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 Canada. David Bick's co-authors include Heidi L. Rehm, Soma Das, Madhuri Hegde, Elaine Lyon, Karl V. Voelkerding, Julie M. Gastier‐Foster, Sue Richards, Wayne W. Grody, Sherri J. Bale 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

align trajectories

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 →

Peers

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

#	Work	Indexed citations
1	Clinical and Biochemical Phenotype Across the Genotypic Spectrum of 21-hydroxylase Deficiency in 457 Individuals 2025 ·The Journal of Clinical Endocrinology & Metabolism ·Qizong Lao, Alan H. Schulman, (unknown), (unknown), David Bick, (unknown), (unknown), Deborah P. Merke	0
2	Newborn Screening by Genomic Sequencing: Opportunities and Challenges 2022 ·International Journal of Neonatal Screening ·David Bick, (unknown), (unknown), Alessandra Ferlini, (unknown), Dalia Kasperavičiūtė, (unknown), (unknown), Augusto Rendon, (unknown), (unknown), Richard H. Scott	45
3	Applying the Clinician-reported Genetic testing Utility InDEx (C-GUIDE) to genome sequencing: further evidence of validity 2022 ·European Journal of Human Genetics ·Robin Z. Hayeems, Stephanie Luca, Anna Hurst, J. Nicholas Cochran, (unknown), Alomgir Hossain, Lauren Chad, M. Stephen Meyn, Eleanor Pullenayegum, Wendy J. Ungar, David Bick	9
4	A study of elective genome sequencing and pharmacogenetic testing in an unselected population 2021 ·Molecular Genetics & Genomic Medicine ·J. Nicholas Cochran, Kelly M. East, (unknown), Melissa Kelly, Whitley V. Kelley, Troy Moore, R Myers, (unknown), Molly C. Schroeder, David Bick	8
5	Reducing Sanger confirmation testing through false positive prediction algorithms 2021 ·Genetics in Medicine ·James Holt, Melissa Kelly, (unknown), Ghunwa Nakouzi, David Bick, Elaine Lyon	9
6	Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease 2020 ·npj Genomic Medicine ·Christian R. Marshall, Shimul Chowdhury, Ryan J. Taft, Matthew S. Lebo, Jillian G. Buchan, Steven M. Harrison, Ross Rowsey, Eric W. Klee, Pengfei Liu, Elizabeth A. Worthey, Vaidehi Jobanputra, David Dimmock, Hutton M. Kearney, David Bick, Shashikant Kulkarni, Stacie L. Taylor, John W. Belmont, Dimitri J. Stavropoulos, Niall J. Lennon	85
7	Clinical utility of genomic sequencing: a measurement toolkit 2020 ·npj Genomic Medicine ·Robin Z. Hayeems, David Dimmock, David Bick, John W. Belmont, Robert C. Green, Brendan C. Lanpher, Vaidehi Jobanputra, Roberto Mendoza‐Londono, (unknown), Megan E. Grove, Stacie L. Taylor, Euan A. Ashley	46
8	An online compendium of treatable genetic disorders 2020 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·David Bick, (unknown), David Dimmock, Tom Fowler, Mark J. Caulfield, Richard H. Scott	43
9	The Medical Genome Initiative: moving whole-genome sequencing for rare disease diagnosis to the clinic 2020 ·Genome Medicine ·Christian R. Marshall, David Bick, John W. Belmont, Stacie L. Taylor, Euan A. Ashley, David Dimmock, Vaidehi Jobanputra, Hutton M. Kearney, Shashikant Kulkarni, Heidi L. Rehm	27
10	A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing 2019 ·Journal of Genetic Counseling ·Diane B. Zastrow, Jennefer N. Kohler, Devon Bonner, Chloe M. Reuter, Liliana Fernández, Megan E. Grove, Dianna G. Fisk, (unknown), Yaping Yang, Christine M. Eng, Patricia A. Ward, David Bick, Elizabeth A. Worthey, Paul G. Fisher, Euan A. Ashley, Jonathan A. Bernstein, Matthew T. Wheeler	5
11	Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases 2019 ·Journal of Medical Genetics ·David Bick, Marilyn C. Jones, Stacie L. Taylor, Ryan J. Taft, John W. Belmont	77
12	Evaluation for Genetic Disorders in the Absence of a Clinical Indication for Testing 2018 ·Journal of Molecular Diagnostics ·James T. Lu, Matthew J. Ferber, Jill Hagenkord, Elissa Levin, Sarah T. South, Hyunseok P. Kang, Kimberly A. Strong, David Bick	18
13	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 breakdown → 2015 ·Genetics in Medicine ·Sue Richards, Nazneen Aziz, Sherri J. Bale, David Bick, Soma Das, Julie M. Gastier‐Foster, Wayne W. Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector, Karl V. Voelkerding, Heidi L. Rehm	18892
14	Successful Congenital Heart Surgery for a Toddler With Idiopathic Infantile Arterial Calcification 2010 ·Pediatric Cardiology ·Margaret M. Samyn, David Bick, John A. Humphrey, Kimberly L. Gandy	5
15	Birth of a healthy infant following preimplantation PKHD1 haplotyping for autosomal recessive polycystic kidney disease using multiple displacement amplification 2010 ·Journal of Assisted Reproduction and Genetics ·Eduardo C. Lau, Marleen M. Janson, (unknown), Ellis D. Avner, Estil Strawn, David Bick	26
16	Preimplantation HLA haplotyping using tri-, tetra-, and pentanucleotide short tandem repeats for HLA matching 2008 ·Journal of Assisted Reproduction and Genetics ·(unknown), David Bick, (unknown), (unknown), Estil Strawn, Eduardo C. Lau	15
17	Preimplantation Genetic Diagnosis 2006 ·Pediatric Clinics of North America ·David Bick, Eduardo C. Lau	14
18	The prevalence of gonadotropin-releasing hormone receptor mutations in a large cohort of patients with hypogonadotropic hypogonadism 2005 ·Fertility and Sterility ·Balasubramanian Bhagavath, Metin Özata, I. Caglayan Ozdemír, Erol Bolu, David Bick, Richard J. Sherins, Lawrence C. Layman	37
19	Male infant with ichthyosis, Kallmann syndrome, chondrodysplasia punctata, and an Xp chromosome deletion 1989 ·American Journal of Medical Genetics ·David Bick, Cynthia J. Curry, J. McGill, Daniel F. Schorderet, (unknown), Charleen M. Moore	56
20	Recent Advances in the Inherited Methylmalonic Acidemias 1987 ·Acta Paediatrica ·M J Mahoney, David Bick	28

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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