Jacquelyn Roberson

539 total citations
18 papers, 341 citations indexed

About

Jacquelyn Roberson is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jacquelyn Roberson has authored 18 papers receiving a total of 341 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jacquelyn Roberson's work include Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Prenatal Screening and Diagnostics (4 papers). Jacquelyn Roberson is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Prenatal Screening and Diagnostics (4 papers). Jacquelyn Roberson collaborates with scholars based in United States, Canada and Australia. Jacquelyn Roberson's co-authors include Lester Weiss, Daniel L. Van Dyke, Anne E. Wiktor, V. Ramesh Babu, Isabelle Schuffenecker, Nancie Petrucelli, Charles E. Jackson, Andrew Saxe, Gerald L. Feldman and Gilbert Lenoir and has published in prestigious journals such as PLoS ONE, The Journal of Pediatrics and Journal of Medical Genetics.

In The Last Decade

Jacquelyn Roberson

17 papers receiving 333 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jacquelyn Roberson United States 10 223 151 81 75 50 18 341
Jack H. Jung Canada 13 208 0.9× 218 1.4× 61 0.8× 27 0.4× 83 1.7× 19 411
Jaime Garcia‐Heras United States 14 244 1.1× 208 1.4× 79 1.0× 21 0.3× 93 1.9× 25 440
Natalie Canham United Kingdom 10 198 0.9× 158 1.0× 20 0.2× 76 1.0× 39 0.8× 20 388
Antoinet C.J. Gijsbers Netherlands 12 356 1.6× 212 1.4× 67 0.8× 31 0.4× 94 1.9× 15 426
Maria Paola Recalcati Italy 11 240 1.1× 191 1.3× 46 0.6× 9 0.1× 89 1.8× 21 378
Chiara Castronovo Italy 9 183 0.8× 122 0.8× 49 0.6× 10 0.1× 51 1.0× 16 275
C. Schaap Netherlands 6 88 0.4× 61 0.4× 12 0.1× 67 0.9× 17 0.3× 8 189
J.G. Dauwerse Netherlands 6 129 0.6× 211 1.4× 52 0.6× 14 0.2× 17 0.3× 7 307
Gita Tan-Sindhunata Netherlands 8 172 0.8× 189 1.3× 21 0.3× 18 0.2× 42 0.8× 12 439
Konstantina Kosma Greece 10 137 0.6× 130 0.9× 17 0.2× 12 0.2× 37 0.7× 30 288

Countries citing papers authored by Jacquelyn Roberson

Since Specialization
Citations

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

Fields of papers citing papers by Jacquelyn Roberson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacquelyn Roberson

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

All Works

18 of 18 papers shown
1.
2.
Roberson, Jacquelyn, et al.. (2022). Recurrence Rate for Isolated Elevated Maternal Serum Alpha-Fetoprotein Levels and Pregnancy Outcomes. Genetic Testing and Molecular Biomarkers. 26(9). 443–448. 1 indexed citations
3.
Stockton, David W., et al.. (2021). Biallelic Variants in LAMB1 Causing Hydranencephaly: A Severe Phenotype of a Rare Malformative Encephalopathy. American Journal of Perinatology Reports. 11(1). e26–e28. 4 indexed citations
4.
Saunders, Darren N., Elizabeth A. Tindall, Robert F. Shearer, et al.. (2012). A Novel SERPINA1 Mutation Causing Serum Alpha1-Antitrypsin Deficiency. PLoS ONE. 7(12). e51762–e51762. 10 indexed citations
5.
Everman, David B., Robert Lyle, Michael J. Bamshad, et al.. (2006). Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non‐syndromic split‐hand/foot malformation. American Journal of Medical Genetics Part A. 140A(13). 1375–1383. 17 indexed citations
6.
Roberson, Jacquelyn, et al.. (2001). Prenatal diagnosis of 22q11.2 deletion when ultrasound examination reveals a heart defect. Genetics in Medicine. 3(1). 65–66. 17 indexed citations
7.
Feldman, Gerald L., Peter Ainsworth, Isabelle Schuffenecker, et al.. (2000). Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG→ATG) mutation. Surgery. 128(1). 93–98. 84 indexed citations
8.
Feldman, Gerald L., Isabelle Schuffenecker, Gilbert Lenoir, et al.. (1999). Variable expressivity of Familial Medullary Thyroid Carcinoma (FMTC) due to a RET V804M (GTGG→ATG) mutation in two families: Reluctance of gene carriers to accept prophylactic thyroidectomy. Genetics in Medicine. 1(2). 45–45. 1 indexed citations
9.
Pratt, Victoria M., Jacquelyn Roberson, Lester Weiss, & Daniel L. Van Dyke. (1998). Duplication 6q21q23 in two unrelated patients. American Journal of Medical Genetics. 80(2). 112–114. 10 indexed citations
10.
Roberson, Jacquelyn, et al.. (1993). Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies. American Journal of Medical Genetics. 46(4). 438–440. 5 indexed citations
11.
Dyke, Daniel L. Van, Anne E. Wiktor, Dorothy A. Miller, et al.. (1992). Ullrich‐Turner syndrome with a small ring X chromosome and presence of mental retardation. American Journal of Medical Genetics. 43(6). 996–1005. 72 indexed citations
12.
Roberson, Jacquelyn, et al.. (1991). Mother and son with deletion of 3p25‐pter. American Journal of Medical Genetics. 39(2). 130–132. 18 indexed citations
13.
Dyke, Daniel L. Van, Anne E. Wiktor, Jacquelyn Roberson, & Lester Weiss. (1991). Mental retardation in Turner syndrome. The Journal of Pediatrics. 118(3). 415–417. 38 indexed citations
14.
Bodrug, Sharon, Jacquelyn Roberson, Lester Weiss, et al.. (1990). Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.. Journal of Medical Genetics. 27(7). 426–432. 33 indexed citations
15.
Roberson, Jacquelyn, et al.. (1990). Breast cancer metastatic to the foot with massive bone loss.. PubMed. 19(10). 877–9. 2 indexed citations
16.
Dyke, Daniel L. Van, Wendy L. Flejter, M J Worsham, et al.. (1986). A practical metaphase marker of the inactive X chromosome.. PubMed. 39(1). 88–95. 20 indexed citations
17.
Dyke, Daniel L. Van, et al.. (1985). 868 A PRACTICAL METAPHASE MARKER OF THE INACTIVE X CHROMOSOME. Pediatric Research. 19(4). 255A–255A. 7 indexed citations
18.
Roberson, Jacquelyn, et al.. (1984). PRENATAL DIAGNOSIS OF A GIRL WITH MUSCULAR DYSTROPHY CAUSED BY DE NOVO t(X;4) (p21;q35). Pediatric Research. 18. 225A–225A. 2 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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