Lori Hoffner

1.4k total citations
31 papers, 1.0k citations indexed

About

Lori Hoffner is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Lori Hoffner has authored 31 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 19 papers in Pediatrics, Perinatology and Child Health and 13 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Lori Hoffner's work include Prenatal Screening and Diagnostics (19 papers), Genetic Syndromes and Imprinting (12 papers) and Gestational Trophoblastic Disease Studies (12 papers). Lori Hoffner is often cited by papers focused on Prenatal Screening and Diagnostics (19 papers), Genetic Syndromes and Imprinting (12 papers) and Gestational Trophoblastic Disease Studies (12 papers). Lori Hoffner collaborates with scholars based in United States, Canada and Hong Kong. Lori Hoffner's co-authors include Urvashi Surti, R E Ferrell, Arnab Chakravarti, Trevor Macpherson, Aleksandar Rajkovic, Aravinda Chakravarti, Ranjan Deka, Mirka W. Jones, Alexander N. Yatsenko and Megan McGuire and has published in prestigious journals such as PLoS ONE, Fertility and Sterility and Human Pathology.

In The Last Decade

Lori Hoffner

31 papers receiving 979 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lori Hoffner United States 17 442 416 315 242 237 31 1.0k
F Flam Sweden 16 445 1.0× 319 0.8× 397 1.3× 482 2.0× 110 0.5× 50 1.0k
Ashutosh Halder India 16 243 0.5× 111 0.3× 166 0.5× 194 0.8× 110 0.5× 84 684
Michal Daniely Israel 12 269 0.6× 126 0.3× 225 0.7× 126 0.5× 44 0.2× 15 585
Krishna K. Yelavarthi United States 12 97 0.2× 191 0.5× 90 0.3× 134 0.6× 104 0.4× 13 957
Estrid Stæhr Hansen Denmark 19 148 0.3× 215 0.5× 70 0.2× 44 0.2× 869 3.7× 47 1.3k
Anthony T. Gordon United Kingdom 13 470 1.1× 157 0.4× 309 1.0× 297 1.2× 38 0.2× 19 878
I L Sargent United Kingdom 18 364 0.8× 351 0.8× 64 0.2× 334 1.4× 261 1.1× 38 1.2k
Seiryu Kamoi Japan 12 67 0.2× 57 0.1× 73 0.2× 136 0.6× 405 1.7× 33 745
D E Rooney United Kingdom 10 243 0.5× 72 0.2× 291 0.9× 245 1.0× 24 0.1× 14 631
S. Kertschanska Germany 12 249 0.6× 84 0.2× 47 0.1× 91 0.4× 45 0.2× 16 641

Countries citing papers authored by Lori Hoffner

Since Specialization
Citations

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

Fields of papers citing papers by Lori Hoffner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lori Hoffner

