David Bick

41.8k total citations · 2 hit papers
83 papers, 22.0k citations indexed

About

David Bick is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, David Bick has authored 83 papers receiving a total of 22.0k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Genetics, 25 papers in Molecular Biology and 16 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in David Bick's work include Genomics and Rare Diseases (30 papers), Genomic variations and chromosomal abnormalities (21 papers) and Prenatal Screening and Diagnostics (14 papers). David Bick is often cited by papers focused on Genomics and Rare Diseases (30 papers), Genomic variations and chromosomal abnormalities (21 papers) and Prenatal Screening and Diagnostics (14 papers). David Bick collaborates with scholars based in United States, United Kingdom and Türkiye. David Bick's co-authors include Heidi L. Rehm, Soma Das, Elaine Lyon, Madhuri Hegde, Karl V. Voelkerding, Sherri J. Bale, Wayne W. Grody, Julie M. Gastier‐Foster, Elaine Spector and Nazneen Aziz and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

David Bick

81 papers receiving 21.7k citations

Hit Papers

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What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

2015 18.9k citations Sue Richards, Nazneen Aziz et al. Genetics in Medicine profile →
Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome

1989 451 citations David Bick et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
David Bick	10.4k	10.3k	2.1k	1.8k	1.7k	83	22.0k
Elaine Lyon	10.9k 1.0×	10.3k 1.0×	2.2k 1.1×	2.3k 1.3×	1.8k 1.0×	102	23.2k
Karl V. Voelkerding	11.2k 1.1×	9.8k 0.9×	2.2k 1.0×	2.6k 1.4×	1.7k 1.0×	86	23.1k
Elaine Spector	10.1k 1.0×	9.0k 0.9×	2.1k 1.0×	1.7k 0.9×	1.7k 1.0×	71	20.6k
Nazneen Aziz	9.4k 0.9×	8.8k 0.9×	2.1k 1.0×	1.9k 1.0×	1.6k 0.9×	9	19.7k
Madhuri Hegde	11.5k 1.1×	10.7k 1.0×	2.4k 1.1×	2.6k 1.4×	1.8k 1.0×	138	23.8k
Julie M. Gastier‐Foster	10.4k 1.0×	9.0k 0.9×	2.2k 1.0×	2.2k 1.2×	1.8k 1.0×	122	22.8k
Sue Richards	9.6k 0.9×	8.7k 0.9×	2.1k 1.0×	1.8k 1.0×	1.6k 0.9×	85	22.4k
Sherri J. Bale	14.7k 1.4×	12.9k 1.3×	2.4k 1.1×	2.9k 1.6×	1.9k 1.1×	142	29.9k
Wayne W. Grody	11.9k 1.1×	12.1k 1.2×	2.5k 1.2×	3.1k 1.7×	2.1k 1.2×	168	28.7k
Egbert Bakker	7.2k 0.7×	4.1k 0.4×	1.4k 0.7×	814 0.4×	638 0.4×	246	12.3k

Countries citing papers authored by David Bick

Since Specialization

Citations

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

Fields of papers citing papers by David Bick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Bick

This figure shows the co-authorship network connecting the top 25 collaborators of David Bick. A scholar is included among the top collaborators of David Bick 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 David Bick. David Bick 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

Lao, Qizong, et al.. (2025). Clinical and Biochemical Phenotype Across the Genotypic Spectrum of 21-hydroxylase Deficiency in 457 Individuals. The Journal of Clinical Endocrinology & Metabolism. 111(4). 1098–1113.

Wigby, Kristen, Deanna Brockman, Gregory Costain, et al.. (2024). Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders. npj Genomic Medicine. 9(1). 15–15. 8 indexed citations

Spiekerkoetter, Ute, et al.. (2023). Genomic newborn screening: Are we entering a new era of screening?. Journal of Inherited Metabolic Disease. 46(5). 778–795. 26 indexed citations

Bick, David, et al.. (2022). Newborn Screening by Genomic Sequencing: Opportunities and Challenges. International Journal of Neonatal Screening. 8(3). 40–40. 45 indexed citations

Hayeems, Robin Z., Stephanie Luca, Anna Hurst, et al.. (2022). Applying the Clinician-reported Genetic testing Utility InDEx (C-GUIDE) to genome sequencing: further evidence of validity. European Journal of Human Genetics. 30(12). 1423–1431. 9 indexed citations

Cochran, J. Nicholas, Kelly M. East, Melissa Kelly, et al.. (2021). A study of elective genome sequencing and pharmacogenetic testing in an unselected population. Molecular Genetics & Genomic Medicine. 9(9). e1766–e1766. 8 indexed citations

Marshall, Christian R., Shimul Chowdhury, Ryan J. Taft, et al.. (2020). Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease. npj Genomic Medicine. 5(1). 47–47. 85 indexed citations

Hayeems, Robin Z., David Dimmock, David Bick, et al.. (2020). Clinical utility of genomic sequencing: a measurement toolkit. npj Genomic Medicine. 5(1). 56–56. 46 indexed citations

Bick, David, et al.. (2020). An online compendium of treatable genetic disorders. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 187(1). 48–54. 43 indexed citations

10.

Zastrow, Diane B., Jennefer N. Kohler, Devon Bonner, et al.. (2019). A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing. Journal of Genetic Counseling. 28(2). 213–228. 5 indexed citations

11.

Bick, David, Marilyn C. Jones, Stacie L. Taylor, Ryan J. Taft, & John W. Belmont. (2019). Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases. Journal of Medical Genetics. 56(12). 783–791. 77 indexed citations

12.

Lu, James T., Matthew J. Ferber, Jill Hagenkord, et al.. (2018). Evaluation for Genetic Disorders in the Absence of a Clinical Indication for Testing. Journal of Molecular Diagnostics. 21(1). 3–12. 18 indexed citations

13.

Richards, Sue, Nazneen Aziz, Sherri J. Bale, et al.. (2015). Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genetics in Medicine. 17(5). 405–424. 18892 indexed citations breakdown →

14.

Samyn, Margaret M., David Bick, John A. Humphrey, & Kimberly L. Gandy. (2010). Successful Congenital Heart Surgery for a Toddler With Idiopathic Infantile Arterial Calcification. Pediatric Cardiology. 31(7). 1096–1099. 5 indexed citations

15.

Bick, David, et al.. (2008). Preimplantation HLA haplotyping using tri-, tetra-, and pentanucleotide short tandem repeats for HLA matching. Journal of Assisted Reproduction and Genetics. 25(7). 323–331. 15 indexed citations

16.

Bick, David & Eduardo C. Lau. (2006). Preimplantation Genetic Diagnosis. Pediatric Clinics of North America. 53(4). 559–577. 14 indexed citations

17.

Bhagavath, Balasubramanian, Metin Özata, I. Caglayan Ozdemír, et al.. (2005). The prevalence of gonadotropin-releasing hormone receptor mutations in a large cohort of patients with hypogonadotropic hypogonadism. Fertility and Sterility. 84(4). 951–957. 37 indexed citations

18.

Taylor, Hugh S., et al.. (1999). Mutation analysis of the EMX2 gene in Kallmann’s syndrome. Fertility and Sterility. 72(5). 910–914. 9 indexed citations

19.

Schnur, Rhonda E., et al.. (1993). Deletion Mapping and a Highly Reduced Radiation Hybrid in the Xp22.3-p22.2 Region. Genomics. 15(3). 500–506. 5 indexed citations

20.

Mahoney, M J & David Bick. (1987). Recent Advances in the Inherited Methylmalonic Acidemias. Acta Paediatrica. 76(5). 689–696. 28 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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