David Bick

43.1k citations

83 papers · 22.7k · 2 hit papers · h-index 31

Impact in

Genetics top 0.05%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
Reproductive Medicine top 0.5%
- Hypothalamic control of reproductive hormones

Papers in

Genetics 50
- Genomics and Rare Diseases 29
- Genomic variations and chromosomal abnormalities 20
- Genetics and Neurodevelopmental Disorders 7
- BRCA gene mutations in cancer 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
Molecular Biology 20

Co-authors: Heidi L. Rehm (3 shared papers)Soma Das (2 shared papers)Madhuri Hegde (2 shared papers)Elaine Lyon (3 shared papers)Sue Richards (1 shared paper)Karl V. Voelkerding (1 shared paper)Wayne W. Grody (1 shared paper)Sherri J. Bale (1 shared paper)
Journals: Fertility and Sterility (6 papers)Genetics in Medicine (5 papers)Clinical Genetics (4 papers)npj Genomic Medicine (3 papers)Prenatal Diagnosis (3 papers)
Partner nations: United States United Kingdom Canada

In The Last Decade

David Bick

81 papers receiving 22.5k citations

David Bick's Hit Papers

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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 · 19.6k citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2015 Genetics in Medicine
1989 Molecular Brain Research

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-authors

The 25 scholars most cited alongside David Bick, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with David Bick Line = papers co-authored together David Bick links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 83 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	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 ·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 Hit paper breakdown →	2015	19638
2	Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome Molecular Brain Research ·Marlene Schwanzel‐Fukuda, David Bick, Donald W. Pfaff Hit paper breakdown →	1989	451
3	Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome The American Journal of Human Genetics ·Hyung‐Goo Kim, Ingo Kurth, Fei Lan, Irene Meliciani, Wolfgang Wenzel, Soo Hyun Eom, Gil Bu Kang, Georg Rosenberger, Mustafa Tekin, Metin Özata, David Bick, Richard J. Sherins, Steven L. Walker, Yang Shi, James F. Gusella, Lawrence C. Layman	2008	237
4	Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome. Proceedings of the National Academy of Sciences ·Andrea Ballabio, Barbara Bardoni, Rosalba Carrozzo, Generoso Andria, David Bick, L. B. Campbell, Ben C.J. Hamel, M.A. Ferguson‐Smith, Giorgio Gimelli, M. Fraccaro	1989	200
5	Intragenic Deletion of theKALIG-1Gene in Kallmann's Syndrome New England Journal of Medicine ·David Bick, Brunella Franco, Richard J. Sherins, Babette Heye, Lisa Pike, John M. Crawford, Anne Maddalena, Barbara Incerti, Antonella Pragliola, Thomas Meitinger, Andrea Ballabio	1992	141
6	Whole exome and whole genome sequencing Current Opinion in Pediatrics ·David Bick, David Dimmock	2011	108
7	Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease 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	2020	89
8	Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases Journal of Medical Genetics ·David Bick, Marilyn C. Jones, Stacie L. Taylor, Ryan J. Taft, John W. Belmont	2019	80
9	Next-generation sequencing for constitutional variants in the clinical laboratory, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG) Genetics in Medicine ·Catherine Rehder, Lora Jh Bean, David Bick, Elizabeth Chao, Wendy K. Chung, Soma Das, Julianne O’Daniel, Heidi L. Rehm, Vandana Shashi, Lisa M. Vincent	2021	78
10	Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism Fertility and Sterility ·Balasubramanian Bhagavath, Robert H. Podolsky, Metin Özata, Erol Bolu, David Bick, Anita S. Kulharya, Richard J. Sherins, Lawrence C. Layman	2006	78
