Nicole Fleischer

1.6k total citations · 1 hit paper
18 papers, 545 citations indexed

About

Nicole Fleischer is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Nicole Fleischer has authored 18 papers receiving a total of 545 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Genetics and 3 papers in Physiology. Recurrent topics in Nicole Fleischer's work include Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (4 papers) and Lysosomal Storage Disorders Research (3 papers). Nicole Fleischer is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (4 papers) and Lysosomal Storage Disorders Research (3 papers). Nicole Fleischer collaborates with scholars based in United States, Italy and Germany. Nicole Fleischer's co-authors include Yaron Gurovich, Yair Hanani, Peter Krawitz, Lynne M. Bird, Guy Nadav, Martin Zenker, Lina Basel‐Salmon, Karen W. Gripp, Omri Bar and Susanne B. Kamphausen and has published in prestigious journals such as Nature Medicine, Human Mutation and Transactions of the Royal Society of Tropical Medicine and Hygiene.

In The Last Decade

Nicole Fleischer

16 papers receiving 525 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.

Identifying facial phenotypes of genetic disorders using deep learning

2018 411 citations Yaron Gurovich, Yair Hanani et al. Nature Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nicole Fleischer United States	9	213	172	92	57	56	18	545
Yaron Gurovich Germany	3	155 0.7×	118 0.7×	84 0.9×	54 0.9×	51 0.9×	3	440
Lina Basel‐Salmon Israel	11	285 1.3×	212 1.2×	80 0.9×	52 0.9×	52 0.9×	35	683
Yair Hanani Israel	5	154 0.7×	119 0.7×	131 1.4×	81 1.4×	52 0.9×	7	514
Omri Bar United States	8	172 0.8×	154 0.9×	95 1.0×	62 1.1×	81 1.4×	16	653
Guy Nadav Israel	6	151 0.7×	117 0.7×	88 1.0×	57 1.0×	132 2.4×	9	521
T. Beck United States	9	139 0.7×	221 1.3×	85 0.9×	7 0.1×	46 0.8×	12	566
Felipe Giuste United States	11	44 0.2×	225 1.3×	94 1.0×	13 0.2×	82 1.5×	36	519
Charis Drummer Germany	13	90 0.4×	238 1.4×	47 0.5×	31 0.5×	41 0.7×	28	510
Michael Tran Duong United States	12	34 0.2×	228 1.3×	67 0.7×	56 1.0×	201 3.6×	25	769
Angela Zhang United States	5	34 0.2×	113 0.7×	94 1.0×	16 0.3×	56 1.0×	8	503

Countries citing papers authored by Nicole Fleischer

Since Specialization

Citations

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

Fields of papers citing papers by Nicole Fleischer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicole Fleischer

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

All Works

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18 of 18 papers shown

Abdul‐Rahman, Omar, Giulia Pascolini, Giovanni Di Zenzo, et al.. (2025). Artificial Intelligence Software Changes Rare Disease Testing Strategy in Real Time: An International Case Series Using Face2Gene. American Journal of Medical Genetics Part A. 197(11). e64171–e64171.

Hirsch, Yoel, Hanna Mandel, Tova Hershkovitz, et al.. (2022). Vici syndrome in Israel: Clinical and molecular insights. Frontiers in Genetics. 13. 991721–991721.

Schmid, Alexander, Ashar Ahmad, Alexej Knaus, et al.. (2021). CADA: phenotype-driven gene prioritization based on a case-enriched knowledge graph. NAR Genomics and Bioinformatics. 3(3). lqab078–lqab078. 15 indexed citations

Mak, Bryan C., Rossana Sanchez Russo, Michael J. Gambello, et al.. (2021). Craniofacial features of 3q29 deletion syndrome: Application of next‐generation phenotyping technology. American Journal of Medical Genetics Part A. 185(7). 2094–2101. 9 indexed citations

Schneider, Holm, et al.. (2021). No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia. Orphanet Journal of Rare Diseases. 16(1). 98–98. 8 indexed citations

Fleischer, Nicole, et al.. (2021). Investigation of a dysmorphic facial phenotype in patients with Gaucher disease types 2 and 3. Molecular Genetics and Metabolism. 134(3). 274–280. 4 indexed citations

Pode‐Shakked, Ben, et al.. (2020). Shared facial phenotype of patients with mucolipidosis type IV: A clinical observation reaffirmed by next generation phenotyping. European Journal of Medical Genetics. 63(7). 103927–103927. 9 indexed citations

Pascolini, Giulia, Emanuele Agolini, Nicole Fleischer, et al.. (2020). Further delineation of the neurodevelopmental phenotypic spectrum associated to 14q11.2 microduplication. Neurological Sciences. 41(12). 3751–3753. 2 indexed citations

Pascolini, Giulia, Emanuele Agolini, Nicole Fleischer, et al.. (2020). A novel patient with White–Sutton syndrome refines the mutational and clinical repertoire of the POGZ‐related phenotype and suggests further observations. American Journal of Medical Genetics Part A. 182(7). 1791–1795. 10 indexed citations

10.

Bird, Lynne M., et al.. (2020). Differentiating molecular etiologies of Angelman syndrome through facial phenotyping using deep learning. American Journal of Medical Genetics Part A. 182(9). 2021–2026. 5 indexed citations

11.

Campos‐Xavier, Belinda, Yvonne Hilhorst‐Hofstee, Carlo Marcelis, et al.. (2020). The Connective Tissue Disorder Associated with Recessive Variants in the SLC39A13 Zinc Transporter Gene (Spondylo-Dysplastic Ehlers–Danlos Syndrome Type 3): Insights from Four Novel Patients and Follow-Up on Two Original Cases. Genes. 11(4). 420–420. 9 indexed citations

12.

Pascolini, Giulia, Nicole Fleischer, Alessandro Ferraris, Silvia Majore, & Paola Grammatico. (2019). The facial dysmorphology analysis technology in intellectual disability syndromes related to defects in the histones modifiers. Journal of Human Genetics. 64(8). 721–728. 8 indexed citations

13.

Pascolini, Giulia, Irene Bottillo, Luigi Laino, et al.. (2019). Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletion. European Journal of Medical Genetics. 63(3). 103739–103739. 5 indexed citations

14.

Carli, Diana, Elisa Giorgio, Francesca Pantaleoni, et al.. (2019). NBAS pathogenic variants: Defining the associated clinical and facial phenotype and genotype–phenotype correlations. Human Mutation. 40(6). 721–728. 15 indexed citations

15.

Gurovich, Yaron, Yair Hanani, Omri Bar, et al.. (2018). Identifying facial phenotypes of genetic disorders using deep learning. Nature Medicine. 25(1). 60–64. 411 indexed citations breakdown →

16.

Pantel, Jean Tori, Martin A. Mensah, Tzung‐Chien Hsieh, et al.. (2018). Advances in computer‐assisted syndrome recognition by the example of inborn errors of metabolism. Journal of Inherited Metabolic Disease. 41(3). 533–539. 27 indexed citations

17.

Fleischer, Nicole, et al.. (1978). [Lambliasis. Pathogenicity, clinical picture, diagnosis and therapy].. PubMed. 73(12). 415–21. 1 indexed citations

18.

Fleischer, Nicole. (1975). A study of traditional practices and early childhood anaemia in Northern Nigeria. Transactions of the Royal Society of Tropical Medicine and Hygiene. 69(2). 198–200. 7 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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