J. J. P. Schrander

718 citations

21 papers · 527 indexed · h-index 10

Co-authors: C. T. R. M. Schrander‐Stumpel P. P. Forget R. H. Kuijten Arnold D.M. Kester J.J.M. Engelen J. P. Fryns Patricia Forget Peter Meinecke
Topics: Genetic Syndromes and Imprinting (5 papers)Genomic variations and chromosomal abnormalities (5 papers)Neurogenetic and Muscular Disorders Research (4 papers)
Cited by: Immunology and Allergy Pharmacy Gastroenterology
Journals: British Journal of Dermatology Allergy Journal of Medical Genetics
Partner nations: Netherlands United States Belgium

In The Last Decade

J. J. P. Schrander

21 papers receiving 500 citations

Peers

Countries citing papers authored by J. J. P. Schrander

Since Specialization

Citations

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

Fields of papers citing papers by J. J. P. Schrander

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J. J. P. Schrander. 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 J. J. P. Schrander. The network helps show where J. J. P. Schrander may publish in the future.

Co-authorship network of co-authors of J. J. P. Schrander

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Adducted thumbs: A clinical clue to genetic diagnosis 2012 ·European Journal of Medical Genetics ·Judith M.A. Verhagen,C. T. R. M. Schrander‐Stumpel,(unknown),Jacobiene W. Weber,J. J. P. Schrander,M. Estela Rubio‐Gozalbo,Jaap Bakker,Alexander P.A. Stegmann,Yvonne J. Vos,Suzanna G.M. Frints	9
2	Ehlers–Danlos arthrochalasia type (VIIA–B) – expanding the phenotype: from prenatal life through adulthood 2011 ·Clinical Genetics ·Merel Klaassens,Eyal Reinstein,Yvonne Hilhorst‐Hofstee,J. J. P. Schrander,Fransiska Malfait,(unknown),(unknown),(unknown),(unknown),Deborah Krakow,Anne De Paepe,Maurice A. M. Van Steensel,Gerard Pals,(unknown),(unknown)	26
3	Unique skin changes in a case of Albright hereditary osteodystrophy caused by a rare GNAS1 mutation 2009 ·British Journal of Dermatology ·Merel Klaassens,Eveline W Blom,J. J. P. Schrander,Carrie Ris‐Stalpers,A. C. Nieuwenhuijzen Kruseman,Maurice A. M. Van Steensel,C. T. R. M. Schrander‐Stumpel	6
4	A patient with a de novo 15q24q26.1 interstitial deletion, developmental delay, mild dysmorphism, and very blue irises 2004 ·American Journal of Medical Genetics Part A ·Liesbeth Spruijt,J.J.M. Engelen,(unknown),(unknown),J. J. P. Schrander,C. T. R. M. Schrander‐Stumpel	7
5	Determinants of neonatal IgE level: parity, maternal age, birth season and perinatal essential fatty acid status in infants of atopic mothers 2004 ·Allergy ·(unknown),Carel Thijs,Pieter C. Dagnelie,C. J. M. Henquet,A.C. van Houwelingen,J. J. P. Schrander,P. P. C. A. Menheere,(unknown)	34
6	Trisomy 7p: report of 2 patients and literature review. 2000 ·PubMed ·Yvonne Arens,Annick Toutain,J.J.M. Engelen,J. Offermans,A.J.H. Hamers,J. J. P. Schrander,(unknown),Connie Schrander‐Stumpel	14
7	Two sibs with an unusual pattern of skeletal malformations resembling osteogenesis imperfecta: a new type of skeletal dysplasia? 1999 ·Journal of Medical Genetics ·Ute Moog,P Maroteaux,C. T. R. M. Schrander‐Stumpel,(unknown),J. J. P. Schrander,(unknown)	4
8	Phenotypic overlap between McKusick-Kaufman and Bardet-Biedl syndromes: are they related? 1998 ·PubMed ·C. Schaap,M.P.M. ten Tusscher,J. J. P. Schrander,R. H. Kuijten,C. T. R. M. Schrander‐Stumpel	9
9	Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletion 1997 ·European Journal of Pediatrics ·Kate Chandler,Christine de Die‐Smulders,J.J.M. Engelen,J. J. P. Schrander	15
