Liane Abrams

784 total citations
16 papers, 526 citations indexed

About

Liane Abrams is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Liane Abrams has authored 16 papers receiving a total of 526 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Cognitive Neuroscience. Recurrent topics in Liane Abrams's work include Genetics and Neurodevelopmental Disorders (8 papers), Autism Spectrum Disorder Research (5 papers) and Genomic variations and chromosomal abnormalities (3 papers). Liane Abrams is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Autism Spectrum Disorder Research (5 papers) and Genomic variations and chromosomal abnormalities (3 papers). Liane Abrams collaborates with scholars based in United States, Thailand and Australia. Liane Abrams's co-authors include Brenda Finucane, Allyn McConkie‐Rosell, Amy Cronister, Robin L. Bennett, Sarah M. Coffey, Elizabeth Berry‐Kravis, Randi J. Hagerman, Louise W. Gane, Flora Tassone and B. Pettersen and has published in prestigious journals such as PEDIATRICS, Movement Disorders and American Journal of Medical Genetics.

In The Last Decade

Liane Abrams

16 papers receiving 510 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Liane Abrams United States	8	422	238	216	97	55	16	526
Markéta Havlovičová Czechia	14	274 0.6×	244 1.0×	215 1.0×	135 1.4×	27 0.5×	33	643
Martine Borghgraef Belgium	18	780 1.8×	381 1.6×	408 1.9×	50 0.5×	76 1.4×	54	925
Ravinesh A. Kumar United States	10	508 1.2×	364 1.5×	278 1.3×	83 0.9×	73 1.3×	16	767
Alexis Rea United States	6	321 0.8×	218 0.9×	279 1.3×	73 0.8×	14 0.3×	7	619
Teresa S. Miguel Portugal	9	358 0.8×	159 0.7×	404 1.9×	81 0.8×	38 0.7×	11	597
J.J.A. Holden Canada	14	281 0.7×	219 0.9×	250 1.2×	57 0.6×	27 0.5×	21	631
Athina Ververi Greece	11	153 0.4×	136 0.6×	188 0.9×	53 0.5×	48 0.9×	33	447
Christopher M. McGraw United States	11	468 1.1×	336 1.4×	324 1.5×	73 0.8×	34 0.6×	19	637
Daniel Moreno‐De‐Luca United States	9	413 1.0×	179 0.8×	389 1.8×	26 0.3×	51 0.9×	16	677
Assunção Ataíde Portugal	8	433 1.0×	196 0.8×	501 2.3×	55 0.6×	19 0.3×	8	691

Countries citing papers authored by Liane Abrams

Since Specialization

Citations

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

Fields of papers citing papers by Liane Abrams

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Liane Abrams

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

All Works

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16 of 16 papers shown

1.

Abrams, Liane, et al.. (2024). Experiences of individuals receiving “Not Parent Expected” results through direct‐to‐consumer genetic testing. Journal of Genetic Counseling. 34(3). e1977–e1977. 1 indexed citations

2.

Becker, Julia, et al.. (2021). Experiences of individuals receiving “Not Parent Expected” (NPE) results through direct-to-consumer genetic testing. Molecular Genetics and Metabolism. 132. S289–S289. 1 indexed citations

3.

Abrams, Liane, et al.. (2015). Contraction of a Maternal Fragile X Mental Retardation 1 Premutation Allele. Journal of Medical Cases. 6(12). 547–553. 2 indexed citations

4.

Abrams, Liane, et al.. (2015). Contraction of a Maternal Fragile X Mental Retardation 1 Premutation Allele. Journal of Medical Cases. 6(12). 547–553. 1 indexed citations

5.

Zanko, Andrea & Liane Abrams. (2014). Case Report: Concurrent Wilson Disease and Huntington Disease: Lightning Can Strike Twice. Journal of Genetic Counseling. 24(1). 40–45. 1 indexed citations

6.

Finucane, Brenda, Liane Abrams, Amy Cronister, et al.. (2012). Genetic Counseling and Testing for FMR1 Gene Mutations: Practice Guidelines of the National Society of Genetic Counselors. Journal of Genetic Counseling. 21(6). 752–760. 56 indexed citations

7.

Abrams, Liane, Amy Cronister, W. Ted Brown, et al.. (2012). Newborn, Carrier, and Early Childhood Screening Recommendations for Fragile X. PEDIATRICS. 130(6). 1126–1135. 29 indexed citations

8.

Berry‐Kravis, Elizabeth, Liane Abrams, Sarah M. Coffey, et al.. (2007). Fragile X‐associated tremor/ataxia syndrome: Clinical features, genetics, and testing guidelines. Movement Disorders. 22(14). 2018–2030. 233 indexed citations

9.

McConkie‐Rosell, Allyn, Liane Abrams, Brenda Finucane, et al.. (2007). Recommendations from Multi‐disciplinary Focus Groups on Cascade Testing and Genetic Counseling for Fragile X‐associated Disorders. Journal of Genetic Counseling. 16(5). 593–606. 48 indexed citations

10.

McConkie‐Rosell, Allyn, Brenda Finucane, Amy Cronister, et al.. (2005). Genetic Counseling for Fragile X Syndrome: Updated Recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling. 14(4). 249–270. 85 indexed citations

11.

McConkie‐Rosell, Allyn, Brenda Finucane, Amy Cronister, et al.. (2005). Genetic Counseling for Fragile X Syndrome: Updated Recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling. 14(4). 249–270. 4 indexed citations

12.

Lammer, Edward J. & Liane Abrams. (2002). Genitopatellar syndrome: Delineating the anomalies of female genitalia. American Journal of Medical Genetics. 111(3). 316–318. 11 indexed citations

13.

Abrams, Liane & Seymour Kessler. (2002). The Inner World of the Genetic Counselor. Journal of Genetic Counseling. 11(1). 5–17. 16 indexed citations

14.

Lammer, Edward J., et al.. (2001). Autosomal recessive tetralogy of Fallot, unusual facies, communicating hydrocephalus, and delayed language development: a new syndrome?. Clinical Dysmorphology. 10(1). 9–13. 5 indexed citations

15.

Abrams, Liane, et al.. (2000). Tetrasomy 15q25→qter: Cytogenetic and molecular characterization of an analphoid supernumerary marker chromosome. American Journal of Medical Genetics. 93(5). 393–398. 3 indexed citations

16.

Abrams, Liane, et al.. (2000). Tetrasomy 15q25?qter: Cytogenetic and molecular characterization of an analphoid supernumerary marker chromosome. American Journal of Medical Genetics. 93(5). 393–398. 30 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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