Lynn Pais

2.2k citations

19 papers · 168 indexed · h-index 7

Co-authors: Susan M. White Tiong Yang Tan Zornitza Stark Cas Simons John Christodoulou Chloe Stutterd Katherine B. Howell Rachel Straussberg
Topics: Cancer Genomics and Diagnostics (3 papers)Genomics and Rare Diseases (2 papers)Mitochondrial Function and Pathology (2 papers)
Cited by: Genetics Immunology and Allergy
Journals: Development The American Journal of Human Genetics Human Molecular Genetics
Partner nations: United States Australia Türkiye

In The Last Decade

Lynn Pais

16 papers receiving 165 citations

Peers

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

#	Work	Indexed citations
1	Neurogenic arthrogryposis, hypotonia, dysmorphic features plus malformation of cortical development further expands the ARL6IP1 loss-of-function phenotype 2025 ·Neuromuscular Disorders ·Göknur Haliloğlu,(unknown),(unknown),Ikeoluwa Osei‐Owusu,Lynn Pais,(unknown),Beril Talim,Rahşan Göçmen,Serdar Ceylaner,Carsten G. Bönnemann	1
2	Novel Phenotypes and Genotype–Phenotype Correlations in a Large Clinical Cohort of Patients With Kleefstra Syndrome 2025 ·Clinical Genetics ·(unknown),(unknown),(unknown),Alisa Mo,Maryanne Quinn,Sonia Ballal,Tamar Katz,A. Eliot Shearer,Max A. Horlbeck,Lynn Pais,Kira A. Dies,Anne O’Donnell‐Luria,Joe Kossowsky,Jonathan O. Lipton,Tjitske Kleefstra,Siddharth Srivastava	1
3	Male proband with intractable seizures and a de novo start-codon-disrupting variant in GLUL 2025 ·Human Genetics and Genomics Advances ·(unknown),Sarah L. Stenton,(unknown),(unknown),Grace E. VanNoy,Lynn Pais,John Gaitanis,Melanie O’Leary,Heidi L. Rehm,Anne O’Donnell‐Luria	0
4	Protein‐extending ACTN2 frameshift variants cause variable myopathy phenotypes by protein aggregation 2024 ·Annals of Clinical and Translational Neurology ·(unknown),Kevin J. Felice,Per Harald Jonson,J. Sarparanta,(unknown),Inès Harzallah,Renaud Touraine,Lynn Pais,Christina Austin‐Tse,Vijay Ganesh,(unknown),Heidi L. Rehm,Michael K. Hehir,S. H. Subramony,Qian Wu,Bjarne Udd,Marco Savarese	1
5	Distinct whole-body muscle MRI imaging patterns in PAX7-congenital myopathy: A case report 2024 ·Journal of Neuromuscular Diseases ·Göknur Haliloğlu,(unknown),(unknown),(unknown),Ying Hu,Lynn Pais,Robert Carlier,Helge Amthor,Üstün Aydıngöz,Carsten G. Bönnemann	0
6	Erythromelalgia caused by the missense mutation p.Arg220Pro in an alternatively spliced exon of SCN9A (NaV1.7) 2023 ·Human Molecular Genetics ·Jennifer R. Deuis,Smitha Kumble,Angelo Keramidas,Lotten Ragnarsson,Cas Simons,Lynn Pais,Susan M. White,Irina Vetter	1
7	Maternal Malignancy After Atypical Findings on Single-Nucleotide Polymorphism–Based Prenatal Cell-Free DNA Screening 2023 ·Obstetrics and Gynecology ·(unknown),(unknown),(unknown),Vivienne Souter,Lynn Pais,(unknown),Wenbo Xu,Jeffrey N. Weitzel,Neeta L. Vora	8
8	P285 Bi-allelic variants in HMGCR cause limb girdle muscular dystrophy and further implicate the mevalonate pathway in muscle disease 2023 ·Neuromuscular Disorders ·A. Reghan Foley,Sandra Donkervoort,Diana Bharucha‐Goebel,Dimah Saade,(unknown),(unknown),Ying Hu,(unknown),(unknown),Elicia Estrella,(unknown),Katherine R. Chao,Lynn Pais,Louis M. Kunkel,Peter B. Kang,Carsten G. Bönnemann	1
9	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 2023 ·American Journal of Medical Genetics Part A ·(unknown),John Christodoulou,David R. Thorburn,Jeremy L. Freeman,Andrew J. Kornberg,Simone Mandelstam,Alison G. Compton,Beryl B. Cummings,Lynn Pais,Joy Yaplito‐Lee,Susan M. White	3
10	Maternal Malignancy After Atypical Findings on Single-Nucleotide Polymorphism-Based Prenatal Cell-Free DNA Screening 2023 ·Obstetrical & Gynecological Survey ·(unknown),(unknown),(unknown),Vivienne Souter,Lynn Pais,(unknown),Wenbo Xu,Jeffrey N. Weitzel,Neeta L. Vora	2
