Jennifer E. Posey

9.5k total citations
61 papers, 813 citations indexed

About

Jennifer E. Posey is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Jennifer E. Posey has authored 61 papers receiving a total of 813 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Genetics, 31 papers in Molecular Biology and 7 papers in Surgery. Recurrent topics in Jennifer E. Posey's work include Genomic variations and chromosomal abnormalities (22 papers), Genomics and Rare Diseases (21 papers) and RNA modifications and cancer (8 papers). Jennifer E. Posey is often cited by papers focused on Genomic variations and chromosomal abnormalities (22 papers), Genomics and Rare Diseases (21 papers) and RNA modifications and cancer (8 papers). Jennifer E. Posey collaborates with scholars based in United States, Kuwait and Türkiye. Jennifer E. Posey's co-authors include James R. Lupski, Shalini N. Jhangiani, Zeynep Coban‐Akdemir, Richard A. Gibbs, Michael F. Wangler, Shinya Yamamoto, Monte Westerfield, Philip Hieter, Hugo J. Bellen and Philippe M. Campeau and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and Journal of the American College of Cardiology.

In The Last Decade

Jennifer E. Posey

57 papers receiving 807 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jennifer E. Posey United States	16	481	394	83	58	54	61	813
Nisha Patel Saudi Arabia	17	428 0.9×	267 0.7×	60 0.7×	52 0.9×	69 1.3×	39	727
Pamela Magini Italy	16	347 0.7×	349 0.9×	119 1.4×	45 0.8×	27 0.5×	38	717
Khushnooda Ramzan Saudi Arabia	18	644 1.3×	320 0.8×	84 1.0×	59 1.0×	112 2.1×	79	1.2k
Erica Andersen United States	16	612 1.3×	773 2.0×	97 1.2×	65 1.1×	75 1.4×	28	1.5k
Pauline Terhal Netherlands	18	574 1.2×	632 1.6×	59 0.7×	31 0.5×	79 1.5×	28	1.0k
Bryn D. Webb United States	13	588 1.2×	212 0.5×	60 0.7×	34 0.6×	59 1.1×	35	896
Jean‐Pierre Desvignes France	17	603 1.3×	324 0.8×	72 0.9×	99 1.7×	96 1.8×	31	1.0k
Davut Pehli̇van United States	17	656 1.4×	508 1.3×	74 0.9×	117 2.0×	77 1.4×	62	1.1k
Donna M. Muzny United States	15	551 1.1×	456 1.2×	40 0.5×	53 0.9×	52 1.0×	20	854
Gülen Eda Ütine Türkiye	14	367 0.8×	373 0.9×	28 0.3×	52 0.9×	54 1.0×	114	715

Countries citing papers authored by Jennifer E. Posey

Since Specialization

Citations

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

Fields of papers citing papers by Jennifer E. Posey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jennifer E. Posey. 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 Jennifer E. Posey. The network helps show where Jennifer E. Posey may publish in the future.

Co-authorship network of co-authors of Jennifer E. Posey

This figure shows the co-authorship network connecting the top 25 collaborators of Jennifer E. Posey. A scholar is included among the top collaborators of Jennifer E. Posey 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 Jennifer E. Posey. Jennifer E. Posey 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

Pehli̇van, Davut, Richard A. Gibbs, Osman Uğur Sezerman, et al.. (2024). Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders. BMC Medical Genomics. 17(1). 85–85.

Fatih, Jawid M., Angad Jolly, Moez Dawood, et al.. (2024). NODAL variants are associated with a continuum of laterality defects from simple D-transposition of the great arteries to heterotaxy. Genome Medicine. 16(1). 53–53. 3 indexed citations

Posey, Jennifer E., et al.. (2024). Human embryonic genetic mosaicism and its effects on development and disease. Nature Reviews Genetics. 25(10). 698–714. 11 indexed citations

Sobreira, Nara, Sean J. Griffith, Corina Antonescu, et al.. (2023). P669: VariantMatcher: A tool to enable connections amongst individuals with interest in a specific variant. SHILAP Revista de lepidopterología. 1(1). 100734–100734. 1 indexed citations

Marafi, Dana, Ruizhi Duan, Shalini N. Jhangiani, et al.. (2023). Novel LSS variants in alopecia and intellectual disability syndrome: New case report and clinical spectrum of LSS ‐related rare disease traits. Clinical Genetics. 104(3). 344–349.

