Lois J. Starr

1.3k total citations
30 papers, 720 citations indexed

About

Lois J. Starr is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Lois J. Starr has authored 30 papers receiving a total of 720 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 10 papers in Molecular Biology and 9 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Lois J. Starr's work include Connective tissue disorders research (9 papers), Genomic variations and chromosomal abnormalities (9 papers) and Aortic Disease and Treatment Approaches (4 papers). Lois J. Starr is often cited by papers focused on Connective tissue disorders research (9 papers), Genomic variations and chromosomal abnormalities (9 papers) and Aortic Disease and Treatment Approaches (4 papers). Lois J. Starr collaborates with scholars based in United States, South Africa and Romania. Lois J. Starr's co-authors include Anji T. Yetman, Júlio Cabrera, Elaine Wang, Wentzel C.A. Gelderblom, Ronald T. Riley, T. W. Sadler, Walter F. O. Marasas, Carolina Martínez, Katherine Hendricks and M. Cameron Sullards and has published in prestigious journals such as The Journal of Cell Biology, PEDIATRICS and Journal of Nutrition.

In The Last Decade

Lois J. Starr

29 papers receiving 682 citations

Peers

Lois J. Starr
Ana da Silva Lédo Brazil
Philip A. I. Guthrie United Kingdom
Stacey A. Missmer United States
Juha‐Pekka Pursiheimo Finland
Jingbo Zhao United States
Lili Cheng China
Toshiyuki Mano Japan
Catalina Sanz Spain
Nicola Antonio Martino Italy
Hengmi Cui China
Ana da Silva Lédo Brazil
Lois J. Starr
Citations per year, relative to Lois J. Starr Lois J. Starr (= 1×) peers Ana da Silva Lédo

Countries citing papers authored by Lois J. Starr

Since Specialization
Citations

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

Fields of papers citing papers by Lois J. Starr

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lois J. Starr. 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 Lois J. Starr. The network helps show where Lois J. Starr may publish in the future.

Co-authorship network of co-authors of Lois J. Starr

This figure shows the co-authorship network connecting the top 25 collaborators of Lois J. Starr. A scholar is included among the top collaborators of Lois J. Starr 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 Lois J. Starr. Lois J. Starr 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.
Lin, Angela E., et al.. (2024). The Myhre Syndrome Foundation as a global modern support group: The business of rare. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 196(4). e32104–e32104. 1 indexed citations
2.
Cummings, Christopher T. & Lois J. Starr. (2022). Biallelic GTF2IRD1 variants in brothers with profound neurodevelopmental disorder: A possible novel disorder involving a critical gene for Williams syndrome. American Journal of Medical Genetics Part A. 191(2). 332–337. 1 indexed citations
3.
Starr, Lois J., et al.. (2021). Second reported individual with a partial STAG2 deletion: middle interhemispheric variant holoprosencephaly in STAG2-related cohesinopathy. Clinical Dysmorphology. 30(3). 159–163. 2 indexed citations
4.
Yetman, Anji T., et al.. (2020). Vascular dissection in women with Turner syndrome. International Journal of Cardiology. 325. 127–131. 7 indexed citations
5.
Yetman, Anji T., et al.. (2020). The QT Interval in Patients With the Turner Syndrome. The American Journal of Cardiology. 140. 118–121. 7 indexed citations
6.
Starr, Lois J., et al.. (2019). Utilization of echocardiography in Ehlers‐Danlos syndrome. Congenital Heart Disease. 14(5). 864–867. 13 indexed citations
7.
Starr, Lois J., Jürgen W. Spranger, Vamshi K. Rao, Richard E. Lutz, & Anji T. Yetman. (2019). PIGQ glycosylphosphatidylinositol‐anchored protein deficiency: Characterizing the phenotype. American Journal of Medical Genetics Part A. 179(7). 1270–1275. 9 indexed citations
8.
Yetman, Anji T., et al.. (2018). Clinical and Echocardiographic Prevalence and Detection of Congenital and Acquired Cardiac Abnormalities in Girls and Women with the Turner Syndrome. The American Journal of Cardiology. 122(2). 327–330. 13 indexed citations
9.
Yetman, Anji T. & Lois J. Starr. (2018). Newly described recessive MYH11 disorder with clinical overlap of Multisystemic smooth muscle dysfunction and Megacystis microcolon hypoperistalsis syndromes. American Journal of Medical Genetics Part A. 176(4). 1011–1014. 23 indexed citations
10.
Weaver, Meaghann S., et al.. (2018). Eliciting Narratives to Inform Care for Infants With Trisomy 18. PEDIATRICS. 142(4). 6 indexed citations
11.
Sanmann, Jennifer N., Diane L. Pickering, Jadd M. Stevens, et al.. (2015). Assessing the utility of confirmatory studies following identification of large-scale genomic imbalances by microarray. Genetics in Medicine. 17(11). 875–879. 5 indexed citations
12.
Starr, Lois J., Dorothy K. Grange, Jeffrey W. Delaney, et al.. (2015). Myhre syndrome: Clinical features and restrictive cardiopulmonary complications. American Journal of Medical Genetics Part A. 167(12). 2893–2901. 27 indexed citations
13.
Zárate, Yuri A., Katherine A. Bosanko, Elizabeth Bhoj, et al.. (2015). Phenotypic modifications of patients with full chromosome aneuploidies and concurrent suspected or confirmed second diagnoses. American Journal of Medical Genetics Part A. 167(9). 2168–2175. 4 indexed citations
14.
Starr, Lois J., Edward J. Truemper, Diane L. Pickering, Warren G. Sanger, & Ann Haskins Olney. (2014). Duplication of 20qter and deletion of 20pter due to paternal pericentric inversion: Patient report and review of 20qter duplications. American Journal of Medical Genetics Part A. 164(8). 2020–2024. 13 indexed citations
15.
Starr, Lois J., et al.. (2014). Occurrence of nephroblastomatosis with dup(18)(q11.2‐q23) implicates trisomy 18 tumor screening protocol in select patients with 18q duplication. American Journal of Medical Genetics Part A. 164(4). 1079–1082. 4 indexed citations
16.
Kanev, I., W. N. Mei, Akira Mizuno, et al.. (2013). SEARCHING FOR ELECTRICAL PROPERTIES, PHENOMENA AND MECHANISMS IN THE CONSTRUCTION AND FUNCTION OF CHROMOSOMES. Computational and Structural Biotechnology Journal. 6(7). e201303007–e201303007. 3 indexed citations
17.
Sanmann, Jennifer N., Lois J. Starr, Diane L. Pickering, et al.. (2012). Characterization of six novel patients with MECP2 duplications due to unbalanced rearrangements of the X chromosome. American Journal of Medical Genetics Part A. 158A(6). 1285–1291. 19 indexed citations
18.
Schaefer, G. Bradley, et al.. (2010). Array Comparative Genomic Hybridization Findings in a Cohort Referred for an Autism Evaluation. Journal of Child Neurology. 25(12). 1498–1503. 22 indexed citations
19.
20.
Tamura, Richard N., Carla Rozzo, Lois J. Starr, et al.. (1990). 上皮性インテグリンα 6 β 4 α 6 とβ 4 の変異体型の完全な一次構造. The Journal of Cell Biology. 111(4). 1593–1604. 2 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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