Bianca Russell

426 total citations
18 papers, 142 citations indexed

About

Bianca Russell is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Bianca Russell has authored 18 papers receiving a total of 142 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 10 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Bianca Russell's work include Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Bianca Russell is often cited by papers focused on Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Bianca Russell collaborates with scholars based in United States, Canada and United Kingdom. Bianca Russell's co-authors include John M. Graham, Wen‐Hann Tan, Rachel Harrison, Benjamin M. Helm, Nancy Kramer, Avi Z. Rosenberg, Samantha A. Schrier Vergano, Leslie G. Biesecker, Jennifer J. Johnston and William J. Rhead and has published in prestigious journals such as PEDIATRICS, Cancer Research and Epilepsia.

In The Last Decade

Bianca Russell

14 papers receiving 140 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bianca Russell United States	7	77	71	20	18	13	18	142
Juliane Eckhold Germany	8	116 1.5×	66 0.9×	22 1.1×	12 0.7×	19 1.5×	10	202
Colleen M. Carlston United States	8	122 1.6×	112 1.6×	9 0.5×	28 1.6×	13 1.0×	13	234
Natalya Karp Canada	8	53 0.7×	46 0.6×	15 0.8×	7 0.4×	21 1.6×	14	134
Stefano Petrocchi Italy	8	84 1.1×	129 1.8×	16 0.8×	8 0.4×	15 1.2×	15	236
Dmitrijs Rots Latvia	8	75 1.0×	26 0.4×	27 1.4×	11 0.6×	6 0.5×	30	181
Dennis W. Bartholomew United States	8	121 1.6×	48 0.7×	14 0.7×	8 0.4×	12 0.9×	17	192
Katalin Szakszon Hungary	10	178 2.3×	103 1.5×	16 0.8×	7 0.4×	26 2.0×	29	276
Yanling Teng China	9	130 1.7×	69 1.0×	31 1.6×	9 0.5×	6 0.5×	33	195
Connie T. R. M. Stumpel Netherlands	7	92 1.2×	110 1.5×	7 0.3×	20 1.1×	11 0.8×	9	197
Katherine R. Chao United States	8	120 1.6×	45 0.6×	7 0.3×	17 0.9×	8 0.6×	16	177

Countries citing papers authored by Bianca Russell

Since Specialization

Citations

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

Fields of papers citing papers by Bianca Russell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bianca Russell

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

All Works

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18 of 18 papers shown

Rodan, Lance H., Joan M. Stoler, Emily Chen, et al.. (2025). Genetic Evaluation of the Child With Intellectual Disability or Global Developmental Delay: Clinical Report. PEDIATRICS. 156(1). 1 indexed citations

Scheuerle, Angela E., Timothy A. Geleske, Paula Goldenberg, et al.. (2025). Health Supervision for Children With 22q11.2 Deletion Syndrome: Clinical Report. PEDIATRICS. 156(2).

Awamleh, Zain, et al.. (2024). ASXL1 truncating variants in BOS and myeloid leukemia drive shared disruption of Wnt-signaling pathways but have differential isoform usage of RUNX3. BMC Medical Genomics. 17(1). 282–282. 2 indexed citations

Russell, Bianca, et al.. (2024). Complex genomic rearrangements of the Y chromosome in a premature infant. Molecular Cytogenetics. 17(1). 19–19.

Ngo, Jacqueline, Aran Groves, Dennis J. Chia, et al.. (2024). Multi‐disciplinary team approach for pediatric hemimegalencephaly: Insights from a single institutional case series. Epilepsia Open. 9(6). 2510–2517.

Russell, Bianca, et al.. (2024). Abstract 6375: Genetic testing station increases access to germline genetic testing. Cancer Research. 84(6_Supplement). 6375–6375. 1 indexed citations

Russell, Bianca, et al.. (2023). Examining the neurodevelopmental and motor phenotypes of Bohring-Opitz syndrome (ASXL1) and Bainbridge-Ropers syndrome (ASXL3). Frontiers in Neuroscience. 17. 1244176–1244176. 3 indexed citations

Awamleh, Zain, et al.. (2023). Multiomics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and noncanonical Wnt signaling dysregulation. JCI Insight. 8(10). 7 indexed citations

Goël, Keshav, H. Westley Phillips, Jia‐Shu Chen, et al.. (2023). Hemispheric epilepsy surgery for hemimegalencephaly: The UCLA experience. Epilepsia. 65(1). 57–72. 6 indexed citations

10.

Russell, Bianca, et al.. (2023). Clinical findings in 39 individuals with Bohring–Opitz syndrome from a global patient‐driven registry with implications for tumor surveillance and recurrence risk. American Journal of Medical Genetics Part A. 191(4). 1050–1058. 6 indexed citations

11.

Awamleh, Zain, Eric Chater‐Diehl, Sanaa Choufani, et al.. (2022). DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes. European Journal of Human Genetics. 30(6). 695–702. 14 indexed citations

12.

Chenbhanich, Jirat, Yan Hu, Steven W. Hetts, et al.. (2021). Segmental overgrowth and aneurysms due to mosaic PDGFRB p.(Tyr562Cys). American Journal of Medical Genetics Part A. 185(5). 1430–1436. 9 indexed citations

13.

Efthymiou, Stéphanie, Marina Dutra‐Clarke, Reza Maroofian, et al.. (2021). Expanding the phenotype of PIGS‐associated early onset epileptic developmental encephalopathy. Epilepsia. 62(2). e35–e41. 11 indexed citations

14.

ZIEGLER, M. L., Bianca Russell, Angelica D’Amore, et al.. (2020). Blended Phenotype of Silver-Russell Syndrome and SPG50 Caused by Maternal Isodisomy of Chromosome 7. Neurology Genetics. 7(1). e544–e544. 6 indexed citations

15.

Russell, Bianca, Diana Rigueur, K. Nicole Weaver, et al.. (2019). Homozygous missense variant in BMPR1A resulting in BMPR signaling disruption and syndromic features. Molecular Genetics & Genomic Medicine. 7(11). e969–e969. 7 indexed citations

16.

Russell, Bianca, Wen‐Hann Tan, & John M. Graham. (2018). Bohring-Opitz Syndrome. Europe PMC (PubMed Central). 6 indexed citations

17.

Russell, Bianca, Jennifer J. Johnston, Leslie G. Biesecker, et al.. (2015). Clinical management of patients with ASXL1 mutations and Bohring–Opitz syndrome, emphasizing the need for Wilms tumor surveillance. American Journal of Medical Genetics Part A. 167(9). 2122–2131. 47 indexed citations

18.

Russell, Bianca & John M. Graham. (2013). Expanding our knowledge of conditions associated with the ASXL gene family. Genome Medicine. 5(2). 16–16. 16 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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