Lori Hoffner

1.5k citations
32 papers · 1.1k · h-index 17

Impact in

Papers in

    • Prenatal Screening and Diagnostics 15
    • Genetic Syndromes and Imprinting 8
    • Genomic variations and chromosomal abnormalities 6
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2

Lori Hoffner

32 papers receiving 1.0k citations

Peers

Lori Hoffner
Comparison fields: 5 of 55
  • Reproductive Medicine 212
  • Obstetrics and Gynecology 160
  • Pediatrics, Perinatology and Child Health 368
  • Public Health, Environmental and Occupational Health 411
  • Genetics 274
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Citations per year

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-authors

The 25 scholars most cited alongside Lori Hoffner, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Lori Hoffner Line = papers co-authored together Lori Hoffner links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 32 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Genetics and biology of human ovarian teratomas. I. Cytogenetic analysis and mechanism of origin.
1990138
2 2012130
3 200787
4 199282
5 200679
6 201270
7 201168
8 200560
9 199643
10 199439
11 201137
12 200232
13 200729
14 201424
15 200724
16
Simultaneous detection of imprinted gene expression (p57(KIP2)) and molecular cytogenetics (FICTION) in the evaluation of molar pregnancies.
201023
17 199820
18 201812
19 199612
20
Squamous cell carcinoma in situ arising in an ovarian mature cystic teratoma. Report of one case with histopathologic, cytogenetic, and flow cytometric DNA content analysis.
199111

About Lori Hoffner

Lori Hoffner is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Public Health, Environmental and Occupational Health, Molecular Biology and Surgery, having authored 32 papers that have together received 1.1k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (15 papers), Gestational Trophoblastic Disease Studies (13 papers), Genetic Syndromes and Imprinting (8 papers), Genomic variations and chromosomal abnormalities (6 papers), Ovarian cancer diagnosis and treatment (2 papers), Renal and related cancers (2 papers), Tumors and Oncological Cases (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Reproductive Medicine (212 citations), Obstetrics and Gynecology (160 citations), Pediatrics, Perinatology and Child Health (368 citations), Public Health, Environmental and Occupational Health (411 citations) and Genetics (274 citations). Lori Hoffner has collaborated with scholars based in United States, Hong Kong and Canada. Frequent co-authors include Urvashi Surti, R E Ferrell, Arnab Chakravarti, Trevor Macpherson, Aravinda Chakravarti, Ranjan Deka, Aleksandar Rajkovic, Mirka W. Jones, Megan McGuire and Alexander N. Yatsenko. Their work appears in journals such as Placenta, Journal of Medical Genetics, Prenatal Diagnosis, Cytogenetic and Genome Research and Genomics.

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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