Lori Dobson

555 total citations
20 papers, 186 citations indexed

About

Lori Dobson is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Surgery. According to data from OpenAlex, Lori Dobson has authored 20 papers receiving a total of 186 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Pediatrics, Perinatology and Child Health, 6 papers in Genetics and 4 papers in Surgery. Recurrent topics in Lori Dobson's work include Prenatal Screening and Diagnostics (16 papers), Fetal and Pediatric Neurological Disorders (7 papers) and Genomic variations and chromosomal abnormalities (5 papers). Lori Dobson is often cited by papers focused on Prenatal Screening and Diagnostics (16 papers), Fetal and Pediatric Neurological Disorders (7 papers) and Genomic variations and chromosomal abnormalities (5 papers). Lori Dobson collaborates with scholars based in United States and Poland. Lori Dobson's co-authors include Louise Wilkins‐Haug, Sarah E Little, Emily Reiff, Bryann Bromley, Rosemary Reiss, Andrea Lanes, Judy A. Estroff, Elizabeth S. Ginsburg, Omar Khwaja and Heather Mason‐Suares and has published in prestigious journals such as Blood, American Journal of Obstetrics and Gynecology and Clinical Chemistry.

In The Last Decade

Lori Dobson

20 papers receiving 183 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lori Dobson United States	7	158	63	47	39	34	20	186
Ida Charlotte Bay Lund Denmark	7	153 1.0×	76 1.2×	22 0.5×	36 0.9×	26 0.8×	16	185
Laurent Bidat France	10	262 1.7×	52 0.8×	93 2.0×	73 1.9×	45 1.3×	20	314
Jennifer Saucier United States	4	173 1.1×	97 1.5×	53 1.1×	34 0.9×	20 0.6×	5	222
Tanja Schlaikjær Hartwig Denmark	7	255 1.6×	85 1.3×	67 1.4×	40 1.0×	23 0.7×	14	281
Sarit Kahana Israel	8	207 1.3×	141 2.2×	49 1.0×	47 1.2×	60 1.8×	22	269
Junko Yotsumoto Japan	10	154 1.0×	58 0.9×	36 0.8×	51 1.3×	18 0.5×	18	242
Lucia Tului Italy	10	266 1.7×	91 1.4×	62 1.3×	31 0.8×	69 2.0×	16	304
Qiuyu Liu China	2	242 1.5×	87 1.4×	98 2.1×	25 0.6×	22 0.6×	4	256
Mindy Preston Dabell United States	5	359 2.3×	273 4.3×	38 0.8×	68 1.7×	56 1.6×	5	403

Countries citing papers authored by Lori Dobson

Since Specialization

Citations

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

Fields of papers citing papers by Lori Dobson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lori Dobson

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Dobson, Lori, Sean A. Horan, Michael Duyzend, et al.. (2025). Routine Prenatal cfDNA Screening for Autosomal Dominant Single-Gene Conditions. Clinical Chemistry. 71(1). 129–140. 3 indexed citations

Cirino, Allison L., et al.. (2023). Reproductive decision‐making and the utilization of preimplantation genetic testing among individuals with inherited aortic or vascular disease. Journal of Genetic Counseling. 33(3). 592–604. 4 indexed citations

Dobson, Lori, et al.. (2023). Single gene non‐invasive prenatal screening for autosomal dominant conditions in a high‐risk cohort. Prenatal Diagnosis. 43(9). 1110–1119. 7 indexed citations

Dobson, Lori, et al.. (2023). Postnatal genetic testing on cord blood for prenatally identified high‐probability cases. Prenatal Diagnosis. 43(9). 1120–1131. 2 indexed citations

Lanes, Andrea, Kathryn J. Go, Lori Dobson, et al.. (2023). Multiple embryo manipulations in PGT-A cycles may result in inferior clinical outcomes. Reproductive BioMedicine Online. 48(2). 103619–103619. 7 indexed citations

Dobson, Lori, et al.. (2022). Use of preimplantation genetic testing for monogenic disorders and subsequent prenatal care and diagnostic testing. Prenatal Diagnosis. 42(8). 1022–1030. 3 indexed citations

