Milena Banjevic

3.1k citations

20 papers · 2.1k indexed · 1 hit paper · h-index 14

Pediatrics, Perinatology and Child Health top 0.5%
Genetics top 5%
Infectious Diseases top 5%
Molecular Biology
Social Psychology top 5%

Co-authors: Matthew Rabinowitz Allison Ryan Zachary Demko Matthew D. Hill Styrmir Sigurjonsson Bernhard Zimmermann E.B. Keverne Theodore Garland
Topics: Prenatal Screening and Diagnostics (17 papers)Genomic variations and chromosomal abnormalities (9 papers)Genetic Syndromes and Imprinting (6 papers)
Cited by: Pediatrics, Perinatology and Child Health Behavioral Neuroscience Developmental Biology
Journals: Science Nature Medicine Bioinformatics
Partner nations: United States United Kingdom Kenya

In The Last Decade

Milena Banjevic

20 papers receiving 2.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Are subordinates always stressed? a comparative analysis of rank differences in cortisol levels among primates

2003 506 citations David H. Abbott, E.B. Keverne et al. Hormones and Behavior profile →

Peers

Countries citing papers authored by Milena Banjevic

Since Specialization

Citations

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

Fields of papers citing papers by Milena Banjevic

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Milena Banjevic

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Whole-genome risk prediction of common diseases in human preimplantation embryos 2022 ·Nature Medicine ·Akash Kumar,(unknown),Milena Banjevic,Pauline C. Ng,(unknown),(unknown),(unknown),(unknown),(unknown),Brynn Levy,(unknown),(unknown),(unknown),Nam D. Tran,Peter Klatsky,Matthew Rabinowitz	32
2	Validation of an Enhanced Version of a Single-Nucleotide Polymorphism-Based Noninvasive Prenatal Test for Detection of Fetal Aneuploidies 2016 ·Fetal Diagnosis and Therapy ·Allison Ryan,Nathan Hunkapiller,Milena Banjevic,(unknown),Nicole L. Fong,(unknown),Zachary Demko,Bernhard Zimmermann,Styrmir Sigurjonsson,Susan J. Gross,Matthew D. Hill	41
3	Evidence of Selection against Complex Mitotic-Origin Aneuploidy during Preimplantation Development 2015 ·PLoS Genetics ·Rajiv C. McCoy,Zachary Demko,Allison Ryan,Milena Banjevic,Matthew D. Hill,Styrmir Sigurjonsson,Matthew Rabinowitz,Dmitri A. Petrov	153
4	Common Variants Spanning PLK4 Are Associated With Mitotic-Origin Aneuploidy in Human Embryos 2015 ·Obstetrical & Gynecological Survey ·Rajiv C. McCoy,Zachary Demko,Allison Ryan,Milena Banjevic,Matthew D. Hill,Styrmir Sigurjonsson,Matthew Rabinowitz,Hunter B. Fraser,Dmitri A. Petrov	8
5	Whole genome prediction for preimplantation genetic diagnosis 2015 ·Genome Medicine ·Akash Kumar,Allison Ryan,Jacob O. Kitzman,(unknown),Matthew W. Snyder,Styrmir Sigurjonsson,Choli Lee,Milena Banjevic,P.W. Zarutskie,Alexandra P. Lewis,Jay Shendure,Matthew Rabinowitz	25
6	Common variants spanning PLK4 are associated with mitotic-origin aneuploidy in human embryos 2015 ·Science ·Rajiv C. McCoy,Zachary Demko,Allison Ryan,Milena Banjevic,Matthew D. Hill,Styrmir Sigurjonsson,Matthew Rabinowitz,Hunter B. Fraser,Dmitri A. Petrov	83
7	Expanding the Scope of Noninvasive Prenatal Testing 2015 ·Obstetrical & Gynecological Survey ·Ronald J. Wapner,Joshua Babiarz,Brynn Levy,Melissa Stosic,Bernhard Zimmermann,Styrmir Sigurjonsson,Nicholas Wayham,Allison Ryan,Milena Banjevic,(unknown),Jing Hu,Megan P. Hall,Zachary Demko,Asim Siddiqui,Matthew Rabinowitz,Susan J. Gross,Matthew D. Hill,Peter Benn	2
8	Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes 2014 ·American Journal of Obstetrics and Gynecology ·Ronald J. Wapner,Joshua Babiarz,Brynn Levy,Melissa Stosic,Bernhard Zimmermann,Styrmir Sigurjonsson,Nicholas Wayham,Allison Ryan,Milena Banjevic,(unknown),Jing Hu,Megan P. Hall,Zachary Demko,Asim Siddiqui,Matthew Rabinowitz,Susan J. Gross,Matthew D. Hill,Peter Benn	224
9	Clinical experience and follow-up with large scale single-nucleotide polymorphism–based noninvasive prenatal aneuploidy testing 2014 ·American Journal of Obstetrics and Gynecology ·P. Dar,Kirsten J. Curnow,Susan J. Gross,Megan P. Hall,Melissa Stosic,Zachary Demko,Bernhard Zimmermann,Matthew D. Hill,Styrmir Sigurjonsson,Allison Ryan,Milena Banjevic,(unknown),(unknown),Charles M. Strom,Matthew Rabinowitz,Peter Benn	183
