Jacqueline Schoumans

4.8k total citations
73 papers, 2.5k citations indexed

About

Jacqueline Schoumans is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jacqueline Schoumans has authored 73 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Genetics, 26 papers in Molecular Biology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jacqueline Schoumans's work include Genomic variations and chromosomal abnormalities (42 papers), Genomics and Rare Diseases (13 papers) and Genetics and Neurodevelopmental Disorders (13 papers). Jacqueline Schoumans is often cited by papers focused on Genomic variations and chromosomal abnormalities (42 papers), Genomics and Rare Diseases (13 papers) and Genetics and Neurodevelopmental Disorders (13 papers). Jacqueline Schoumans collaborates with scholars based in Sweden, Switzerland and Netherlands. Jacqueline Schoumans's co-authors include Elisabeth Blennow, Magnus Nordenskjöld, Britt‐Marie Anderlid, Ann Nordgren, Sigrid Sahlén, Nicole de Leeuw, Johan Staaf, Göran Annerén, Josephine Wincent and Britt-Marie Anderlid and has published in prestigious journals such as Nature Genetics, The Journal of Experimental Medicine and SHILAP Revista de lepidopterología.

In The Last Decade

Jacqueline Schoumans

70 papers receiving 2.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jacqueline Schoumans Sweden 29 1.6k 1.2k 458 442 238 73 2.5k
Hutton M. Kearney United States 21 2.2k 1.4× 1.1k 1.0× 196 0.4× 1.0k 2.4× 174 0.7× 40 3.2k
Palma Finelli Italy 29 1.0k 0.7× 1.2k 1.1× 466 1.0× 211 0.5× 105 0.4× 95 2.2k
Svetlana A. Yatsenko United States 26 1.8k 1.2× 1.5k 1.3× 366 0.8× 628 1.4× 130 0.5× 110 3.0k
Lester Weiss United States 29 1.4k 0.9× 918 0.8× 416 0.9× 448 1.0× 184 0.8× 82 2.3k
Umadevi Tantravahi United States 29 946 0.6× 1.4k 1.2× 281 0.6× 416 0.9× 124 0.5× 67 2.7k
Jayne Y. Hehir‐Kwa Netherlands 24 1.1k 0.7× 854 0.7× 221 0.5× 378 0.9× 68 0.3× 53 1.9k
B S Emanuel United States 30 1.1k 0.7× 1.8k 1.5× 346 0.8× 257 0.6× 459 1.9× 44 2.9k
Dvorah Abeliovich Israel 31 1.4k 0.9× 1.5k 1.3× 141 0.3× 450 1.0× 158 0.7× 98 3.0k
Blake C. Ballif United States 36 3.2k 2.0× 1.8k 1.5× 776 1.7× 1.3k 3.0× 234 1.0× 75 4.0k
Udo Trautmann Germany 23 1.1k 0.7× 930 0.8× 331 0.7× 328 0.7× 97 0.4× 65 1.7k