Guseh, Stephanie, Louise Wilkins‐Haug, Anjali J. Kaimal, et al.. (2021). Utility of noninvasive genome-wide screening: a prospective cohort of obstetric patients undergoing diagnostic testing. Genetics in Medicine. 23(7). 1341–1348. 5 indexed citations

Lanes, Andrea, et al.. (2021). Blastocyst conversion rate and ploidy in patients with structural rearrangements. Journal of Assisted Reproduction and Genetics. 38(5). 1143–1151. 6 indexed citations

Reimers, Rebecca, Heather Mason‐Suares, Sarah E Little, et al.. (2018). When ultrasound anomalies are present: An estimation of the frequency of chromosome abnormalities not detected by cell‐free DNA aneuploidy screens. Prenatal Diagnosis. 38(4). 250–257. 13 indexed citations

10.

Reiss, Rosemary, et al.. (2017). Sex chromosome aneuploidy detection by noninvasive prenatal testing: helpful or hazardous?. Prenatal Diagnosis. 37(5). 515–520. 47 indexed citations

11.

Reiss, Rosemary, et al.. (2017). Sex Chromosome Aneuploidy Detection by Noninvasive Prenatal Testing: Helpful or Hazardous?. Obstetrical & Gynecological Survey. 72(10). 583–585. 2 indexed citations

12.

Reiff, Emily, Lori Dobson, Bryann Bromley, et al.. (2017). The influence of noninvasive prenatal testing on gestational age at time of abortion for aneuploidy. Prenatal Diagnosis. 37(7). 635–639. 6 indexed citations

13.

Reiff, Emily, Sarah E Little, Lori Dobson, Louise Wilkins‐Haug, & Bryann Bromley. (2016). What is the role of the 11- to 14-week ultrasound in women with negative cell-free DNA screening for aneuploidy?. Prenatal Diagnosis. 36(3). 260–265. 28 indexed citations

14.

Dobson, Lori, Emily Reiff, Sarah E Little, Louise Wilkins‐Haug, & Bryann Bromley. (2016). Patient choice and clinical outcomes following positive noninvasive prenatal screening for aneuploidy with cell-free DNA (cfDNA). Prenatal Diagnosis. 36(5). 456–462. 25 indexed citations

15.

Reimers, Rebecca, Lori Dobson, Rachel A. Pilliod, et al.. (2015). 598: Pregnancy outcomes for Trisomy 21 following NIPT, CVS, and amniocentesis. American Journal of Obstetrics and Gynecology. 214(1). S320–S320. 2 indexed citations

16.

Leeman, Kristen T., Lori Dobson, Meghan C. Towne, et al.. (2014). NPHP3 mutations are associated with neonatal onset multiorgan polycystic disease in two siblings. Journal of Perinatology. 34(5). 410–411. 5 indexed citations

17.

Dobson, Lori, et al.. (2013). Monozygotic Twins With Trisomy 21 and Partial Agenesis of the Corpus Callosum. Pediatric Neurology. 48(4). 314–316. 6 indexed citations

18.

Dobson, Lori, Carol E. Barnewolt, Donna Morash, Susan A. Connolly, & Judy A. Estroff. (2012). Human fetal sacrococcygeal extension or ‘tail’ in the second trimester: prenatal diagnosis, associated findings, and clinical outcome. Prenatal Diagnosis. 33(2). 134–140. 5 indexed citations

19.

Klein, Justin D., Christopher G. Turner, Lori Dobson, Harry P. Kozakewich, & Russell W. Jennings. (2011). Familial case of prenatally diagnosed intralobar and extralobar sequestrations with cystadenomatoid change. Journal of Pediatric Surgery. 46(2). e27–e31. 4 indexed citations

20.

Gazda, Hanna T., Michael Landowski, Christopher Buros, et al.. (2010). Array Comparative Genomic Hybridization of Ribosomal Protein Genes In Diamond-Blackfan Anemia Patients; Evidence for Three New DBA Genes, RPS8, RPS14 and RPL15, with Large Deletion or Duplication. Blood. 116(21). 1007–1007. 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.

Explore authors with similar magnitude of impact