Du, Haowei, Angad Jolly, Christopher M. Grochowski, et al.. (2023). HMZDupFinder: a robust computational approach for detecting intragenic homozygous duplications from exome sequencing data. Nucleic Acids Research. 52(4). e18–e18. 2 indexed citations

Eldomery, Mohammad K., Lorraine Potocki, Dana Marafi, et al.. (2022). De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome. American Journal of Medical Genetics Part A. 188(8). 2360–2366. 3 indexed citations

Calame, Daniel G., Tadahiro Mitani, Jawid M. Fatih, et al.. (2022). Novel RETREG1 (FAM134B) founder allele is linked to HSAN2B and renal disease in a Turkish family. American Journal of Medical Genetics Part A. 188(7). 2153–2161. 3 indexed citations

Calame, Daniel G., Jawid M. Fatih, Isabella Herman, et al.. (2021). Deep clinicopathological phenotyping identifies a previously unrecognized pathogenic EMD splice variant. Annals of Clinical and Translational Neurology. 8(10). 2052–2058.

10.

Rosenfeld, Jill A., Lauren Westerfield, Amanda Gerard, et al.. (2021). Clinical characterization of individuals with the distal 1q21.1 microdeletion. American Journal of Medical Genetics Part A. 185(5). 1388–1398. 13 indexed citations

11.

Tosur, Mustafa, Claudia Soler‐Alfonso, Michael M. Khayat, et al.. (2021). Exome sequencing in children with clinically suspected maturity‐onset diabetes of the young. Pediatric Diabetes. 22(7). 960–968. 5 indexed citations

12.

Herman, Isabella, Angad Jolly, Haowei Du, et al.. (2021). Quantitative dissection of multilocus pathogenic variation in an Egyptian infant with severe neurodevelopmental disorder resulting from multiple molecular diagnoses. American Journal of Medical Genetics Part A. 188(3). 735–750. 7 indexed citations

13.

Calame, Daniel G., Isabella Herman, Jawid M. Fatih, et al.. (2021). Risk of sudden cardiac death in EXOSC5‐related disease. American Journal of Medical Genetics Part A. 185(8). 2532–2540. 10 indexed citations

14.

Calame, Daniel G., Jawid M. Fatih, Isabella Herman, et al.. (2021). Biallelic Pathogenic Variants in TNNT3 Associated With Congenital Myopathy. Neurology Genetics. 7(3). e589–e589. 9 indexed citations

15.

Wild, K. Taylor, Elizabeth Bhoj, Haowei Du, et al.. (2020). Congenital diaphragmatic hernia as a prominent feature of a SPECC1L‐related syndrome. American Journal of Medical Genetics Part A. 182(12). 2919–2925. 6 indexed citations

16.

Chen, Shan, Mahim Jain, Shalini N. Jhangiani, et al.. (2019). Genetic Burden Contributing to Extremely Low or High Bone Mineral Density in a Senior Male Population From the Osteoporotic Fractures in Men Study (MrOS). JBMR Plus. 4(3). e10335–e10335. 1 indexed citations

17.

Batzir, Nurit Assia, Jennifer E. Posey, Xiaofei Song, et al.. (2019). Phenotypic expansion of POGZ‐related intellectual disability syndrome (White‐Sutton syndrome). American Journal of Medical Genetics Part A. 182(1). 38–52. 30 indexed citations

18.

Boone, Philip M., Bo Yuan, Shen Gu, et al.. (2015). Hutterite‐type cataract maps to chromosome 6p21.32‐p21.31, cosegregates with a homozygous mutation in LEMD2, and is associated with sudden cardiac death. Molecular Genetics & Genomic Medicine. 4(1). 77–94. 25 indexed citations

19.

Posey, Jennifer E., Lindsay C. Burrage, Marcus J. Miller, et al.. (2014). Lysinuric protein intolerance presenting with multiple fractures. Molecular Genetics and Metabolism Reports. 1. 176–183. 18 indexed citations

20.

Lu, Ping, Jennifer E. Posey, & David B. Roth. (2008). Understanding how the V(D)J recombinase catalyzes transesterification: distinctions between DNA cleavage and transposition. Nucleic Acids Research. 36(9). 2864–2873. 6 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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