Laura K. Conlin

6.9k total citations
73 papers, 2.5k citations indexed

About

Laura K. Conlin is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Laura K. Conlin has authored 73 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Genetics, 33 papers in Molecular Biology and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Laura K. Conlin's work include Genomic variations and chromosomal abnormalities (34 papers), Genomics and Rare Diseases (15 papers) and Prenatal Screening and Diagnostics (14 papers). Laura K. Conlin is often cited by papers focused on Genomic variations and chromosomal abnormalities (34 papers), Genomics and Rare Diseases (15 papers) and Prenatal Screening and Diagnostics (14 papers). Laura K. Conlin collaborates with scholars based in United States, United Kingdom and Japan. Laura K. Conlin's co-authors include Nancy B. Spinner, Matthew A. Deardorff, Kuang‐Yu Jen, Teresa M. Weber, Richard S. Spielman, Vivian G. Cheung, Elaine H. Zackai, Michael P. Morley, Ian D. Krantz and Håkon Håkonarson and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Laura K. Conlin

72 papers receiving 2.4k citations

Peers

Laura K. Conlin

GENET

PPCH

Swaroop Aradhya United States

Nicole de Leeuw Netherlands

Ana Cristina Victorino Krepischi Brazil

Matthew A. Deardorff United States

Claudia Ruivenkamp Netherlands

Bassem A. Bejjani United States

Jürgen Horst Germany

Evica Rajcan‐Separovic Canada

Sarina G. Kant Netherlands

Alan Shanske United States

Swaroop Aradhya United States

Laura K. Conlin

1.9k ×1.2

GENET

1.2k ×1.0

590 ×1.1

PPCH

145 ×0.6

278 ×1.7

Citations per year, relative to Laura K. Conlin Laura K. Conlin (= 1×) peers Swaroop Aradhya

Countries citing papers authored by Laura K. Conlin

Since Specialization

Citations

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

Fields of papers citing papers by Laura K. Conlin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laura K. Conlin. 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 Laura K. Conlin. The network helps show where Laura K. Conlin may publish in the future.

Co-authorship network of co-authors of Laura K. Conlin

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

All Works

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20 of 20 papers shown

Iwata‐Otsubo, Aiko, Jorune Balciuniene, Cara Skraban, et al.. (2025). 16q24.3 Microdeletions Disrupting Upstream Non-Coding Region of ANKRD11 Cause KBG Syndrome. Genes. 16(2). 136–136. 1 indexed citations

Wild, K. Taylor, Laura K. Conlin, Michael A. Manfredi, et al.. (2024). Genomic Contributors to Esophageal Atresia and Tracheoesophageal Fistula: A 12 Year Retrospective Review. The Journal of Pediatrics. 271. 114060–114060. 1 indexed citations

Luo, Minjie, Derek Wong, Kristin Zelley, et al.. (2024). Identification of TP53 germline variants in pediatric patients undergoing tumor testing: strategy and prevalence. JNCI Journal of the National Cancer Institute. 116(8). 1356–1365. 2 indexed citations

Lebo, Matthew S., Marcie Steeves, Laura K. Conlin, et al.. (2023). O31: Risk allele evidence curation, classification, and reporting: Recommendations from the ClinGen Low Penetrance/Risk Allele Working Group*. SHILAP Revista de lepidopterología. 1(1). 100457–100457. 3 indexed citations

Wu, Chao, Batsal Devkota, Perry Evans, et al.. (2019). Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approach. European Journal of Human Genetics. 27(4). 612–620. 10 indexed citations

Sheppard, Sarah E., Emilie Lalonde, N. Scott Adzick, et al.. (2019). Androgenetic chimerism as an etiology for Beckwith–Wiedemann syndrome: diagnosis and management. Genetics in Medicine. 21(11). 2644–2649. 12 indexed citations

Waggoner, Darrel, Karen E. Wain, Adrian M. Dubuc, et al.. (2018). Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 20(10). 1105–1113. 46 indexed citations

Guan, Qiaoning, Jorune Balciuniene, Kajia Cao, et al.. (2018). AUDIOME: a tiered exome sequencing–based comprehensive gene panel for the diagnosis of heterogeneous nonsyndromic sensorineural hearing loss. Genetics in Medicine. 20(12). 1600–1608. 27 indexed citations

Romasko, Edward J., Batsal Devkota, Sawona Biswas, et al.. (2017). Utility and limitations of exome sequencing in the molecular diagnosis of pediatric inherited platelet disorders. American Journal of Hematology. 93(1). 8–16. 22 indexed citations

10.

Mulchandani, Surabhi, Elizabeth Bhoj, Minjie Luo, et al.. (2015). Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure. Genetics in Medicine. 18(4). 309–315. 73 indexed citations

11.

Spinner, Nancy B. & Laura K. Conlin. (2014). Mosaicism and clinical genetics. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 166(4). 397–405. 47 indexed citations

12.

Li, Qiaoli, Jill L. Brodsky, Laura K. Conlin, et al.. (2013). Mutations in the ABCC6 Gene as a Cause of Generalized Arterial Calcification of Infancy: Genotypic Overlap with Pseudoxanthoma Elasticum. Journal of Investigative Dermatology. 134(3). 658–665. 59 indexed citations

13.

Kalish, Jennifer M., Laura K. Conlin, Sogol Mostoufi‐Moab, et al.. (2013). Bilateral Pheochromocytomas, Hemihyperplasia, and Subtle Somatic Mosaicism: The Importance of Detecting Low‐Level Uniparental Disomy. American Journal of Medical Genetics Part A. 161(5). 993–1001. 15 indexed citations

14.

Akizu, Naiara, Tawfeg Ben‐Omran, Lailá Bastaki, et al.. (2013). Whole-Exome Sequencing Identifies Mutated C12orf57 in Recessive Corpus Callosum Hypoplasia. The American Journal of Human Genetics. 92(3). 392–400. 19 indexed citations

15.

Daber, Robert, Laura K. Conlin, Laura D. Leonard, et al.. (2012). Ring chromosome 20. European Journal of Medical Genetics. 55(5). 381–387. 48 indexed citations

16.

Hosain, Syed, Laura K. Conlin, & Nancy B. Spinner. (2012). Ring chromosome 20 epilepsy syndrome: An overview. 1(1). 5–10. 2 indexed citations

17.

Crowley, Moira, Laura K. Conlin, Elaine H. Zackai, et al.. (2010). Further evidence for the possible role of MEIS2 in the development of cleft palate and cardiac septum. American Journal of Medical Genetics Part A. 152A(5). 1326–1327. 41 indexed citations

18.

Sampson, Matthew G., Curtis R. Coughlin, Paige Kaplan, et al.. (2010). Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease. American Journal of Medical Genetics Part A. 152A(10). 2618–2622. 37 indexed citations

19.

Kamath, Binita M., Brian Thiel, Xiaowu Gai, et al.. (2008). SNP array mapping of chromosome 20p deletions: Genotypes, phenotypes, and copy number variation. Human Mutation. 30(3). 371–378. 46 indexed citations

20.

Swoyer, J, Patrick W. Irvine, L Sackett-Lundeen, et al.. (1989). Circadian Hematologic Time Structure in the Elderly. Chronobiology International. 6(2). 131–137. 18 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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