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

All Works

20 of 20 papers shown
1.
Allias, Fabienne, Lori Hoffner, Touria Hajri, et al.. (2020). A novel NLRP7 protein-truncating mutation associated with discordant and divergent p57 immunostaining in diploid biparental and triploid digynic moles. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 477(2). 309–315. 9 indexed citations
2.
Hu, Jie, Zhishuo Ou, Urvashi Surti, et al.. (2020). Four children with postnatally diagnosed mosaic trisomy 12: Clinical features, literature review, and current diagnostic capabilities of genetic testing. American Journal of Medical Genetics Part A. 182(4). 813–822. 6 indexed citations
3.
Mohan, K. Naga, Ye Cao, Sau Wai Cheung, et al.. (2018). Phenotypic association of 15q11.2 CNVs of the region of breakpoints 1–2 (BP1–BP2) in a large cohort of samples referred for genetic diagnosis. Journal of Human Genetics. 64(3). 253–255. 7 indexed citations
4.
Surti, Urvashi, Svetlana A. Yatsenko, Jie Hu, et al.. (2017). Maternal GRB10 microdeletion is a novel cause of cystic placenta: Spectrum of genomic changes in the etiology of enlarged cystic placenta. Placenta. 57. 33–41. 8 indexed citations
5.
Hoffner, Lori & Urvashi Surti. (2012). The genetics of gestational trophoblastic disease: a rare complication of pregnancy. Cancer Genetics. 205(3). 63–77. 67 indexed citations
6.
Liao, Jun, Malini Sathanoori, Svetlana A. Yatsenko, et al.. (2012). Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype. Prenatal Diagnosis. 32(12). 1166–1169. 1 indexed citations
7.
McGuire, Megan, Alexander N. Yatsenko, Lori Hoffner, et al.. (2012). Whole Exome Sequencing in a Random Sample of North American Women with Leiomyomas Identifies MED12 Mutations in Majority of Uterine Leiomyomas. PLoS ONE. 7(3). e33251–e33251. 123 indexed citations
8.
Wakim, Anthony N., et al.. (2011). Complex X chromosome rearrangement delineated by array comparative genome hybridization in a woman with premature ovarian insufficiency. Fertility and Sterility. 95(7). 2433.e9–2433.e15. 9 indexed citations
9.
Cajaiba, Mariana M., Selma F. Witchel, Suneeta Madan‐Khetarpal, et al.. (2011). Prenatal diagnosis of trisomy 6 rescue resulting in paternal UPD6 with novel placental findings. American Journal of Medical Genetics Part A. 155(8). 1996–2002. 6 indexed citations
10.
Slim, Rima, Asangla Ao, Urvashi Surti, et al.. (2011). Recurrent triploid and dispermic conceptions in patients with NLRP7 mutations. Placenta. 32(5). 409–412. 34 indexed citations
11.
12.
Surti, Urvashi, et al.. (2007). The origin of trisomy 22: Evidence for acrocentric chromosome‐specific patterns of nondisjunction. American Journal of Medical Genetics Part A. 143A(19). 2249–2255. 29 indexed citations
13.
Chan, E. Ricky, Andrew Collins, LuAnn Judis, et al.. (2007). The origin of trisomy 13. American Journal of Medical Genetics Part A. 143A(19). 2242–2248. 23 indexed citations
14.
Surti, Urvashi, et al.. (2006). Persistent Gestational Trophoblastic Disease After an Androgenetic/Biparental Fetal Chimera. International Journal of Gynecological Pathology. 25(4). 366–372. 79 indexed citations
15.
Surti, Urvashi, et al.. (2005). Twin pregnancy with a chimeric androgenetic and biparental placenta in one twin displaying placental mesenchymal dysplasia phenotype. Prenatal Diagnosis. 25(11). 1048–1056. 58 indexed citations
16.
Fan, Jian‐Bing, Urvashi Surti, Patricia Taillon‐Miller, et al.. (2002). Paternal Origins of Complete Hydatidiform Moles Proven by Whole Genome Single-Nucleotide Polymorphism Haplotyping. Genomics. 79(1). 58–62. 30 indexed citations
17.
Rao, Uma N. M., Urvashi Surti, Lori Hoffner, & Kenneth Yaw. (1996). Cytogenetic and histologic correlation of peripheral nerve sheath tumors of soft tissue. Cancer Genetics and Cytogenetics. 88(1). 17–25. 40 indexed citations
18.
Hoffner, Lori, Ranjan Deka, Aravinda Chakravarti, & Urvashi Surti. (1994). Cytogenetics and origins of pediatric germ cell tumors. Cancer Genetics and Cytogenetics. 74(1). 54–58. 29 indexed citations
19.
Hoffner, Lori, Susan Shen‐Schwarz, Ranjan Deka, Aravinda Chakravarti, & Urvashi Surti. (1992). Genetics and biology of human ovarian teratomas. Cancer Genetics and Cytogenetics. 62(1). 58–65. 73 indexed citations
20.
Surti, Urvashi, Lori Hoffner, Arnab Chakravarti, & R E Ferrell. (1990). Genetics and biology of human ovarian teratomas. I. Cytogenetic analysis and mechanism of origin.. PubMed. 47(4). 635–43. 129 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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