Jodi D. Hoffman

2.0k total citations
33 papers, 654 citations indexed

About

Jodi D. Hoffman is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jodi D. Hoffman has authored 33 papers receiving a total of 654 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 11 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jodi D. Hoffman's work include Genomics and Rare Diseases (8 papers), Prenatal Screening and Diagnostics (8 papers) and BRCA gene mutations in cancer (4 papers). Jodi D. Hoffman is often cited by papers focused on Genomics and Rare Diseases (8 papers), Prenatal Screening and Diagnostics (8 papers) and BRCA gene mutations in cancer (4 papers). Jodi D. Hoffman collaborates with scholars based in United States, Canada and China. Jodi D. Hoffman's co-authors include Paige Kaplan, Kenneth Ward, Linda K. Nicholson, Katia Sol‐Church, Deborah L. Stabley, Karen W. Gripp, Elaine H. Zackai, Elizabeth A. Gilliam, Gloria Y. Yeh and Karen L. Ciprero and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and American Journal of Obstetrics and Gynecology.

In The Last Decade

Jodi D. Hoffman

31 papers receiving 629 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jodi D. Hoffman United States 18 365 215 119 74 67 33 654
Julie Neidich United States 17 231 0.6× 270 1.3× 148 1.2× 48 0.6× 33 0.5× 42 698
Lakshmi Mehta United States 16 348 1.0× 403 1.9× 86 0.7× 44 0.6× 35 0.5× 46 754
Siddharth Banka United Kingdom 18 480 1.3× 339 1.6× 69 0.6× 63 0.9× 125 1.9× 55 991
Tahsin Yakut Türkiye 15 191 0.5× 315 1.5× 174 1.5× 72 1.0× 61 0.9× 78 762
Periklis Makrythanasis Switzerland 18 278 0.8× 402 1.9× 59 0.5× 111 1.5× 54 0.8× 58 798
Sevilhan Artan Türkiye 18 187 0.5× 308 1.4× 104 0.9× 75 1.0× 43 0.6× 84 760
Nicole L. Hoppman United States 14 279 0.8× 279 1.3× 115 1.0× 38 0.5× 31 0.5× 62 704
Antoine Daunay France 15 206 0.6× 508 2.4× 133 1.1× 50 0.7× 83 1.2× 26 796
Carine Courtillot France 13 226 0.6× 206 1.0× 93 0.8× 30 0.4× 49 0.7× 32 774
Martha Salas United States 11 223 0.6× 458 2.1× 174 1.5× 41 0.6× 92 1.4× 18 745

Countries citing papers authored by Jodi D. Hoffman

Since Specialization
Citations

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

Fields of papers citing papers by Jodi D. Hoffman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jodi D. Hoffman. 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 Jodi D. Hoffman. The network helps show where Jodi D. Hoffman may publish in the future.