11	Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability 2021 ·European Journal of Human Genetics ·Natja Haag,Ene‐Choo Tan,Matthias Begemann,(unknown),Florian Kraft,(unknown),Angeline Lai,Maggie Brett,Ganeshwaran H. Mochida,Stephanie DiTroia,Lynn Pais,Jennifer E. Neil,Muna Al‐Saffar,Lailá Bastaki,Christopher A. Walsh,Ingo Kurth,Cordula Knopp	6
12	Genetic Study in a Cohort of Children With ROHHAD Syndrome 2021 ·Journal of the Endocrine Society ·(unknown),(unknown),Lynn Pais,(unknown),(unknown),(unknown),Casie A. Genetti,(unknown),John M. Schreiber,(unknown),Emre E. Turer,Amina Kurtović-Kozarić,Klaus Schmitz‐Abe,(unknown),Jonathan Picker,Joel N. Hirschhorn,Pankaj B. Agrawal,Vidhu Thaker	3
13	Pathogenic variants in nucleoporin TPR (translocated promoter region, nuclear basket protein) cause severe intellectual disability in humans 2021 ·Human Molecular Genetics ·Nicole J. Van Bergen,Katrina M. Bell,(unknown),(unknown),(unknown),(unknown),Lyndon Gallacher,Kate Pope,Paul J. Lockhart,Andrew J. Kornberg,Lynn Pais,Marzena Walkiewicz,Cas Simons,(unknown),Vihandha O. Wickramasinghe,Susan M. White,John Christodoulou	4
14	Multiomic analysis elucidates Complex I deficiency caused by a deep intronic variant in NDUFB10 2020 ·Human Mutation ·Guy Helman,Alison G. Compton,Daniella H. Hock,Marzena Walkiewicz,Gemma R. Brett,Lynn Pais,Tiong Yang Tan,Ricardo De Paoli‐Iseppi,Michael B. Clark,John Christodoulou,Susan M. White,David R. Thorburn,David A. Stroud,Zornitza Stark,Cas Simons	18
15	Bi-allelic ADARB1 Variants Associated with Microcephaly, Intellectual Disability, and Seizures 2020 ·The American Journal of Human Genetics ·Tiong Yang Tan,Jiří Sedmík,Mark P. Fitzgerald,Rivka Sukenik‐Halevy,Liam P. Keegan,Ingo Helbig,Lina Basel‐Salmon,Lior Cohen,Rachel Straussberg,Wendy K. Chung,(unknown),Reza Maroofian,Henry Houlden,Jane Juusola,Simon Sadedin,Lynn Pais,Katherine B. Howell,Susan M. White,John Christodoulou,Mary A. O’Connell	34
16	Evaluating systematic reanalysis of clinical genomic data in rare disease from single center experience and literature review 2020 ·Molecular Genetics & Genomic Medicine ·Natalie B. Tan,Rachel Stapleton,Zornitza Stark,Martin B. Delatycki,Alison Yeung,Matthew F. Hunter,David J. Amor,Natasha J. Brown,Chloe Stutterd,George McGillivray,Patrick Yap,Matthew Regan,Belinda Chong,Miriam Fanjul‐Fernández,Justine E. Marum,Dean Phelan,Lynn Pais,Susan M. White,Sebastian Lunke,Tiong Yang Tan	44
17	A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder 2020 ·Development ·Lynelle K. Jones,Rachel Lam,Karen K. McKee,Maya Aleksandrova,(unknown),Stephen I. Alexander,Amali Mallawaarachchi,Denny L. Cottle,Kieran M. Short,Lynn Pais,(unknown),Andrew J. Mallett,Cas Simons,Hugh J. McCarthy,Peter D. Yurchenco,Ian Smyth	22
18	Mutations analysis of C1 inhibitor coding sequence gene among Portuguese patients with hereditary angioedema 2012 ·Molecular Immunology ·(unknown),José João Mendes,(unknown),(unknown),(unknown),(unknown),Paula Pinto,Manuel Branco Ferreira,Celso Pereira,(unknown),Lynn Pais	17
19	A Story Told: Organizing School Social Workers to Serve in the Public Schools of San Antonio, Texas 2002 ·Children & Schools ·(unknown),Lynn Pais,(unknown)	2

About Lynn Pais

Lynn Pais is a scholar working on Genetics, Molecular Biology and Cancer Research, having authored 19 papers that have together received 168 indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (3 papers), Genomics and Rare Diseases (2 papers) and Mitochondrial Function and Pathology (2 papers). The work is most often cited by research in Genetics (24 citations), Genetics (52 citations) and Immunology and Allergy (11 citations). Lynn Pais has collaborated with scholars based in United States, Australia and Türkiye. Frequent 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. Their work appears in journals such as Development, The American Journal of Human Genetics and Human Molecular Genetics.

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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