Helen J. Lawce

963 total citations
31 papers, 575 citations indexed

About

Helen J. Lawce is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Helen J. Lawce has authored 31 papers receiving a total of 575 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 10 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Helen J. Lawce's work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Helen J. Lawce is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Helen J. Lawce collaborates with scholars based in United States, Netherlands and Canada. Helen J. Lawce's co-authors include Susan B. Olson, R. Ellen Magenis, Kimberly J. Bussey, Ken Gatter, Atiya Mansoor, Megan L. Troxell, Roger Giller, Mark Krailo, Dagmar K. Kalousek and Stephen A. Heifetz and has published in prestigious journals such as American Journal of Obstetrics and Gynecology, Fertility and Sterility and Leukemia.

In The Last Decade

Helen J. Lawce

31 papers receiving 546 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Helen J. Lawce United States 14 175 169 146 141 134 31 575
Max M. van Noesel Netherlands 16 445 2.5× 291 1.7× 133 0.9× 232 1.6× 68 0.5× 44 1.0k
Les Coulton United Kingdom 15 292 1.7× 263 1.6× 111 0.8× 51 0.4× 60 0.4× 22 761
R. Haas Germany 13 173 1.0× 155 0.9× 194 1.3× 95 0.7× 49 0.4× 48 820
Herman Van den Berghe Belgium 10 302 1.7× 71 0.4× 80 0.5× 162 1.1× 89 0.7× 12 708
Susan Rowe United States 14 404 2.3× 143 0.8× 78 0.5× 224 1.6× 87 0.6× 18 833
Denisa Ilenčíková Slovakia 15 301 1.7× 227 1.3× 109 0.7× 96 0.7× 190 1.4× 40 851
A. Al Saadi United States 12 201 1.1× 143 0.8× 132 0.9× 46 0.3× 160 1.2× 16 726
Beata Grygalewicz Poland 14 243 1.4× 159 0.9× 236 1.6× 125 0.9× 119 0.9× 40 659
J.P. Vannier France 10 203 1.2× 185 1.1× 49 0.3× 78 0.6× 29 0.2× 26 659
Marie Jarošová Czechia 17 264 1.5× 136 0.8× 35 0.2× 95 0.7× 58 0.4× 87 766

Countries citing papers authored by Helen J. Lawce

Since Specialization
Citations

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

Fields of papers citing papers by Helen J. Lawce

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Helen J. Lawce

This figure shows the co-authorship network connecting the top 25 collaborators of Helen J. Lawce. A scholar is included among the top collaborators of Helen J. Lawce 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 Helen J. Lawce. Helen J. Lawce 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.
Long, Thomas, Helen J. Lawce, Stephen Moore, et al.. (2015). The New Equivocal. American Journal of Clinical Pathology. 144(2). 253–262. 45 indexed citations
2.
Lawce, Helen J. & Susan B. Olson. (2009). FISH testing for deletions of chromosome 6q21 and 6q23 in hematologic neoplastic disorders.. PubMed. 35(4). 167–9. 1 indexed citations
3.
Lawce, Helen J., et al.. (2008). Cytogenetic analysis of a hemosiderotic fibrolipomatous tumor. Cancer Genetics and Cytogenetics. 182(2). 140–143. 31 indexed citations
4.
Troxell, Megan L., Charles D. Bangs, Helen J. Lawce, et al.. (2006). Evaluation of Her-2/neu Status in Carcinomas With Amplified Chromosome 17 Centromere Locus. American Journal of Clinical Pathology. 126(5). 709–716. 50 indexed citations
5.
Troxell, Megan L., Charles D. Bangs, Helen J. Lawce, et al.. (2006). Evaluation of Her-2/neu Status in Carcinomas With Amplified Chromosome 17 Centromere Locus. American Journal of Clinical Pathology. 126(5). 709–716. 4 indexed citations
6.
Brown, Michael G., Helen J. Lawce, Joseph Gilhooly, et al.. (2005). Meiotic exchange event within the stalk region of an inverted chromosome 22 results in a recombinant chromosome with duplication of the distal long arm. American Journal of Medical Genetics Part A. 138A(4). 355–360. 21 indexed citations
7.
Akkari, Yassmine, et al.. (2005). Y chromosome heterochromatin of differing lengths in two cell populations of the same individual. Prenatal Diagnosis. 25(4). 304–306. 5 indexed citations
8.
Gatter, Ken, Susan B. Olson, Helen J. Lawce, & Anne E. Rader. (2005). Trisomy 8 as the sole cytogenetic abnormality in a case of extraskeletal mesenchymal chondrosarcoma. Cancer Genetics and Cytogenetics. 159(2). 151–154. 15 indexed citations
9.
Mansoor, Atiya, et al.. (2004). Myxoinflammatory fibroblastic sarcoma with complex supernumerary ring chromosomes composed of chromosome 3 segments. Cancer Genetics and Cytogenetics. 152(1). 61–65. 38 indexed citations
10.
Sampson, Jone E., Nadia Ouhibi, Helen J. Lawce, et al.. (2004). The role for preimplantation genetic diagnosis in balanced translocation carriers. American Journal of Obstetrics and Gynecology. 190(6). 1707–1711. 14 indexed citations
11.
12.
Ouhibi, Nadia, Phillip E. Patton, Susan B. Olson, et al.. (2003). Preimplantation genetic diagnosis: does embryo biopsy for PGD compromise clinical outcome?. Fertility and Sterility. 79. 23–23. 1 indexed citations
13.
Bussey, Kimberly J., Helen J. Lawce, Xiao Ou Shu, et al.. (2001). Chromosomes 1 and 12 abnormalities in pediatric germ cell tumors by interphase fluorescence in situ hybridization. Cancer Genetics and Cytogenetics. 125(2). 112–118. 19 indexed citations
14.
Bussey, Kimberly J., Helen J. Lawce, Xiao Ou Shu, et al.. (2001). SNRPN methylation patterns in germ cell tumors as a reflection of primordial germ cell development. Genes Chromosomes and Cancer. 32(4). 342–352. 36 indexed citations
15.
Bussey, Kimberly J., Helen J. Lawce, Susan B. Olson, et al.. (1999). Chromosome abnormalities of eighty-one pediatric germ cell tumors: Sex-, age-, site-, and histopathology-related differences?a Children's Cancer Group study. Genes Chromosomes and Cancer. 25(2). 134–146. 92 indexed citations
16.
Lawce, Helen J., et al.. (1996). Complex translocation (7;22) identified in an epithelioid hemangioendothelioma. Cancer Genetics and Cytogenetics. 92(2). 116–121. 33 indexed citations
17.
Magenis, R. Ellen, et al.. (1995). Prenatal diagnosis of chromosome 15 abnormalities in the Prader‐Willi/Angelman syndrome region by traditional and molecular cytogenetics. American Journal of Medical Genetics. 55(4). 444–452. 4 indexed citations
18.
Knutsen, Turid, et al.. (1991). Chromosome analysis guidelines preliminary report. Cancer Genetics and Cytogenetics. 52(1). 11–17. 13 indexed citations
19.
Knutsen, Tor, et al.. (1990). Chromosome analysis guidelines – preliminary report. Cytogenetic and Genome Research. 54(1-2). 1–4. 11 indexed citations
20.
Knight, Louise A., et al.. (1984). Prenatal diagnosis of 45,X/46,XX mosaicism: True mosaicism in only one of four primary cultures. Prenatal Diagnosis. 4(2). 143–146. 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026