Co-authorship network of co-authors of Jodi D. Hoffman

This figure shows the co-authorship network connecting the top 25 collaborators of Jodi D. Hoffman. A scholar is included among the top collaborators of Jodi D. Hoffman 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 Jodi D. Hoffman. Jodi D. Hoffman 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.
Hoffman, Jodi D., et al.. (2020). Complexities of Clinical Genetics Consultation: An Interprofessional Clinical Skills Workshop. MedEdPORTAL. 16. 10869–10869. 3 indexed citations
2.
Torres, Raúl, Rotem Ben‐Shachar, Jodi D. Hoffman, et al.. (2020). Evaluation and classification of severity for 176 genes on an expanded carrier screening panel. Prenatal Diagnosis. 40(10). 1246–1257. 28 indexed citations
3.
Gilliam, Elizabeth A., Jodi D. Hoffman, & Gloria Y. Yeh. (2019). Urogenital and pelvic complications in the Ehlers‐Danlos syndromes and associated hypermobility spectrum disorders: A scoping review. Clinical Genetics. 97(1). 168–178. 26 indexed citations
4.
David, Karen L., Robert G. Best, Joshua L. Deignan, et al.. (2018). Patient re-contact after revision of genomic test results: points to consider—a statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 21(4). 769–771. 85 indexed citations
5.
Bhoj, Elizabeth, Dong Li, Margaret Harr, et al.. (2015). Expanding the SPECC1L mutation phenotypic spectrum to include Teebi hypertelorism syndrome. American Journal of Medical Genetics Part A. 167(11). 2497–2502. 17 indexed citations
6.
Hoffman, Jodi D., et al.. (2015). Three new families with recurrent male miscarriages and hypercoiled umbilical cord. Clinical Dysmorphology. 24(3). 128–131. 4 indexed citations
7.
Herman, Elizabeth, et al.. (2014). Knowledge, attitudes, and barriers to carrier screening for the Ashkenazi Jewish panel: a Florida experience. Journal of Community Genetics. 5(3). 223–231. 8 indexed citations
8.
Zielinski, Dina, Barak Markus, Mona A. Sheikh, et al.. (2014). OTX2 Duplication Is Implicated in Hemifacial Microsomia. PLoS ONE. 9(5). e96788–e96788. 35 indexed citations
9.
Schneider, Adele, Sachiko Nakagawa, Joel Charrow, et al.. (2009). Population‐based Tay‐Sachs screening among Ashkenazi Jewish young adults in the 21st century: Hexosaminidase a enzyme assay is essential for accurate testing. American Journal of Medical Genetics Part A. 149A(11). 2444–2447. 18 indexed citations
10.
Hoffman, Jodi D., Diana W. Bianchi, Lisa Sullivan, et al.. (2008). Down syndrome serum screening also identifies an increased risk for multicystic dysplastic kidney, two‐vessel cord, and hydrocele. Prenatal Diagnosis. 28(13). 1204–1208. 4 indexed citations
11.
Reis, Linda M., Rebecca C. Tyler, Omar Abdul‐Rahman, et al.. (2008). Mutation analysis of B3GALTL in Peters Plus syndrome. American Journal of Medical Genetics Part A. 146A(20). 2603–2610. 46 indexed citations
12.
Vora, Neeta L., et al.. (2008). 605: Prenatal findings in cases of familial and sporadic 22q11.2 deletion syndrome. American Journal of Obstetrics and Gynecology. 199(6). S174–S174.
13.
Segel, Reeval, Inga Peter, Laurie Demmer, et al.. (2006). The natural history of trisomy 12p. American Journal of Medical Genetics Part A. 140A(7). 695–703. 32 indexed citations
14.
Hoffman, Jodi D., et al.. (2006). Rhabdomyolysis in the Military: Recognizing Late-Onset Very Long-Chain Acyl Co-A Dehydrogenase Deficiency. Military Medicine. 171(7). 657–658. 20 indexed citations
15.
Gripp, Karen W., Deborah L. Stabley, Linda K. Nicholson, Jodi D. Hoffman, & Katia Sol‐Church. (2006). Somatic mosaicism for an HRAS mutation causes Costello syndrome. American Journal of Medical Genetics Part A. 140A(20). 2163–2169. 60 indexed citations
16.
Hoffman, Jodi D., et al.. (2005). Array based CGH and FISH fail to confirm duplication of 8p22-p23.1 in association with Kabuki syndrome. Journal of Medical Genetics. 42(1). 49–53. 20 indexed citations
17.
Hoffman, Jodi D., et al.. (2005). Familial variable expression of dilated cardiomyopathy in Alström syndrome: A report of four sibs. American Journal of Medical Genetics Part A. 135A(1). 96–98. 28 indexed citations
18.
Hoffman, Jodi D., Karen L. Ciprero, Kathleen E. Sullivan, et al.. (2005). Immune abnormalities are a frequent manifestation of Kabuki syndrome. American Journal of Medical Genetics Part A. 135A(3). 278–281. 60 indexed citations
19.
Hoffman, Jodi D. & Kenneth Ward. (1999). Genetic Factors in Preterm Delivery. Obstetrical & Gynecological Survey. 54(3). 203–210. 22 indexed citations
20.
Rafi, Mohammad A., et al.. (1994). Metachromatic leukodystrophy in the Navajo Indian population: A splice site mutation in intron 4 of the arylsulfatase a gene. Human Mutation. 4(3). 199–207. 21 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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