11	The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome Fertility and Sterility ·Samuel D. Quaynor, Hyung‐Goo Kim, Elizabeth M. Cappello, Tiera Williams, Lynn P. Chorich, David Bick, Richard J. Sherins, Lawrence C. Layman	2011	76
12	Human gene copy number spectra analysis in congenital heart malformations Physiological Genomics ·Aoy Tomita‐Mitchell, Donna K. Mahnke, Craig A. Struble, Maureen E. Tuffnell, Karl Stamm, Mats Hidestrand, Susan E. Harris, Mary Goetsch, Pippa Simpson, David Bick, Ulrich Broeckel, Andrew N. Pelech, James S. Tweddell, Michael E. Mitchell	2012	74
13	Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey study Clinical Genetics ·AA Lemke, David Bick, David Dimmock, Pippa Simpson, Regan Veith	2012	64
14	Mutational Analysis of DAX1 in Patients with Hypogonadotropic Hypogonadism or Pubertal Delay1 The Journal of Clinical Endocrinology & Metabolism ·John C. Achermann, Wen-Xia Gu, T J Kotlar, Joshua J. Meeks, Leah Sabacan, Stephanie B. Seminara, Reema L. Habiby, Peter C. Hindmarsh, David Bick, Richard J. Sherins, William F. Crowley, Lawrence C. Layman, J. Larry Jameson	1999	60
15	Differential expression of novel Gsα signal transduction protein cDNA species Nucleic Acids Research ·Anand Swaroop, Neeraj Agarwal, Jeffrey R. Gruen, David Bick, Sherman M. Weissman	1991	58
16	Brief Report Obstetrical & Gynecological Survey ·David Bick, Brunella Franco, Richard J. Sherins, Babette Heye, Lisa Pike, John M. Crawford, Anne Maddalena, Barbara Incerti, Antonella Pragliola, Thomas Meitinger, Andrea Ballabio	1992	58
17	Male infant with ichthyosis, Kallmann syndrome, chondrodysplasia punctata, and an Xp chromosome deletion American Journal of Medical Genetics ·David Bick, Cynthia J. Curry, J. McGill, Daniel F. Schorderet, Robert C. Bux, Charleen M. Moore	1989	56
18	Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States Molecular Genetics and Metabolism ·Marcus J. Miller, Lindsay C. Burrage, James B. Gibson, Meghan E. Strenk, Edward J. Lose, David Bick, Sarah H. Elsea, V. Reid Sutton, Qin Sun, Brett H. Graham, William J. Craigen, Victor Wei Zhang, Lee-Jun Wong	2015	53
19	The prevalence of intragenic deletions in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome Molecular Human Reproduction ·Jennifer Pedersen-White, Lynn P. Chorich, David Bick, Richard J. Sherins, Lawrence C. Layman	2008	50
20	Clinical utility of genomic sequencing: a measurement toolkit npj Genomic Medicine ·Robin Z. Hayeems, David Dimmock, David Bick, John W. Belmont, Robert C. Green, Brendan C. Lanpher, Vaidehi Jobanputra, Roberto Mendoza‐Londono, Shashi Kulkarni, Megan E. Grove, Stacie L. Taylor, Euan A. Ashley	2020	48

About David Bick

David Bick is a scholar working on Genetics, Molecular Biology, Reproductive Medicine, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health, having authored 83 papers that have together received 22.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (29 papers), Genomic variations and chromosomal abnormalities (20 papers), Hypothalamic control of reproductive hormones (11 papers), Genetic factors in colorectal cancer (10 papers), Prenatal Screening and Diagnostics (9 papers), Genetics and Neurodevelopmental Disorders (7 papers), BRCA gene mutations in cancer (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). The work is most often cited by research in Genetics (8.4k citations), Reproductive Medicine (1.2k citations), Clinical Biochemistry (863 citations), Genetics (1.3k citations) and Molecular Biology (8.1k citations). David Bick has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Heidi L. Rehm, Soma Das, Madhuri Hegde, Elaine Lyon, Sue Richards, Karl V. Voelkerding, Wayne W. Grody, Sherri J. Bale, Elaine Spector and Julie M. Gastier‐Foster. Their work appears in journals such as Fertility and Sterility, Genetics in Medicine, Clinical Genetics, npj Genomic Medicine and Prenatal Diagnosis.

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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