Ian D. Krantz

22.7k total citations · 3 hit papers
161 papers, 8.3k citations indexed

About

Ian D. Krantz is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Ian D. Krantz has authored 161 papers receiving a total of 8.3k indexed citations (citations by other indexed papers that have themselves been cited), including 90 papers in Molecular Biology, 67 papers in Genetics and 42 papers in Surgery. Recurrent topics in Ian D. Krantz's work include Genomics and Chromatin Dynamics (44 papers), Genomic variations and chromosomal abnormalities (35 papers) and Pediatric Hepatobiliary Diseases and Treatments (32 papers). Ian D. Krantz is often cited by papers focused on Genomics and Chromatin Dynamics (44 papers), Genomic variations and chromosomal abnormalities (35 papers) and Pediatric Hepatobiliary Diseases and Treatments (32 papers). Ian D. Krantz collaborates with scholars based in United States, Italy and Canada. Ian D. Krantz's co-authors include Nancy B. Spinner, David A. Piccoli, Håkon Håkonarson, Kai Wang, David B. Goldstein, Samuel P. Dickson, Anna Genin, Laird G. Jackson, Matthew A. Deardorff and Binita M. Kamath and has published in prestigious journals such as Nucleic Acids Research, Circulation and Nature Medicine.

In The Last Decade

Ian D. Krantz

159 papers receiving 8.1k 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.

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

1997 801 citations Ian D. Krantz, David A. Piccoli et al. profile →
Rare Variants Create Synthetic Genome-Wide Associations

2010 611 citations Kai Wang, Ian D. Krantz et al. profile →
NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway

2006 489 citations Ian D. Krantz, David A. Piccoli et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ian D. Krantz United States	45	4.3k	3.1k	2.1k	1.3k	784	161	8.3k
Alain Verloès France	46	4.4k 1.0×	3.8k 1.2×	1.1k 0.5×	1.0k 0.8×	807 1.0×	314	8.7k
Didier Lacombe France	48	4.0k 0.9×	2.7k 0.9×	1.1k 0.5×	791 0.6×	819 1.0×	322	7.8k
Nancy B. Spinner United States	53	4.9k 1.1×	4.0k 1.3×	4.0k 1.9×	2.4k 1.8×	1.3k 1.7×	186	11.2k
David Chitayat Canada	55	4.8k 1.1×	3.3k 1.1×	1.9k 0.9×	867 0.7×	3.1k 3.9×	403	11.6k
Anita Rauch Germany	48	4.4k 1.0×	3.4k 1.1×	617 0.3×	509 0.4×	679 0.9×	194	7.5k
Erik G. Puffenberger United States	38	2.8k 0.6×	2.9k 0.9×	1.3k 0.6×	978 0.7×	413 0.5×	74	6.7k
Isabella Ceccherini Italy	44	3.8k 0.9×	1.6k 0.5×	2.5k 1.2×	1.0k 0.8×	350 0.4×	232	8.1k
Koenraad Devriendt Belgium	56	6.8k 1.6×	6.0k 1.9×	1.5k 0.7×	1.5k 1.1×	1.8k 2.4×	444	12.6k
Valérie Cormier‐Daire France	62	8.4k 1.9×	7.2k 2.3×	1.3k 0.6×	1.2k 0.9×	1.0k 1.3×	393	14.3k
Angela E. Lin United States	48	3.0k 0.7×	2.7k 0.9×	2.1k 1.0×	1.9k 1.4×	1.3k 1.6×	190	8.6k

Countries citing papers authored by Ian D. Krantz

Since Specialization

Citations

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

Fields of papers citing papers by Ian D. Krantz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ian D. Krantz. 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 Ian D. Krantz. The network helps show where Ian D. Krantz may publish in the future.

Co-authorship network of co-authors of Ian D. Krantz

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

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

Medne, Līvija, Cara Skraban, Christopher Gray, et al.. (2023). Retrospective identification of patients with SRRM2‐related neurodevelopmental disorder in a single tertiary children's hospital. American Journal of Medical Genetics Part A. 191(8). 2149–2155. 3 indexed citations

Deniz, Engin, Weidong Ji, Monica Konstantino, et al.. (2023). CFAP45, a heterotaxy and congenital heart disease gene, affects cilia stability. Developmental Biology. 499. 75–88. 7 indexed citations

Wild, K. Taylor, Deborah McEldrew, Maninder Kaur, et al.. (2022). Molecular Mechanisms Contributing to the Etiology of Congenital Diaphragmatic Hernia: A Review and Novel Cases. The Journal of Pediatrics. 246. 251–265.e2. 3 indexed citations

Wild, K. Taylor, Erica Schindewolf, Holly L. Hedrick, et al.. (2022). The Genomics of Congenital Diaphragmatic Hernia: A 10-Year Retrospective Review. The Journal of Pediatrics. 248. 108–113.e2. 8 indexed citations

Havrilla, James M., et al.. (2022). PheNominal: an EHR-integrated web application for structured deep phenotyping at the point of care. BMC Medical Informatics and Decision Making. 22(S2). 198–198. 6 indexed citations

Strong, Alanna, Dong Li, Frank Mentch, et al.. (2020). Ciliopathies: Coloring outside of the lines. American Journal of Medical Genetics Part A. 185(3). 687–694. 7 indexed citations

Ritter, Alyssa, Emma Bedoukian, Justin H. Berger, et al.. (2019). Clinical utility of exome sequencing in infantile heart failure. Genetics in Medicine. 22(2). 423–426. 13 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

10.

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

11.

Noon, Sarah E., E Schwartz, Alisha Wilkens, et al.. (2016). Outcomes of evaluation and testing of 660 individuals with hearing loss in a pediatric genetics of hearing loss clinic. American Journal of Medical Genetics Part A. 170(10). 2523–2530. 36 indexed citations

12.

Mannini, Linda, Francesco Cucco, Valentina Quarantotti, et al.. (2015). SMC1B is present in mammalian somatic cells and interacts with mitotic cohesin proteins. Scientific Reports. 5(1). 18472–18472. 26 indexed citations

13.

Izumi, Kosuke & Ian D. Krantz. (2014). Pallister–Killian syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 166(4). 406–413. 43 indexed citations

14.

Kamath, Binita M., Robert C. Bauer, Kathleen M. Loomes, et al.. (2011). NOTCH2 mutations in Alagille syndrome. Journal of Medical Genetics. 49(2). 138–144. 149 indexed citations

15.

Hennekam, Raoul C. M., Ian D. Krantz, & Judith Allanson. (2010). Gorlin's Syndromes of the Head and Neck. Data Archiving and Networked Services (DANS). 140 indexed citations

16.

Gibbons, Richard J., Takahito Wada, Christopher A. Fisher, et al.. (2008). Mutations in the chromatin-associated protein ATRX. Human Mutation. 29(6). 796–802. 125 indexed citations

17.

Liu, Jinglan & Ian D. Krantz. (2008). Cohesin and Human Disease. Annual Review of Genomics and Human Genetics. 9(1). 303–320. 104 indexed citations

18.

Krantz, Ian D. & Nancy B. Spinner. (2007). Novel microdeletion syndromes. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 145C(4). 323–326. 4 indexed citations

19.

Kamath, Binita M., Kathleen M. Loomes, David A. Piccoli, et al.. (2004). Facial features in Alagille syndrome. American Journal of Medical Genetics Part A. 222–223. 4 indexed citations

20.

Krantz, Ian D., David A. Piccoli, & Nancy B. Spinner. (1997). Alagille syndrome.. Journal of Medical Genetics. 34(2). 152–157. 117 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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