Louisa Kalsner

688 total citations
14 papers, 247 citations indexed

About

Louisa Kalsner is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Louisa Kalsner has authored 14 papers receiving a total of 247 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Cognitive Neuroscience. Recurrent topics in Louisa Kalsner's work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Louisa Kalsner is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Louisa Kalsner collaborates with scholars based in United States, Germany and Switzerland. Louisa Kalsner's co-authors include Stormy J. Chamberlain, Justin Cotney, Antonio R. Pérez‐Atayde, Jonathan E. Teitelbaum, Michael J. Rivkin, Christine M. Stanley, Douglas C. Anthony, Victor L. Fox, Ricardo Fadić and Thyde Dumont‐Mathieu and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and The American Journal of Surgical Pathology.

In The Last Decade

Louisa Kalsner

14 papers receiving 245 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Louisa Kalsner United States	6	150	126	66	30	27	14	247
Daniel Amsallem France	10	222 1.5×	173 1.4×	81 1.2×	29 1.0×	10 0.4×	21	335
Carmen Esmer Mexico	5	157 1.0×	116 0.9×	46 0.7×	33 1.1×	10 0.4×	16	225
Dima El‐Khechen United States	8	208 1.4×	125 1.0×	49 0.7×	26 0.9×	15 0.6×	10	294
Radha Rama Devi Akella India	8	97 0.6×	84 0.7×	86 1.3×	32 1.1×	18 0.7×	14	252
Anne Chun‐Hui Tsai United States	10	117 0.8×	126 1.0×	27 0.4×	47 1.6×	37 1.4×	22	295
Erika Carter United States	10	268 1.8×	118 0.9×	21 0.3×	82 2.7×	26 1.0×	15	338
Naghmeh Dorrani United States	12	367 2.4×	314 2.5×	132 2.0×	37 1.2×	13 0.5×	20	518
Dimitar N. Azmanov Australia	12	122 0.8×	191 1.5×	11 0.2×	53 1.8×	11 0.4×	23	336
Emma McCann United Kingdom	6	177 1.2×	153 1.2×	14 0.2×	80 2.7×	10 0.4×	10	315
Eve Õiglane‐Shlik Estonia	10	185 1.2×	177 1.4×	17 0.3×	76 2.5×	10 0.4×	17	320

Countries citing papers authored by Louisa Kalsner

Since Specialization

Citations

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

Fields of papers citing papers by Louisa Kalsner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Louisa Kalsner

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

All Works

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14 of 14 papers shown

Kalsner, Louisa, Purva Vats, Peter A. Audano, et al.. (2025). Phenotypic Expansion of Knobloch Syndrome Type 2 in an Individual With a De Novo PAK2 Variant. American Journal of Medical Genetics Part A. 197(6). e64006–e64006. 1 indexed citations

Schnur, Rhonda E., Louisa Kalsner, Dana Grebeňová, et al.. (2024). New kinase‐deficient PAK2 variants associated with Knobloch syndrome type 2. Clinical Genetics. 106(4). 518–524. 4 indexed citations

Kennedy, Craig H., et al.. (2024). Health Condition Co-Morbidities in Children with Autism and Their Association with Challenging Behavior. Advances in Neurodevelopmental Disorders. 9(1). 64–70. 1 indexed citations

Graf, W., Bruce H. Cohen, Louisa Kalsner, et al.. (2023). Fetal anomaly diagnosis and termination of pregnancy. Developmental Medicine & Child Neurology. 65(7). 900–907. 10 indexed citations

Lipska‐Ziętkiewicz, Beata S., Vincent Michaud, James Lespinasse, et al.. (2022). Phenotypic characterization of seven individuals with Marbach–Schaaf neurodevelopmental syndrome. American Journal of Medical Genetics Part A. 188(9). 2627–2636. 3 indexed citations

Koprulu, Mine, Muhammad Shuaib, Nara Sobreira, et al.. (2020). Biallelic ZNF407 mutations in a neurodevelopmental disorder with ID, short stature and variable microcephaly, hypotonia, ocular anomalies and facial dysmorphism. Journal of Human Genetics. 65(12). 1115–1123. 3 indexed citations

Slavotinek, Anne, Johanna M. van Hagen, Louisa Kalsner, et al.. (2020). Jumonji domain containing 1C (JMJD1C) sequence variants in seven patients with autism spectrum disorder, intellectual disability and seizures. European Journal of Medical Genetics. 63(4). 103850–103850. 2 indexed citations

Hiatt, Susan M., Michelle L. Thompson, Jeremy W. Prokop, et al.. (2019). Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder. The American Journal of Human Genetics. 104(4). 701–708. 15 indexed citations

Asad, Syed Daniyal, et al.. (2019). FOXG1 syndrome: A rare disorder often misdiagnosed as cerebral palsy (P1.6-045). Neurology. 92(15_supplement). 1 indexed citations

10.

Kalsner, Louisa, et al.. (2018). Yield of Genetic Testing Including Targeted Gene Panel in a Clinical Population of Children with Autism Spectrum Disorder (P1.303). Neurology. 90(15_supplement). 2 indexed citations

11.

Zárate, Yuri A., Louisa Kalsner, Alice Basinger, et al.. (2017). Genotype and phenotype in 12 additional individuals with SATB2‐associated syndrome. Clinical Genetics. 92(4). 423–429. 28 indexed citations

12.

Kalsner, Louisa, et al.. (2017). Genetic testing including targeted gene panel in a diverse clinical population of children with autism spectrum disorder: Findings and implications. Molecular Genetics & Genomic Medicine. 6(2). 171–185. 32 indexed citations

13.

Kalsner, Louisa & Stormy J. Chamberlain. (2015). Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes. Pediatric Clinics of North America. 62(3). 587–606. 98 indexed citations

14.

Pérez‐Atayde, Antonio R., Victor L. Fox, Jonathan E. Teitelbaum, et al.. (1998). Mitochondrial Neurogastrointestinal Encephalomyopathy. The American Journal of Surgical Pathology. 22(9). 1141–1147. 47 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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