Standout Papers

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of th... 2002 2026 2010 2018 567
  1. Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family (2002)
    Karl P. Schlingmann, Stefanie Weber et al. Nature Genetics

Immediate Impact

15 by Nobel laureates 31 from Science/Nature 69 standout
Sub-graph 1 of 23

Citing Papers

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2 intermediate papers

Works of Stefanie Weber being referenced

Novel TRPM6 Mutations in 21 Families with Primary Hypomagnesemia and Secondary Hypocalcemia
2005
Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family
2002 Standout
and 1 more

Author Peers

Author Last Decade Papers Cites
Stefanie Weber 1264 1245 363 919 79 3.3k
Hiroyasu Tsukaguchi 1801 1157 294 1059 63 3.9k
Isao Matsui 1543 1602 294 457 126 4.1k
Constantine S. Anast 751 783 326 596 77 2.4k
Alkis Pierides 1648 1231 1548 243 88 3.7k
Martin Konrad 2906 1416 578 2337 96 6.1k
Nati Hernando 1527 2307 1138 1209 84 3.7k
Janet M. Canterbury 616 1675 570 433 42 2.9k
Robert Kleta 2770 1098 498 338 146 5.5k
René St‐Arnaud 2558 882 1115 693 140 5.9k
Gerti Stange 1683 1300 627 747 56 2.9k

All Works

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