10	Single-Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in a High-Risk and Low-Risk Cohort 2014 ·Obstetrics and Gynecology ·Eugene Pergament,Howard Cuckle,Bernhard Zimmermann,Milena Banjevic,Styrmir Sigurjonsson,Allison Ryan,Megan P. Hall,Michael S. Dodd,(unknown),Melissa Stosic,Nikhil Chopra,Nathan Hunkapiller,Dennis E. Prosen,Sallie McAdoo,Zachary Demko,Asim Siddiqui,Matthew D. Hill,Matthew Rabinowitz	205
11	SNP‐based non‐invasive prenatal testing detects sex chromosome aneuploidies with high accuracy 2013 ·Prenatal Diagnosis ·Carole Samango‐Sprouse,Milena Banjevic,Allison Ryan,Styrmir Sigurjonsson,Bernhard Zimmermann,Matthew D. Hill,Megan P. Hall,(unknown),Jennifer Saucier,Zachary Demko,Matthew Rabinowitz	109
12	Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci 2012 ·Prenatal Diagnosis ·Bernhard Zimmermann,Matthew D. Hill,G. Gemelos,Zachary Demko,Milena Banjevic,Johan Banér,Allison Ryan,Styrmir Sigurjonsson,Nikhil Chopra,Michael S. Dodd,Brynn Levy,Matthew Rabinowitz	235
13	Origins and rates of aneuploidy in human blastomeres 2011 ·Fertility and Sterility ·Matthew Rabinowitz,Allison Ryan,G. Gemelos,Matthew D. Hill,Johan Banér,Cengiz Cinnioğlu,Milena Banjevic,D. Potter,Dmitri A. Petrov,Zachary Demko	105
14	Preclinical validation of a microarray method for full molecular karyotyping of blastomeres in a 24-h protocol 2010 ·Human Reproduction ·David S. Johnson,G. Gemelos,Johan Banér,Allison Ryan,Cengiz Cinnioğlu,Milena Banjevic,Robert M. Ross,Murat Alper,Brent Barrett,Jane Frederick,D. Potter,Barry Behr,Matthew Rabinowitz	178
15	Parental support for single gene PGD and simultaneous 24-chromosome screening reduces risks of allele misdiagnosis and transfer of aneuploid embryos 2009 ·Fertility and Sterility ·Matthew Rabinowitz,Barry Behr,David C. Potter,Robert M. Ross,Murat Alper,Milena Banjevic	2
16	Novel Technology for Simultaneous Reliable Measurement of Multiple Alleles And Copy Number Across 24 Chromosomes in Single Human Blastomeres 2008 ·Fertility and Sterility ·David S. Johnson,Matthew Rabinowitz,Cengiz Cinnioğlu,Jeffrey N. Keller,Milena Banjevic,J.D. Singer,Johan Banér,(unknown),Barry Behr	2
17	Reliable concurrent calling of multiple genetic alleles and 24-chromosome ploidy without embryo freezing using parental support™ technology (PS) 2008 ·Fertility and Sterility ·Matthew Rabinowitz,David S. Johnson,Julia Salzman,Milena Banjevic,Cengiz Cinnioğlu,Barry Behr	5
18	Accurate prediction of HIV-1 drug response from the reverse transcriptase and protease amino acid sequences using sparse models created by convex optimization 2005 ·Bioinformatics ·Matthew Rabinowitz,Lance Myers,Milena Banjevic,(unknown),(unknown),Jessica E. Haberer,(unknown),Roland Wolkowicz	20
19	Use of the l1 norm for selection of sparse parameter sets that accurately predict drug response phenotype from viral genetic sequences. 2005 ·PubMed ·(unknown),Milena Banjevic,(unknown),Lance Myers,Roland Wolkowicz,Jessica E. Haberer,Joshua B. Singer	2
20	Are subordinates always stressed? a comparative analysis of rank differences in cortisol levels among primatesbreakdown → 2003 ·Hormones and Behavior ·David H. Abbott,E.B. Keverne,Fred B. Bercovitch,Carol A. Shively,Sally P. Mendoza,Wendy Saltzman,Charles T. Snowdon,Toni E. Ziegler,Milena Banjevic,Theodore Garland,Robert M. Sapolsky	506

About Milena Banjevic

Milena Banjevic is a scholar working on Pediatrics, Perinatology and Child Health, Virology and Genetics, having authored 20 papers that have together received 2.1k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (17 papers), Genomic variations and chromosomal abnormalities (9 papers) and Genetic Syndromes and Imprinting (6 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (1.4k citations), Behavioral Neuroscience (128 citations) and Developmental Biology (59 citations). Milena Banjevic has collaborated with scholars based in United States, United Kingdom and Kenya. Frequent co-authors include Matthew Rabinowitz, Allison Ryan, Zachary Demko, Matthew D. Hill, Styrmir Sigurjonsson, Bernhard Zimmermann, E.B. Keverne, Theodore Garland, Wendy Saltzman and David H. Abbott. Their work appears in journals such as Science, Nature Medicine and Bioinformatics.

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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