Zada,Laura E. Kuil,Bianca M. de Graaf,Naomi Kakiailatu,Jonathan D. Windster,Alice S. Brooks,Marjon van Slegtenhorst,Barbara de Koning,René Wijnen,Veerle Melotte,Robert M.W. Hofstra,Erwin Brosens,Maria M. Alves	2022	8
4	Intrinsic Cellular Susceptibility to Barrett’s Esophagus in Adults Born with Esophageal Atresia Cancers ·Chantal A. ten Kate,Annelies de Klein,Bianca M. de Graaf,Michail Doukas,Antti Koivusalo,Mikko P. Pakarinen,Robert van der Helm,Tom Brands,Hanneke IJsselstijn,Yolande van Bever,René Wijnen,Manon C.W. Spaander,Erwin Brosens	2022	2
5	The Somatic Mutation Paradigm in Congenital Malformations: Hirschsprung Disease as a Model International Journal of Molecular Sciences ·Katherine C. MacKenzie,Rhiana Garritsen,Rajendra Chauhan,Yunia Sribudiani,Bianca M. de Graaf,Tim Rügenbrink,Rutger W. W. Brouwer,Wilfred F. J. van IJcken,Ivo de Blaauw,Alice S. Brooks,Cornelius E. J. Sloots,Conny J. H. M. Meeuwsen,René Wijnen,Donald F. Newgreen,Alan J. Burns,Robert M.W. Hofstra,Maria M. Alves,Erwin Brosens	2021	2
6	Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung Disease Gastroenterology ·Yunia Sribudiani,Rajendra Chauhan,Maria M. Alves,Lucy Petrova,Erwin Brosens,Colin Harrison,Tara D. Wabbersen,Bianca M. de Graaf,Tim Rügenbrink,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	2018	26
7	Loss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis Syndrome 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	2017	52
8	Genetic screening of Congenital Short Bowel Syndrome patients confirms CLMP as the major gene involved in the recessive form of this disorder European Journal of Human Genetics ·Maria M. Alves,Danny Halim,Reza Maroofian,Bianca M. de Graaf,Raoul Rooman,Christine S. van der Werf,Els Van de Vijver,Mohammad YV Mehrjardi,Majid Aflatoonian,Barry A. Chioza,Emma L. Baple,Mohammadreza Dehghani,Andrew H. Crosby,Robert M.W. Hofstra	2016	17
9	RET and EDNRB mutation screening in patients with Hirschsprung disease: Functional studies and its implications for genetic counseling European Journal of Human Genetics ·Titis Widowati,Shamiram Melhem,Suryono Yudha Patria,Bianca M. de Graaf,Richard J. Sinke,Martijn Viel,Jos Dijkhuis,Ahmad Hamim Sadewa,Rochadi Purwohardjono,Yati Soenarto,Robert M.W. Hofstra,Yunia Sribudiani	2015	14
10	Autosomal dominant inheritance of cardiac valves anomalies in two families: Extended spectrum of left‐ventricular outflow tract obstruction 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	2009	4
11	A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier? 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	2009	12
12	ROBO2 Gene Variants Are Associated with Familial Vesicoureteral Reflux Journal of the American Society of Nephrology ·Aida M. Bertoli‐Avella,Maria Luisa Conte,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	2008	55
13	A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity Pediatric Nephrology ·Maria Luisa Conte,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	2008	25
14	A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p 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,Ingrid Frohn‐Mulder,Ronald R. de Krijger,Margot M. Bartelings,Nienke Essed,J. W. Wladimiroff,Martinus F. Niermeijer,Peter Heutink,Ben A. Oostra,Dennis Dooijes,Aida M. Bertoli‐Avella,Patrick J. Willems	2007	26
15	A Mutation in the Fibroblast Growth Factor 14 Gene Is Associated with Autosomal Dominant Cerebral Ataxia 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	2003	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), Digestive system and related health (3 papers), Neurogenetic and Muscular Disorders Research (2 papers), Infant Nutrition and Health (2 papers), Intestinal Malrotation and Obstruction Disorders (2 papers), Gastroesophageal reflux and treatments (1 paper) and Neurological diseases and metabolism (1 paper). 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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