A Meindl

3.0k citations
33 papers · 2.4k · 1 hit paper · h-index 15

Impact in

  • Nephrology top 1%
    • Parathyroid Disorders and Treatments
    • Osteomyelitis and Bone Disorders Research

Papers in

    • BRCA gene mutations in cancer 11
    • Genetics and Neurodevelopmental Disorders 1
    • Immunodeficiency and Autoimmune Disorders 5

A Meindl

31 papers receiving 2.3k citations

A Meindl's Hit Papers

A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets 1995 · 944 citations
9440+10+20Years since publication250500750

Peers

A Meindl
Comparison fields: 5 of 51
  • Nephrology 650
  • Rheumatology 327
  • Immunology 160
  • Molecular Biology 521
  • Genetics 172
Replace Yasuyoshi Ueki with:
Yasuyoshi Ueki United States
Cheryl K.H. Johnson United States
Georgina Caruana Australia
Agnieszka Bierżyńska United Kingdom
Bo Åkerström Sweden
Yanyan Qian China
Evan B Der United States
Jinzhao Wang United States
D.A. Miller United States
Cécile Notarnicola France
A Meindl relative to Yasuyoshi Ueki United States Yasuyoshi Ueki's profile →
Citations per field
00.5×2×4×6×8.4×
Yasuyoshi Ueki · 1×
Citations per year

Countries citing papers authored by A Meindl

Since Specialization
Citations

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

Fields of papers citing papers by A Meindl

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside A Meindl, 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 A Meindl Line = papers co-authored together A Meindl links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 33 papers — load more, or switch the sort, to bring in the rest.

#Work
1
A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets
Hit paper breakdown →
1995944
2 1996435
3 2006363
4 1992205
5 199990
6 199676
7 199959
8 199738
9 200224
10 201224
11 199620
12 200919
13 199317
14 199917
15 201116
16 200414
17 200813
18 200912
19 201310
20 20059

About A Meindl

A Meindl is a scholar working on Genetics, Immunology, Rheumatology, Pharmacology and Nephrology, having authored 33 papers that have together received 2.4k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (11 papers), Immunodeficiency and Autoimmune Disorders (5 papers), Retinal Development and Disorders (2 papers), Genetics and Neurodevelopmental Disorders (1 paper), PI3K/AKT/mTOR signaling in cancer (1 paper), Pharmacogenetics and Drug Metabolism (1 paper), Osteomyelitis and Bone Disorders Research (1 paper) and Parathyroid Disorders and Treatments (1 paper). The work is most often cited by research in Nephrology (650 citations), Rheumatology (327 citations), Immunology (160 citations), Molecular Biology (521 citations) and Genetics (172 citations). A Meindl has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include B. H. Belohradsky, Heide Hellebrand, Thomas Meitinger, Karl Otto Schneider, Ellen D. Renner, Volkmar Jansson, Annette Friederike Jansson, Miroslav Habán, Veit Grote and Juliane Ramser. Their work appears in journals such as British Journal of Cancer, Nature Genetics, Clinical Genetics, Human Genetics and Disease Markers.

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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