10	Does food intolerance play a role in juvenile chronic arthritis? 1997 ·Lara D. Veeken ·J. J. P. Schrander,Carlo Marcelis,Marcel P. de Vries,(unknown)	8
11	Deletion of the long arm of chromosome 6: two new patients and literature review 1996 ·Clinical Genetics ·L. J. M. Evers,C. T. R. M. Schrander‐Stumpel,J.J.M. Engelen,(unknown),(unknown),J. J. P. Schrander,(unknown),J. Peters,J. P. Fryns	21
12	Cerebro-costo-mandibular syndrome: a follow-up study with 6 patients. 1996 ·PubMed ·C. T. R. M. Schrander‐Stumpel,(unknown),(unknown),Peter Meinecke,E Rupprecht,P Maroteaux,J. J. P. Schrander,Jean‐Pierre Fryns	3
13	The Kabuki make-up (Niikawa-Kuroki) syndrome: 12 new patients, further delineation of the non-Japanese phenotype 1994 ·C. T. R. M. Schrander‐Stumpel,Peter Meinecke,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Eric Legius,J. J. P. Schrander,(unknown)	4
14	The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patients 1994 ·European Journal of Pediatrics ·C. T. R. M. Schrander‐Stumpel,Peter Meinecke,Golder N. Wilson,(unknown),Sigrid Tinschert,Rainer König,N. Philip,Renata Rizzo,J. J. P. Schrander,(unknown),Anneke Maat‐Kievit,I. van der Bürgt,(unknown),(unknown),(unknown),Alain Verloès,Hubert Journel,J P Fryns	88
15	The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patients 1994 ·European Journal of Pediatrics ·(unknown),Peter Meinecke,Golder N. Wilson,Gabriele Gillessen‐Kaesbach,Sigrid Tinschert,(unknown),N. Philip,(unknown),J. J. P. Schrander,(unknown),(unknown),I. van der Bürgt,(unknown),(unknown),(unknown),Alain Verloès,Hubert Journel,(unknown)	5
16	Small intestinal mucosa IgE plasma cells and specific anti-cow milk IgE in children with cow milk protein intolerance. 1993 ·PubMed ·J. J. P. Schrander,(unknown),Jan‐Willem Arends,P. P. Forget,R. H. Kuijten	5
17	Cow's milk protein intolerance in infants under 1 year of age: A prospective epidemiological study 1993 ·European Journal of Pediatrics ·J. J. P. Schrander,(unknown),P. P. Forget,C. T. R. M. Schrander‐Stumpel,R. H. Kuijten,Arnold D.M. Kester	181
18	Follow up study of cow's milk protein intolerant infants 1992 ·European Journal of Pediatrics ·J. J. P. Schrander,(unknown),Patricia Forget,R. H. Kuijten	27
19	Trisomy 17p due to a t(8; 17) (p23; p11.2)pat translocation. Case report and review of the literature 1990 ·Clinical Genetics ·C. T. R. M. Schrander‐Stumpel,J. J. P. Schrander,J. P. Fryns,Guus Hamers	20
20	[51Cr]EDTA Intestinal Permeability in Children with Cowʼs Milk Intolerance 1990 ·Journal of Pediatric Gastroenterology and Nutrition ·J. J. P. Schrander,(unknown),P. P. Forget,(unknown)	39

About J. J. P. Schrander

J. J. P. Schrander is a scholar working on Pharmacy, Genetics and Immunology and Allergy, having authored 21 papers that have together received 527 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Neurogenetic and Muscular Disorders Research (4 papers). The work is most often cited by research in Immunology and Allergy (214 citations), Pharmacy (67 citations) and Gastroenterology (50 citations). J. J. P. Schrander has collaborated with scholars based in Netherlands, United States and Belgium. Frequent co-authors include C. T. R. M. Schrander‐Stumpel, P. P. Forget, R. H. Kuijten, Arnold D.M. Kester, J.J.M. Engelen, J. P. Fryns, Patricia Forget, Peter Meinecke, Golder N. Wilson and J P Fryns. Their work appears in journals such as British Journal of Dermatology, Allergy and Journal of Medical 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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