Jacqueline Siegel‐Bartelt

1.4k total citations · 1 hit paper
10 papers, 1.1k citations indexed

About

Jacqueline Siegel‐Bartelt is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Jacqueline Siegel‐Bartelt has authored 10 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Jacqueline Siegel‐Bartelt's work include Dermatological and Skeletal Disorders (2 papers), Hedgehog Signaling Pathway Studies (2 papers) and Craniofacial Disorders and Treatments (2 papers). Jacqueline Siegel‐Bartelt is often cited by papers focused on Dermatological and Skeletal Disorders (2 papers), Hedgehog Signaling Pathway Studies (2 papers) and Craniofacial Disorders and Treatments (2 papers). Jacqueline Siegel‐Bartelt collaborates with scholars based in Canada, United States and France. Jacqueline Siegel‐Bartelt's co-authors include Nancy J. Leysens, Kent W. Small, Nicole A. Datson, Pierre Bitoun, Bernhard Zabel, Wallace L.M. Alward, Elena V. Semina, Rebecca S. Reiter, J.C. Murray and John C. Carey and has published in prestigious journals such as Nature Genetics, Human Genetics and American Journal of Medical Genetics.

In The Last Decade

Jacqueline Siegel‐Bartelt

10 papers receiving 1.1k citations

Hit Papers

Cloning and characterization of a novel bicoid-related ho... 1996 2026 2006 2016 1996 200 400 600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
    1996 720 citations Elena V. Semina, Rebecca S. Reiter et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jacqueline Siegel‐Bartelt Canada 8 820 477 111 95 89 10 1.1k
Nancy J. Leysens United States 8 897 1.1× 708 1.5× 121 1.1× 94 1.0× 120 1.3× 13 1.3k
Pierre Bitoun France 17 1.4k 1.7× 818 1.7× 239 2.2× 167 1.8× 137 1.5× 39 1.9k
C. Pressman United States 7 533 0.7× 196 0.4× 54 0.5× 62 0.7× 40 0.4× 7 680
Stuart W. Tompson United States 12 482 0.6× 429 0.9× 65 0.6× 40 0.4× 34 0.4× 16 716
Abdulrahman Alswaid Saudi Arabia 16 509 0.6× 698 1.5× 74 0.7× 35 0.4× 54 0.6× 29 1.1k
Anthony J. Vivian United Kingdom 17 401 0.5× 453 0.9× 346 3.1× 203 2.1× 322 3.6× 38 1.3k
C McKeown United Kingdom 13 735 0.9× 551 1.2× 23 0.2× 58 0.6× 168 1.9× 25 1.3k
Valerie Greger Germany 18 830 1.0× 498 1.0× 224 2.0× 47 0.5× 51 0.6× 26 1.2k
Michael S. Rutenberg United States 16 530 0.6× 187 0.4× 28 0.3× 127 1.3× 95 1.1× 54 1.2k
H. Allen Gardner Canada 14 456 0.6× 193 0.4× 65 0.6× 33 0.3× 83 0.9× 32 745

Countries citing papers authored by Jacqueline Siegel‐Bartelt

Since Specialization
Citations

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

Fields of papers citing papers by Jacqueline Siegel‐Bartelt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacqueline Siegel‐Bartelt

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

All Works

10 of 10 papers shown
1.
Arnold, Paul, Jacqueline Siegel‐Bartelt, Cheryl Cytrynbaum, Ikuko Teshima, & Russell Schachar. (2001). Velo‐cardio‐facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders. American Journal of Medical Genetics. 105(4). 354–362. 75 indexed citations
2.
Carção, Manuel, Susan Blasér, Ronald Grant, Rosanna Weksberg, & Jacqueline Siegel‐Bartelt. (1998). MRI findings in macrocephaly-cutis marmorata telangiectatica congenita. American Journal of Medical Genetics. 76(2). 165–167. 29 indexed citations
3.
Chun, Kathy, Jacqueline Siegel‐Bartelt, David Chitayat, John H. Phillips, & Peter N. Ray. (1998). FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndrome. American Journal of Medical Genetics. 77(3). 219–224. 81 indexed citations
4.
Carção, Manuel, Susan Blasér, Ronald Grant, Rosanna Weksberg, & Jacqueline Siegel‐Bartelt. (1998). MRI findings in macrocephaly‐cutis marmorata telangiectatica congenita. American Journal of Medical Genetics. 76(2). 165–167. 1 indexed citations
5.
Roessler, Erich, Karin Gaudenz, Elena Belloni, et al.. (1997). Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly. Human Genetics. 100(2). 172–181. 88 indexed citations
6.
Semina, Elena V., Rebecca S. Reiter, Nancy J. Leysens, et al.. (1996). Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nature Genetics. 14(4). 392–399. 720 indexed citations breakdown →
7.
McFarland, Janice G., et al.. (1993). Prenatal diagnosis of neonatal alloimmune thrombocytopenia using an allele‐specific oligonucleotide probe. Prenatal Diagnosis. 13(11). 1037–1042. 12 indexed citations
8.
Allen, Margot I. Van, Giorgio Filippi, Jacqueline Siegel‐Bartelt, et al.. (1993). Clinical variability within Brachmann‐de Lange syndrome: A proposed classification system. American Journal of Medical Genetics. 47(7). 947–958. 63 indexed citations
9.
Allen, Margot I. Van, Jacqueline Siegel‐Bartelt, Joanne Dixon, et al.. (1992). Constriction bands and limb reduction defects in two newborns with fetal ultrasound evidence for vascular disruption. American Journal of Medical Genetics. 44(5). 598–604. 30 indexed citations
10.
Narod, Steven A., Jacqueline Siegel‐Bartelt, Harold J. Hoffman, John M. Opitz, & James F. Reynolds. (1988). Cerebellar infarction in a patient with Waardenburg syndrome. American Journal of Medical Genetics. 31(4). 903–907. 5 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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