Sarah L. Nolin

2.7k total citations
44 papers, 1.6k citations indexed

About

Sarah L. Nolin is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Sarah L. Nolin has authored 44 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Genetics, 26 papers in Cognitive Neuroscience and 16 papers in Molecular Biology. Recurrent topics in Sarah L. Nolin's work include Genetics and Neurodevelopmental Disorders (39 papers), Genomic variations and chromosomal abnormalities (28 papers) and Autism Spectrum Disorder Research (26 papers). Sarah L. Nolin is often cited by papers focused on Genetics and Neurodevelopmental Disorders (39 papers), Genomic variations and chromosomal abnormalities (28 papers) and Autism Spectrum Disorder Research (26 papers). Sarah L. Nolin collaborates with scholars based in United States, United Kingdom and Australia. Sarah L. Nolin's co-authors include Carl Dobkin, Anne Glicksman, George E. Houck, W. Ted Brown, Stephanie L. Sherman, W. Ted Brown, Andrew G. Hadd, Gary J. Latham, W. Ted Brown and Xiaohua Ding and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Cell Biology and Biochemical and Biophysical Research Communications.

In The Last Decade

Sarah L. Nolin

44 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sarah L. Nolin United States 21 1.4k 927 833 135 83 44 1.6k
Jack Tarleton United States 19 1.5k 1.1× 749 0.8× 1.0k 1.2× 188 1.4× 162 2.0× 50 1.9k
Anne Glicksman United States 14 1.0k 0.7× 693 0.7× 519 0.6× 93 0.7× 55 0.7× 18 1.1k
F. Rousseau France 10 1.3k 0.9× 579 0.6× 1.0k 1.2× 170 1.3× 42 0.5× 21 1.7k
Ben A. Oostra Netherlands 11 1.4k 1.0× 758 0.8× 1.1k 1.3× 213 1.6× 25 0.3× 12 1.6k
Seungtai Yoon United States 10 1.0k 0.7× 433 0.5× 821 1.0× 67 0.5× 41 0.5× 16 1.5k
George E. Houck United States 14 752 0.5× 456 0.5× 447 0.5× 62 0.5× 66 0.8× 26 909
Jyotsna Sudi United States 13 1.0k 0.7× 451 0.5× 705 0.8× 148 1.1× 189 2.3× 14 1.5k
Amy Cronister United States 16 1.3k 0.9× 802 0.9× 580 0.7× 65 0.5× 269 3.2× 21 1.5k
John B. Vincent Canada 11 878 0.6× 539 0.6× 656 0.8× 113 0.8× 24 0.3× 19 1.1k
Martine Borghgraef Belgium 18 780 0.5× 408 0.4× 381 0.5× 50 0.4× 76 0.9× 54 925

Countries citing papers authored by Sarah L. Nolin

Since Specialization
Citations

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

Fields of papers citing papers by Sarah L. Nolin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sarah L. Nolin. 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 Sarah L. Nolin. The network helps show where Sarah L. Nolin may publish in the future.

