B. Pettersen

931 total citations
12 papers, 406 citations indexed

About

B. Pettersen is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Clinical Psychology. According to data from OpenAlex, B. Pettersen has authored 12 papers receiving a total of 406 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 7 papers in Genetics and 3 papers in Clinical Psychology. Recurrent topics in B. Pettersen's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (4 papers) and Family and Disability Support Research (3 papers). B. Pettersen is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (4 papers) and Family and Disability Support Research (3 papers). B. Pettersen collaborates with scholars based in United States and Paraguay. B. Pettersen's co-authors include Ruth B. Lathi, Styrmir Sigurjonsson, Matthew Rabinowitz, Zachary Demko, Melissa Maisenbacher, Robin L. Bennett, Megan P. Hall, Vimla S. Aggarwal, Brynn Levy and Allyn McConkie‐Rosell and has published in prestigious journals such as Fertility and Sterility, Obstetrics and Gynecology and Journal of Medical Genetics.

In The Last Decade

B. Pettersen

12 papers receiving 369 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
B. Pettersen United States 8 254 207 112 77 51 12 406
Mitsuyo Tanemura Japan 12 148 0.6× 85 0.4× 34 0.3× 43 0.6× 56 1.1× 27 359
Sigal Klipstein United States 10 261 1.0× 147 0.7× 154 1.4× 111 1.4× 7 0.1× 29 501
Bent Nørgaard‐Pedersen Denmark 9 153 0.6× 66 0.3× 39 0.3× 86 1.1× 21 0.4× 10 300
Martin Schorsch Germany 17 320 1.3× 235 1.1× 246 2.2× 405 5.3× 17 0.3× 26 786
Jovana P. Lekovich United States 18 379 1.5× 76 0.4× 543 4.8× 70 0.9× 28 0.5× 49 914
Violaine Kerbrat France 12 313 1.2× 115 0.6× 107 1.0× 250 3.2× 14 0.3× 27 547
Christina N. Cordeiro United States 11 82 0.3× 22 0.1× 114 1.0× 46 0.6× 15 0.3× 16 354
Susan Gitlin United States 11 482 1.9× 168 0.8× 334 3.0× 146 1.9× 4 0.1× 12 715
Suonavy Khung‐Savatovsky France 8 112 0.4× 65 0.3× 39 0.3× 67 0.9× 9 0.2× 15 335
Elena Lopez‐Rangel Canada 11 50 0.2× 142 0.7× 25 0.2× 97 1.3× 33 0.6× 19 297

Countries citing papers authored by B. Pettersen

Since Specialization
Citations

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

Fields of papers citing papers by B. Pettersen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B. Pettersen

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

All Works

12 of 12 papers shown
1.
Maisenbacher, Melissa, B. Pettersen, Michael Young, et al.. (2017). Incidence of the 22q11.2 deletion in a large cohort of miscarriage samples. Molecular Cytogenetics. 10(1). 6–6. 24 indexed citations
2.
Pettersen, B., et al.. (2015). Pregnancy outcomes following 24-chromosome preimplantation genetic diagnosis in couples with balanced reciprocal or Robertsonian translocations. Fertility and Sterility. 103(4). 1037–1042. 49 indexed citations
3.
Levy, Brynn, Styrmir Sigurjonsson, B. Pettersen, et al.. (2014). Genomic Imbalance in Products of Conception. Obstetrics and Gynecology. 124(2). 202–209. 158 indexed citations
4.
Rabinowitz, Matthew, Melissa Savage, B. Pettersen, et al.. (2014). Noninvasive Cell-Free DNA-Based Prenatal Detection of Microdeletions Using Single Nucleotide Polymorphism–Targeted Sequencing. Obstetrics and Gynecology. 123(Supplement 1). 167S–167S. 13 indexed citations
5.
Rabinowitz, Matthew, et al.. (2014). Noninvasive Aneuploidy Detection by Multiplexed Amplification and Sequencing of Polymorphic Loci. Obstetrics and Gynecology. 123(Supplement 1). 167S–167S. 7 indexed citations
6.
Rabinowitz, Matthew, B. Pettersen, Anh Le, G. Gemelos, & David E Tourgeman. (2011). DNA Fingerprinting Confirmation of Healthy Livebirth Following PGS Results: Indicating Trisomy 3 of Paternal Origin and Likely Embryo Mosaicism. Fertility and Sterility. 95(4). S11–S11. 2 indexed citations
7.
Langfelder-Schwind, E., Edward M. Kloza, Elaine A. Sugarman, et al.. (2005). Cystic Fibrosis Prenatal Screening in Genetic Counseling Practice: Recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling. 14(1). 1–15. 20 indexed citations
8.
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
9.
Laurino, Mercy, Robin L. Bennett, L. Baumeister, et al.. (2005). Genetic Evaluation and Counseling of Couples with Recurrent Miscarriage: Recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling. 14(3). 165–181. 40 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. 4 indexed citations
11.
Bennett, Robin L., B. Pettersen, Kristin B. Niendorf, & Rebecca Rae Anderson. (2003). Developing Standard Recommendations (Guidelines) for Genetic Counseling Practice: A Process of the National Society of Genetic Counselors. Journal of Genetic Counseling. 12(4). 287–295. 1 indexed citations
12.
Pauli, Richard M. & B. Pettersen. (1986). Is reserpine a human teratogen?. Journal of Medical Genetics. 23(3). 267–268. 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.

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