Aline Petrin

1.3k total citations
12 papers, 310 citations indexed

About

Aline Petrin is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Aline Petrin has authored 12 papers receiving a total of 310 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Aline Petrin's work include Cleft Lip and Palate Research (8 papers), Craniofacial Disorders and Treatments (7 papers) and Genomic variations and chromosomal abnormalities (4 papers). Aline Petrin is often cited by papers focused on Cleft Lip and Palate Research (8 papers), Craniofacial Disorders and Treatments (7 papers) and Genomic variations and chromosomal abnormalities (4 papers). Aline Petrin collaborates with scholars based in United States, Brazil and Canada. Aline Petrin's co-authors include Jeffrey C. Murray, Antônio Richieri‐Costa, JC Murray, A. Richieri‐Costa, Natalia Freitas Rossi, Maria Teresa Vieira Sanseverino, Luciana Paula Maximino, Célia Maria Giacheti, Dagma Venturini Marques Abramides and Têmis Maria Félix and has published in prestigious journals such as SHILAP Revista de lepidopterología, Genetics and The American Journal of Human Genetics.

In The Last Decade

Aline Petrin

12 papers receiving 307 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aline Petrin United States 9 229 154 53 35 27 12 310
Jeffrey C. Murray United States 14 231 1.0× 209 1.4× 36 0.7× 43 1.2× 33 1.2× 21 461
Constance T. R. M. Stumpel Netherlands 12 210 0.9× 166 1.1× 23 0.4× 33 0.9× 27 1.0× 32 348
Erica H. Gerkes Netherlands 10 203 0.9× 221 1.4× 43 0.8× 37 1.1× 22 0.8× 14 386
Elga Fabia Belligni Italy 9 179 0.8× 114 0.7× 15 0.3× 46 1.3× 23 0.9× 16 256
Florencia Giliberto Argentina 11 68 0.3× 312 2.0× 49 0.9× 29 0.8× 11 0.4× 28 409
Valerie Drasinover Israel 8 214 0.9× 172 1.1× 35 0.7× 19 0.5× 114 4.2× 8 374
Stefanie Birnbaum Germany 10 281 1.2× 198 1.3× 45 0.8× 39 1.1× 23 0.9× 12 341
Mauro Pierluigi Italy 14 379 1.7× 248 1.6× 43 0.8× 33 0.9× 23 0.9× 26 496
Chloe Stutterd Australia 9 135 0.6× 109 0.7× 14 0.3× 20 0.6× 13 0.5× 18 283
Aušra Matulevičienė Lithuania 10 216 0.9× 222 1.4× 38 0.7× 19 0.5× 14 0.5× 24 348

Countries citing papers authored by Aline Petrin

Since Specialization
Citations

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

Fields of papers citing papers by Aline Petrin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aline Petrin

This figure shows the co-authorship network connecting the top 25 collaborators of Aline Petrin. A scholar is included among the top collaborators of Aline Petrin 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 Aline Petrin. Aline Petrin 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.
Qian, Fang, et al.. (2024). DNA Methylation Effects on Van der Woude Syndrome Phenotypic Variability. The Cleft Palate-Craniofacial Journal. 62(10). 1641–1650. 1 indexed citations
2.
Petrin, Aline, Erliang Zeng, Mary Ann Thomas, et al.. (2023). DNA methylation differences in monozygotic twins with Van der Woude syndrome. SHILAP Revista de lepidopterología. 4. 2 indexed citations
3.
Darbro, Benjamin W., Aline Petrin, Jennifer Standley, et al.. (2017). Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in Humans. Genetics. 208(1). 283–296. 19 indexed citations
4.
Liu, Huan, Tamara Busch, Steven Eliason, et al.. (2016). Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate. Birth Defects Research. 109(1). 27–37. 33 indexed citations
5.
Butali, Azeez, Satoshi Suzuki, Margaret E. Cooper, et al.. (2013). Replication of Genome Wide Association Identified Candidate Genes Confirm the Role of Common and Rare Variants inPAX7andVAX1in the Etiology of Nonsyndromic CL(P). American Journal of Medical Genetics Part A. 161(5). 965–972. 46 indexed citations
6.
Kokitsu‐Nakata, Nancy Mizue, Aline Petrin, Jason Heard, et al.. (2012). Analysis of MLL2 gene in the first Brazilian family with Kabuki syndrome. American Journal of Medical Genetics Part A. 158A(8). 2003–2008. 13 indexed citations
7.
Jobling, Rebekah, et al.. (2011). Monozygotic twins with variable expression of Van der Woude Syndrome. American Journal of Medical Genetics Part A. 155(8). 2008–2010. 9 indexed citations
8.
Saadi, Irfan, Fowzan S. Alkuraya, Stephen S. Gisselbrecht, et al.. (2011). Deficiency of the Cytoskeletal Protein SPECC1L Leads to Oblique Facial Clefting. The American Journal of Human Genetics. 89(1). 44–55. 55 indexed citations
9.
Petrin, Aline, et al.. (2010). Clinical findings in patients with GLI2 mutations – phenotypic variability. Clinical Genetics. 81(1). 70–75. 48 indexed citations
10.
Petrin, Aline, Célia Maria Giacheti, Luciana Paula Maximino, et al.. (2010). Identification of a microdeletion at the 7q33‐q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case. American Journal of Medical Genetics Part A. 152A(12). 3164–3172. 51 indexed citations
11.
Félix, Têmis Maria, Aline Petrin, Maria Teresa Vieira Sanseverino, & Jeffrey C. Murray. (2010). Further characterization of microdeletion syndrome involving 2p15‐p16.1. American Journal of Medical Genetics Part A. 152A(10). 2604–2608. 25 indexed citations
12.
Petrin, Aline, Sandra Daack‐Hirsch, Jamie L’Heureux, & Jeffrey C. Murray. (2010). A Case of 3q29 Microdeletion Syndrome Involving Oral Cleft Inherited from a Nonaffected Mosaic Parent: Molecular Analysis and Ethical Implications. The Cleft Palate-Craniofacial Journal. 48(2). 222–230. 8 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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