Co-authorship network of co-authors of Sarah L. Nolin

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah L. Nolin. A scholar is included among the top collaborators of Sarah L. Nolin 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 Sarah L. Nolin. Sarah L. Nolin 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.
Yrigollen, Carolyn M., Flora Tassone, Olatz Villate, et al.. (2024). FMR1 allelic complexity in premutation carriers provides no evidence for a correlation with age at amenorrhea. Reproductive Biology and Endocrinology. 22(1). 71–71. 1 indexed citations
2.
Nolin, Sarah L., et al.. (2021). Deficits in Prenatal Serine Biosynthesis Underlie the Mitochondrial Dysfunction Associated with the Autism-Linked FMR1 Gene. International Journal of Molecular Sciences. 22(11). 5886–5886. 9 indexed citations
3.
Allen, Emily G., Krista Charen, Heather S. Hipp, et al.. (2021). Refining the risk for fragile X–associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size. Genetics in Medicine. 23(9). 1648–1655. 31 indexed citations
4.
Hayward, Bruce E., Xiaohua Ding, Sarah L. Nolin, et al.. (2019). Fragile X syndrome in a male with methylated premutation alleles and no detectable methylated full mutation alleles. American Journal of Medical Genetics Part A. 179(10). 2132–2137. 5 indexed citations
5.
Nolin, Sarah L., Anne Glicksman, Emily G. Allen, et al.. (2019). Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles. American Journal of Medical Genetics Part A. 179(7). 1148–1156. 47 indexed citations
6.
Cohen, Yoram, Michal Berkenstadt, Elon Pras, et al.. (2018). Absence of AGG Interruptions Is a Risk Factor for Full Mutation Expansion Among Israeli FMR1 Premutation Carriers. Frontiers in Genetics. 9. 606–606. 13 indexed citations
7.
Allen, Emily G., Anne Glicksman, Krista Charen, et al.. (2018). FXPOI: Pattern of AGG Interruptions Does not Show an Association With Age at Amenorrhea Among Women With a Premutation. Frontiers in Genetics. 9. 292–292. 7 indexed citations
8.
Nolin, Sarah L., Sachin Sah, Anne Glicksman, et al.. (2013). Fragile X AGG analysis provides new risk predictions for 45–69 repeat alleles. American Journal of Medical Genetics Part A. 161(4). 771–778. 99 indexed citations
9.
LaFauci, Giuseppe, Tatyana Adayev, Richard J. Kascsak, et al.. (2013). Fragile X Screening by Quantification of FMRP in Dried Blood Spots by a Luminex Immunoassay. Journal of Molecular Diagnostics. 15(4). 508–517. 43 indexed citations
10.
Dobkin, Carl, et al.. (2009). Fragile X prenatal analyses show full mutation females at high risk for mosaic Turner syndrome: Fragile X leads to chromosome loss. American Journal of Medical Genetics Part A. 149A(10). 2152–2157. 25 indexed citations
11.
Nolin, Sarah L., Xiaohua Ding, George E. Houck, W. Ted Brown, & Carl Dobkin. (2007). Fragile X full mutation alleles composed of few alleles: Implications for CGG repeat expansion. American Journal of Medical Genetics Part A. 146A(1). 60–65. 18 indexed citations
12.
Dolzhanskaya, Natalia, et al.. (2003). The Fragile X Mental Retardation Protein FMRP Binds Elongation Factor 1A mRNA and Negatively Regulates Its Translation in Vivo. Journal of Biological Chemistry. 278(18). 15669–15678. 80 indexed citations
13.
Brown, W. Ted & Sarah L. Nolin. (2000). Invited Commentary: Apparent FMR1 Allele Instability in Non-Fragile X Males. Genetic Testing. 4(3). 241–242. 1 indexed citations
14.
Nolin, Sarah L., et al.. (1999). FMR1 CGG-Repeat Instability in Single Sperm and Lymphocytes of Fragile-X Premutation Males. The American Journal of Human Genetics. 65(3). 680–688. 30 indexed citations
15.
Jenkins, Edmund C., G. Y. Wen, Kwang Soo Kim, et al.. (1999). Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies. American Journal of Medical Genetics. 83(4). 342–346. 7 indexed citations
16.
Dobkin, Carl, et al.. (1999). Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection. American Journal of Medical Genetics. 83(4). 338–341. 6 indexed citations
17.
Cohen, Ira L., Sarah L. Nolin, Vicki Sudhalter, et al.. (1996). Mosaicism for theFMR1 gene influences adaptive skills development in fragile X-affected males. American Journal of Medical Genetics. 64(2). 365–369. 40 indexed citations
18.
Brown, W. Ted, Sarah L. Nolin, George E. Houck, et al.. (1996). Prenatal diagnosis and carrier screening for fragile X by PCR. American Journal of Medical Genetics. 64(1). 191–195. 54 indexed citations
19.
Nolin, Sarah L. & Carl Dobkin. (1991). Cloning the ends of size selected Sfi I fragments. American Journal of Medical Genetics. 38(2-3). 384–390. 1 indexed citations
20.
Nolin, Sarah L., Edmund C. Jenkins, Michael S. Krawczun, et al.. (1991). Fragile X screening program in New York State. American Journal of Medical Genetics. 38(2-3). 251–255. 29 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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