Lynn Pais

2.2k total citations
19 papers, 168 citations indexed

About

Lynn Pais is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Lynn Pais has authored 19 papers receiving a total of 168 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Genetics. Recurrent topics in Lynn Pais's work include Cancer Genomics and Diagnostics (3 papers), Genomics and Rare Diseases (2 papers) and Mitochondrial Function and Pathology (2 papers). Lynn Pais is often cited by papers focused on Cancer Genomics and Diagnostics (3 papers), Genomics and Rare Diseases (2 papers) and Mitochondrial Function and Pathology (2 papers). Lynn Pais collaborates with scholars based in United States, Australia and Türkiye. Lynn Pais's co-authors include Susan M. White, Tiong Yang Tan, Zornitza Stark, Cas Simons, John Christodoulou, Chloe Stutterd, Katherine B. Howell, Rachel Straussberg, Wendy K. Chung and Lior Cohen and has published in prestigious journals such as Development, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Lynn Pais

16 papers receiving 165 citations

Peers

Lynn Pais

GENET

PPCH

Samantha Penney United States

Yaser Heshmati Sweden

Tova Hershkovitz Israel

Htoo A. Wai United Kingdom

Andrei M. Vacaru United States

Mohammad Al-Owain Saudi Arabia

Bita Bozorgmehr Iran

Monika Weisz Hubshman Israel

Salima El Chehadeh-Djebbar France

Adam C. Gunning United Kingdom

Samantha Penney United States

Lynn Pais

68 ×0.7

76 ×1.5

GENET

27 ×1.0

18 ×0.8

GENET

14 ×0.7

PPCH

Citations per year, relative to Lynn Pais Lynn Pais (= 1×) peers Samantha Penney

Countries citing papers authored by Lynn Pais

Since Specialization

Citations

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

Fields of papers citing papers by Lynn Pais

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lynn Pais

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

All Works

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19 of 19 papers shown

Haliloğlu, Göknur, Ikeoluwa Osei‐Owusu, Lynn Pais, et al.. (2025). Neurogenic arthrogryposis, hypotonia, dysmorphic features plus malformation of cortical development further expands the ARL6IP1 loss-of-function phenotype. Neuromuscular Disorders. 48. 105312–105312. 1 indexed citations

Mo, Alisa, Maryanne Quinn, Sonia Ballal, et al.. (2025). Novel Phenotypes and Genotype–Phenotype Correlations in a Large Clinical Cohort of Patients With Kleefstra Syndrome. Clinical Genetics. 107(6). 636–645. 1 indexed citations

Stenton, Sarah L., Grace E. VanNoy, Lynn Pais, et al.. (2025). Male proband with intractable seizures and a de novo start-codon-disrupting variant in GLUL. Human Genetics and Genomics Advances. 6(2). 100419–100419.

Felice, Kevin J., Per Harald Jonson, J. Sarparanta, et al.. (2024). Protein‐extending ACTN2 frameshift variants cause variable myopathy phenotypes by protein aggregation. Annals of Clinical and Translational Neurology. 11(9). 2392–2405. 1 indexed citations

Haliloğlu, Göknur, Ying Hu, Lynn Pais, et al.. (2024). Distinct whole-body muscle MRI imaging patterns in PAX7-congenital myopathy: A case report. Journal of Neuromuscular Diseases. 11(6). 1276–1282.

Deuis, Jennifer R., Smitha Kumble, Angelo Keramidas, et al.. (2023). Erythromelalgia caused by the missense mutation p.Arg220Pro in an alternatively spliced exon of SCN9A (NaV1.7). Human Molecular Genetics. 33(2). 103–109. 1 indexed citations

Souter, Vivienne, et al.. (2023). Maternal Malignancy After Atypical Findings on Single-Nucleotide Polymorphism–Based Prenatal Cell-Free DNA Screening. Obstetrics and Gynecology. 141(4). 791–800. 8 indexed citations

Foley, A. Reghan, Sandra Donkervoort, Diana Bharucha‐Goebel, et al.. (2023). P285 Bi-allelic variants in HMGCR cause limb girdle muscular dystrophy and further implicate the mevalonate pathway in muscle disease. Neuromuscular Disorders. 33. S114–S114. 1 indexed citations

Christodoulou, John, David R. Thorburn, Jeremy L. Freeman, et al.. (2023). A cryptic pathogenic NDUFV1 variant identified by RNA‐seq in a patient with normal complex I activity in muscle and transient magnetic resonance imaging changes. American Journal of Medical Genetics Part A. 191(6). 1599–1606. 3 indexed citations

10.

Souter, Vivienne, et al.. (2023). Maternal Malignancy After Atypical Findings on Single-Nucleotide Polymorphism-Based Prenatal Cell-Free DNA Screening. Obstetrical & Gynecological Survey. 78(10). 570–571. 2 indexed citations

11.

Haag, Natja, Ene‐Choo Tan, Matthias Begemann, et al.. (2021). Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability. European Journal of Human Genetics. 29(11). 1663–1668. 6 indexed citations

12.

Pais, Lynn, Casie A. Genetti, John M. Schreiber, et al.. (2021). Genetic Study in a Cohort of Children With ROHHAD Syndrome. Journal of the Endocrine Society. 5(Supplement_1). A503–A504. 3 indexed citations

13.

Bergen, Nicole J. Van, Katrina M. Bell, Lyndon Gallacher, et al.. (2021). Pathogenic variants in nucleoporin TPR (translocated promoter region, nuclear basket protein) cause severe intellectual disability in humans. Human Molecular Genetics. 31(3). 362–375. 4 indexed citations

14.

Helman, Guy, Alison G. Compton, Daniella H. Hock, et al.. (2020). Multiomic analysis elucidates Complex I deficiency caused by a deep intronic variant in NDUFB10. Human Mutation. 42(1). 19–24. 18 indexed citations

15.

Tan, Tiong Yang, Jiří Sedmík, Mark P. Fitzgerald, et al.. (2020). Bi-allelic ADARB1 Variants Associated with Microcephaly, Intellectual Disability, and Seizures. The American Journal of Human Genetics. 106(4). 467–483. 34 indexed citations

16.

Tan, Natalie B., Rachel Stapleton, Zornitza Stark, et al.. (2020). Evaluating systematic reanalysis of clinical genomic data in rare disease from single center experience and literature review. Molecular Genetics & Genomic Medicine. 8(11). e1508–e1508. 44 indexed citations

17.

Jones, Lynelle K., Rachel Lam, Karen K. McKee, et al.. (2020). A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder. Development. 147(21). 22 indexed citations

18.

Mendes, José João, et al.. (2012). Mutations analysis of C1 inhibitor coding sequence gene among Portuguese patients with hereditary angioedema. Molecular Immunology. 53(4). 431–434. 17 indexed citations

19.

Pais, Lynn, et al.. (2002). A Story Told: Organizing School Social Workers to Serve in the Public Schools of San Antonio, Texas. Children & Schools. 24(4). 247–259. 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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