Milena Babic

1.9k total citations
15 papers, 138 citations indexed

About

Milena Babic is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Milena Babic has authored 15 papers receiving a total of 138 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Hematology and 4 papers in Genetics. Recurrent topics in Milena Babic's work include Acute Myeloid Leukemia Research (5 papers), RNA modifications and cancer (3 papers) and RNA Research and Splicing (3 papers). Milena Babic is often cited by papers focused on Acute Myeloid Leukemia Research (5 papers), RNA modifications and cancer (3 papers) and RNA Research and Splicing (3 papers). Milena Babic collaborates with scholars based in Australia, Malaysia and Belarus. Milena Babic's co-authors include Hamish S. Scott, Christopher N Hahn, Parvathy Venugopal, Jinghua Feng, Andreas Schreiber, Peter J Brautigan, Steven Lane, Richard J. D’Andrea, Manuela Klingler‐Hoffmann and Paul Wang and has published in prestigious journals such as Blood, Scientific Reports and Leukemia.

In The Last Decade

Milena Babic

14 papers receiving 137 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Milena Babic Australia	6	92	40	30	24	19	15	138
Boris Skrobek United Kingdom	2	63 0.7×	51 1.3×	48 1.6×	23 1.0×	37 1.9×	2	140
Julia Kolarova Germany	9	127 1.4×	13 0.3×	76 2.5×	28 1.2×	14 0.7×	20	190
Courtney E. Hershberger United States	7	176 1.9×	63 1.6×	16 0.5×	36 1.5×	21 1.1×	20	237
Yael Dinur Schejter Israel	7	38 0.4×	42 1.1×	34 1.1×	20 0.8×	16 0.8×	14	169
Te Ling China	8	272 3.0×	43 1.1×	48 1.6×	23 1.0×	36 1.9×	12	322
Astrid Novosel Germany	4	99 1.1×	27 0.7×	7 0.2×	83 3.5×	16 0.8×	5	162
Christina Sternberg Austria	6	145 1.6×	25 0.6×	19 0.6×	10 0.4×	18 0.9×	6	188
Jennifer A. Bassetti United States	2	123 1.3×	9 0.2×	38 1.3×	28 1.2×	7 0.4×	4	173
Joanna Madzio Poland	6	36 0.4×	23 0.6×	31 1.0×	26 1.1×	7 0.4×	16	110
Insha Mushtaq United States	9	90 1.0×	10 0.3×	22 0.7×	20 0.8×	7 0.4×	12	147

Countries citing papers authored by Milena Babic

Since Specialization

Citations

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

Fields of papers citing papers by Milena Babic

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Milena Babic

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

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

Vannucci, Luca, Dmitry Stakheev, P. Tenti, et al.. (2025). The tumor immune microenvironment as a target for nano-therapies and patient-tailored treatments.. 8(CITIM). 52–52.

Ghaoui, Roula, Thuong Ha, Jennifer Kerkhof, et al.. (2023). Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis. Neuromuscular Disorders. 33(6). 484–489. 3 indexed citations

Byrne, Alicia B., Jinghua Feng, Thuong Ha, et al.. (2021). Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia. BMC Medical Genomics. 14(1). 64–64. 5 indexed citations

Arts, Peer, Alicia B. Byrne, Tristan Hardy, et al.. (2020). Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1‐related syndrome. American Journal of Medical Genetics Part A. 182(5). 1273–1277. 11 indexed citations

Venugopal, Parvathy, Lucia Gagliardi, Cecily Forsyth, et al.. (2020). Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss. BMC Medical Genetics. 21(1). 35–35. 2 indexed citations

Byrne, Alicia B., Shuji Mizumoto, Peer Arts, et al.. (2020). Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesis. Journal of Medical Genetics. 57(7). 454–460. 9 indexed citations

Hahn, Christopher N, Milena Babic, Peter J Brautigan, et al.. (2019). Australian Familial Haematological Cancer Study - Findings from 15 Years of Aggregated Clinical, Genomic and Transcriptomic Data. Blood. 134(Supplement_1). 1439–1439. 1 indexed citations

Sousa, Sunita M C De, Paul Wang, Stephen Santoreneos, et al.. (2019). The Genomic Landscape of Sporadic Prolactinomas. Endocrine Pathology. 30(4). 318–328. 18 indexed citations

Brown, Anna, Milena Babic, Andreas Schreiber, et al.. (2019). Familial Clustering of Hematological Malignancies: Harbingers of Wider Germline Cancer Susceptibility. Blood. 134(Supplement_1). 3794–3794. 1 indexed citations

10.

Hahn, Christopher N, Milena Babic, Jinghua Feng, et al.. (2017). Duplication on Chromosome 14q Identified in Familial Predisposition to Myeloid Malignancies and Myeloproliferative Neoplasms. Blood. 130. 492–492. 3 indexed citations

11.

Chong, Chan‐Eng, Parvathy Venugopal, Philippa H. Stokes, et al.. (2017). Differential effects on gene transcription and hematopoietic differentiation correlate with GATA2 mutant disease phenotypes. Leukemia. 32(1). 194–202. 44 indexed citations

12.

Ling, King‐Hwa, Peter J Brautigan, Sarah Moore, et al.. (2016). Derivation of an endogenous small RNA from double-stranded Sox4 sense and natural antisense transcripts in the mouse brain. Genomics. 107(2-3). 88–99. 13 indexed citations

13.

Ling, King‐Hwa, Peter J Brautigan, Sarah Moore, et al.. (2016). In depth analysis of the Sox4 gene locus that consists of sense and natural antisense transcripts. Data in Brief. 7. 282–290. 3 indexed citations

14.

Hu, Zhiqiang, Hamish S. Scott, Guangrong Qin, et al.. (2015). Revealing Missing Human Protein Isoforms Based on Ab Initio Prediction, RNA-seq and Proteomics. Scientific Reports. 5(1). 10940–10940. 22 indexed citations

15.

Hiwase, Devendra, Christopher N Hahn, Milena Babic, et al.. (2014). Clonal Diversity of Recurrently Mutated Genes in Myelodysplastic Syndromes. Blood. 124(21). 4634–4634. 3 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