Countries citing papers authored by Jacqueline Schoumans

Since Specialization
Citations

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

Fields of papers citing papers by Jacqueline Schoumans

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacqueline Schoumans

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

All Works

20 of 20 papers shown
1.
Parker, Helen, et al.. (2026). Exploring the synergy between telomere length and genomic complexity in CLL. British Journal of Haematology. 208(3). 1121–1126.
2.
3.
Hoffmann, Michèle J., Yara Banz, Jörg Halter, et al.. (2024). True Donor Cell Leukemia after Allogeneic Hematopoietic Stem Cell Transplantation: Diagnostic and Therapeutic Considerations—Brief Report. Current Oncology. 31(4). 2067–2075.
4.
Papadopoulou, Vasiliki, et al.. (2023). Single-center, observational study of AML/MDS-EB with IDH1/2 mutations: genetic profile, immunophenotypes, mutational kinetics and outcomes. Hematology. 28(1). 2180704–2180704. 3 indexed citations
5.
Flach, Johanna, Evgenii Shumilov, Naomi Porret, et al.. (2019). Detection of rare reciprocal RUNX1 rearrangements by next‐generation sequencing in acute myeloid leukemia. Genes Chromosomes and Cancer. 59(4). 268–274. 7 indexed citations
6.
L’Abbate, Alberto, Doron Tolomeo, Angelo Lonoce, et al.. (2015). t(15;21) translocations leading to the concurrent downregulation of RUNX1 and its transcription factor partner genes SIN3A and TCF12 in myeloid disorders. Molecular Cancer. 14(1). 211–211. 14 indexed citations
7.
Wehner, Peter, Lennart Opitz, Gabriela Salinas-Riester, et al.. (2014). CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance. Human Genetics. 133(8). 997–1009. 88 indexed citations
8.
Du, Likun, Torkild Visnes, Andrea Björkman, et al.. (2013). A regulatory role for the cohesin loader NIPBL in nonhomologous end joining during immunoglobulin class switch recombination. The Journal of Experimental Medicine. 210(12). 2503–2513. 29 indexed citations
9.
Simons, Annet, et al.. (2012). Genome-wide arrays in routine diagnostics of hematological malignancies. Human Mutation. 33(6). 941–948. 44 indexed citations
10.
Gijsbers, A.C.J., Jacqueline Schoumans, & Claudia Ruivenkamp. (2011). Interpretation of Array Comparative Genome Hybridization Data: A Major Challenge. Cytogenetic and Genome Research. 135(3-4). 222–227. 29 indexed citations
11.
Lundin, Johanna, Cilla Söderhäll, Anna Hammarsjö, et al.. (2010). 22q11.2 microduplication in two patients with bladder exstrophy and hearing impairment. European Journal of Medical Genetics. 53(2). 61–65. 32 indexed citations
12.
Schoumans, Jacqueline & Claudia Ruivenkamp. (2010). Laboratory Methods for the Detection of Chromosomal Abnormalities. Methods in molecular biology. 628. 53–73. 2 indexed citations
13.
Wincent, Josephine, et al.. (2010). High-resolution molecular karyotyping in patients with developmental delay and/or multiple congenital anomalies in a clinical setting. Clinical Genetics. 79(2). 147–157. 24 indexed citations
14.
Lindstrand, Anna, H Malmgren, Sigrid Sahlén, et al.. (2009). Detailed molecular and clinical characterization of three patients with 21q deletions. Clinical Genetics. 77(2). 145–154. 52 indexed citations
15.
Soysal, Yasemin, Sevim Balcı, Thomas Liehr, et al.. (2009). Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy. American Journal of Medical Genetics Part A. 149A(12). 2782–2787. 13 indexed citations
16.
Fossum, Magdalena, et al.. (2005). Long-Term Culture of Human Urothelial Cells – A Qualitative Analysis. Cells Tissues Organs. 181(1). 11–22. 13 indexed citations
17.
Schoumans, Jacqueline, Johan Staaf, Göran Jönsson, et al.. (2005). Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith–Magenis syndrome minimum deletion to ~650 kb. European Journal of Medical Genetics. 48(3). 290–300. 11 indexed citations
18.
Schoumans, Jacqueline, Ann Nordgren, Claudia Ruivenkamp, et al.. (2004). Genome-wide screening using array-CGH does not reveal microdeletions/microduplications in children with Kabuki syndrome. European Journal of Human Genetics. 13(2). 260–263. 23 indexed citations
19.
Ciccarelli, A., H. Valdes‐Socin, Jasmine Parma, et al.. (2004). Thyrotoxic adenoma followed by atypical hyperthyroidism due to struma ovarii: clinical and genetic studies. European Journal of Endocrinology. 150(4). 431–437. 21 indexed citations
20.
Chen, Jindong, Weng‐Onn Lui, Michele D. Vos, et al.. (2003). The t(1;3) breakpoint-spanning genes LSAMP and NORE1 are involved in clear cell renal cell carcinomas. Cancer Cell. 4(5). 405–413. 89 indexed citations

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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