Kristin Petras

1.0k total citations
7 papers, 306 citations indexed

About

Kristin Petras is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Kristin Petras has authored 7 papers receiving a total of 306 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Oncology. Recurrent topics in Kristin Petras's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Hematopoietic Stem Cell Transplantation (2 papers). Kristin Petras is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Hematopoietic Stem Cell Transplantation (2 papers). Kristin Petras collaborates with scholars based in United States, Brazil and Australia. Kristin Petras's co-authors include William B. Dobyns, Soma Das, Mitsuhiro Kato, Soma Das, Yukio Sawaishi, Richard J. Leventer, Eden Haverfield, Heather L. Ward, Daniela T. Pilz and Christa Lese Martin and has published in prestigious journals such as Blood, Neurology and Human Mutation.

In The Last Decade

Kristin Petras

7 papers receiving 289 citations

Peers

Countries citing papers authored by Kristin Petras

Since Specialization

Citations

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

Fields of papers citing papers by Kristin Petras

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kristin Petras

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

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Molecular and Clinicopathologic Characterization of HER2-overexpressed Squamous Cell Carcinoma of the Cervix 2024 ·International Journal of Gynecological Pathology ·(unknown), (unknown), (unknown), (unknown), Raavi Gupta, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Kristin Petras, (unknown), Carrie Fitzpatrick, Jeremy P. Segal, Peng Wang, Ricardo R. Lastra	2
2	Feasibility and limitations of cultured skin fibroblasts for germline genetic testing in hematologic disorders 2022 ·Human Mutation ·(unknown), (unknown), Kristin Petras, Kelly Arndt, (unknown), Pankhuri Wanjari, (unknown), David M. Montes, James McElherne, (unknown), (unknown), Soma Das, Lucy A. Godley, Jeremy Segal, Daniela del Gaudio, Carrie Fitzpatrick, Jane E. Churpek	17
3	Assessing the Feasibility and Limitations of Cultured Skin Fibroblasts for Germline Genetic Testing in Hematologic Disorders 2020 ·Blood ·(unknown), (unknown), Kristin Petras, Kelly Arndt, (unknown), Pankhuri Wanjari, (unknown), David M. Montes, Soma Das, Lucy A. Godley, Jeremy Segal, Daniela del Gaudio, Carrie Fitzpatrick, Jane E. Churpek	2
4	Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia 2008 ·European Journal of Human Genetics ·Eden Haverfield, (unknown), Kristin Petras, William B. Dobyns, Soma Das	51
5	Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1–p23.1, 4q21.21–q22.1, 6q26–q27, and 21q2 2008 ·American Journal of Medical Genetics Part A ·William B. Dobyns, Ghayda Mirzaa, Susan L. Christian, Kristin Petras, (unknown), Gary Clark, Cynthia J. Curry, Donna M. McDonald‐McGinn, Līvija Medne, Elaine H. Zackai, Julie Parsons, Dina J. Zand, Fuki M. Hisama, Christopher A. Walsh, Richard J. Leventer, Alastair J. Martin, Marzena Gajęcka, Lisa G. Shaffer	74
6	Polyalanine expansion of ARX associated with cryptogenic West syndrome 2003 ·Neurology ·Mitsuhiro Kato, Soma Das, Kristin Petras, Yukio Sawaishi, William B. Dobyns	70
7	Clinical and molecular basis of classical lissencephaly: Mutations in theLIS1 gene (PAFAH1B1) 2001 ·Human Mutation ·Carlos Cardoso, Richard J. Leventer, James J. Dowling, Heather L. Ward, (unknown), Kristin Petras, (unknown), (unknown), Soma Das, Christa Lese Martin, Daniela T. Pilz, William B. Dobyns, David H. Ledbetter	90

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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