Ian D. Krantz

22.7k citations
161 papers · 8.3k indexed · 3 hit papers · h-index 45
Topics
Genomics and Chromatin Dynamics (44 papers)Genomic variations and chromosomal abnormalities (35 papers)Pediatric Hepatobiliary Diseases and Treatments (32 papers)
Partner nations
United StatesItalyCanada

In The Last Decade

Ian D. Krantz

159 papers receiving 8.1k citations

Hit Papers

Mutations in the human Jagged1 gene are responsible for A...1997202620062016199720102006250500750

Peers

Ian D. Krantz
Comparison fields: 5 of 150
  • Molecular Biology 4.3k
  • Genetics 3.1k
  • Surgery 2.1k
  • Pulmonary and Respiratory Medicine 1.3k
  • Pediatrics, Perinatology and Child Health 784
Replace Nancy B. Spinner with:
Nancy B. Spinner United States
Jeanne Amiel France
David Chitayat Canada
Niklas Dahl Sweden
Richard C. Trembath United Kingdom
Carmen Ayuso Spain
Valérie Cormier‐Daire France
Elaine Spector United States
Nazneen Aziz United States
Alain Verloès France
Ian D. Krantz relative to Nancy B. Spinner United States Nancy B. Spinner's profile →
Citations per field
00.5×1.5×
Nancy B. Spinner · 1×
Citations per year

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

20 of 20 papers shown
#WorkIndexed citations
1 1
2 3
3 7
4 3
5 8
6 6
7 7
8 13
9 10
10 22
11 36
12 26
13 43
14 149
15
Gorlin's Syndromes of the Head and Neck
140
16 125
17 104
18 4
19
Facial features in Alagille syndrome
4
20 117

About Ian D. Krantz

Ian D. Krantz is a scholar working on Sensory Systems, Genetics and Developmental Biology, having authored 161 papers that have together received 8.3k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (44 papers), Genomic variations and chromosomal abnormalities (35 papers) and Pediatric Hepatobiliary Diseases and Treatments (32 papers). The work is most often cited by research in Genetics (3.1k citations), Molecular Biology (4.3k citations) and Sensory Systems (264 citations). Ian D. Krantz has collaborated with scholars based in United States, Italy and Canada. Frequent 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. Their work appears in journals such as Nucleic Acids Research, Circulation and Nature Medicine.

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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