SMAD5 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "SMAD5" in English language version.

Last modified: 14:22:03, 26 July 2026 (UTC)

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630^th place

326^th place

5^th place

2^nd place

15^th place

8^th place

9,898^th place

6,429^th place

doi.org (Global: 2^nd place; English: 2^nd place)

Riggins GJ, Thiagalingam S, Rozenblum E, Weinstein CL, Kern SE, Hamilton SR, Willson JK, Markowitz SD, Kinzler KW, Vogelstein B (July 1996). "Mad-related genes in the human". Nat. Genet. 13 (3): 347–9. doi:10.1038/ng0796-347. PMID 8673135. S2CID 10124489.
Alankarage D, Leshchynska I, Portelli S, Sipka A, Blue GM, O'Reilly V, Das D, Rath EM, Enriquez A, Troup M, Fine M, Poplawski N, Verlee M, Humphreys DT, Harvey RP, Chapman G, Kirk EP, Winlaw DS, Callewaert B, Chung WK, Ascher D, Giannoulatou E, Dunwoodie SL (5 July 2025). "Haploinsufficient variants in SMAD5 are associated with isolated congenital heart disease". Human Genetics and Genomics Advances. 6 (4) 100478. doi:10.1016/j.xhgg.2025.100478. PMC 12305712. PMID 40619738.

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Alankarage D, Leshchynska I, Portelli S, Sipka A, Blue GM, O'Reilly V, Das D, Rath EM, Enriquez A, Troup M, Fine M, Poplawski N, Verlee M, Humphreys DT, Harvey RP, Chapman G, Kirk EP, Winlaw DS, Callewaert B, Chung WK, Ascher D, Giannoulatou E, Dunwoodie SL (5 July 2025). "Haploinsufficient variants in SMAD5 are associated with isolated congenital heart disease". Human Genetics and Genomics Advances. 6 (4) 100478. doi:10.1016/j.xhgg.2025.100478. PMC 12305712. PMID 40619738.

Riggins GJ, Thiagalingam S, Rozenblum E, Weinstein CL, Kern SE, Hamilton SR, Willson JK, Markowitz SD, Kinzler KW, Vogelstein B (July 1996). "Mad-related genes in the human". Nat. Genet. 13 (3): 347–9. doi:10.1038/ng0796-347. PMID 8673135. S2CID 10124489.
Alankarage D, Leshchynska I, Portelli S, Sipka A, Blue GM, O'Reilly V, Das D, Rath EM, Enriquez A, Troup M, Fine M, Poplawski N, Verlee M, Humphreys DT, Harvey RP, Chapman G, Kirk EP, Winlaw DS, Callewaert B, Chung WK, Ascher D, Giannoulatou E, Dunwoodie SL (5 July 2025). "Haploinsufficient variants in SMAD5 are associated with isolated congenital heart disease". Human Genetics and Genomics Advances. 6 (4) 100478. doi:10.1016/j.xhgg.2025.100478. PMC 12305712. PMID 40619738.

Riggins GJ, Thiagalingam S, Rozenblum E, Weinstein CL, Kern SE, Hamilton SR, Willson JK, Markowitz SD, Kinzler KW, Vogelstein B (July 1996). "Mad-related genes in the human". Nat. Genet. 13 (3): 347–9. doi:10.1038/ng0796-347. PMID 8673135. S2CID 10124489.