For researchers
Is your paper here?
2,671 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
14 matches for
Ali M.
Association analysis in over 329,000 individuals identifies 116 independent variants influencing neuroticism
Luciano M,
Hagenaars SP,
Davies G,
Hill WD,
Clarke TK,
Shirali M,
Harris SE,
Marioni RE,
Liewald DC,
Fawns-Ritchie C,
Adams MJ,
Howard DM
and 4 more — show all
Nature genetics · 2018 · PMID 29255261
12 pages+
Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways
Howard DM,
Adams MJ,
Shirali M,
Clarke TK,
Marioni RE,
Davies G,
Coleman JRI,
Alloza C,
Shen X,
Barbu MC,
Wigmore EM,
Gibson J
and 9 more — show all
23andMe Research Team
Nature communications · 2018 · PMID 29662059 · open access
12 pages+
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
Howard DM,
Adams MJ,
Clarke TK,
Hafferty JD,
Gibson J,
Shirali M,
Coleman JRI,
Hagenaars SP,
Ward J,
Wigmore EM,
Alloza C,
Shen X
and 26 more — show all
Barbu MC,
Xu EY,
Whalley HC,
Marioni RE,
Porteous DJ,
Davies G,
Deary IJ,
Hemani G,
Berger K,
Teismann H,
Rawal R,
Arolt V,
Baune BT,
Dannlowski U,
Domschke K,
Tian C,
Hinds DA,
Trzaskowski M,
Byrne EM,
Ripke S,
Smith DJ,
Sullivan PF,
Wray NR,
Breen G,
Lewis CM,
McIntosh AM
23andMe Research Team · Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Nature neuroscience · 2019 · PMID 30718901
12 pages+
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus
Hardcastle AJ,
Liskova P,
Bykhovskaya Y,
McComish BJ,
Davidson AE,
Inglehearn CF,
Li X,
Choquet H,
Habeeb M,
Lucas SEM,
Sahebjada S,
Pontikos N
and 50 more — show all
Lopez KER,
Khawaja AP,
Ali M,
Dudakova L,
Skalicka P,
Van Dooren BTH,
Geerards AJM,
Haudum CW,
Faro VL,
Tenen A,
Simcoe MJ,
Patasova K,
Yarrand D,
Yin J,
Siddiqui S,
Rice A,
Farraj LA,
Chen YI,
Rahi JS,
Krauss RM,
Theusch E,
Charlesworth JC,
Szczotka-Flynn L,
Toomes C,
Meester-Smoor MA,
Richardson AJ,
Mitchell PA,
Taylor KD,
Melles RB,
Aldave AJ,
Mills RA,
Cao K,
Chan E,
Daniell MD,
Wang JJ,
Rotter JI,
Hewitt AW,
MacGregor S,
Klaver CCW,
Ramdas WD,
Craig JE,
Iyengar SK,
O'Brart D,
Jorgenson E,
Baird PN,
Rabinowitz YS,
Burdon KP,
Hammond CJ,
Tuft SJ,
Hysi PG
Communications biology · 2021 · PMID 33649486 · open access
12 pages+
Proteogenomic analysis of human cerebrospinal fluid identifies neurologically relevant regulation and implicates causal proteins for Alzheimer's disease
Western D,
Timsina J,
Wang L,
Wang C,
Yang C,
Phillips B,
Wang Y,
Liu M,
Ali M,
Beric A,
Gorijala P,
Kohlfeld P
and 28 more — show all
Budde J,
Levey AI,
Morris JC,
Perrin RJ,
Ruiz A,
Marquié M,
Boada M,
de Rojas I,
Rutledge J,
Oh H,
Wilson EN,
Le Guen Y,
Reus LM,
Tijms B,
Visser PJ,
van der Lee SJ,
Pijnenburg YAL,
Teunissen CE,
Del Campo Milan M,
Alvarez I,
Aguilar M,
Greicius MD,
Pastor P,
Pulford DJ,
Ibanez L,
Wyss-Coray T,
Sung YJ,
Cruchaga C
Dominantly Inherited Alzheimer Network (DIAN) · Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Nature genetics · 2024 · PMID 39528825
12 pages+
Genetic architecture of cerebrospinal fluid and brain metabolite levels and the genetic colocalization of metabolites with human traits
Wang C,
Yang C,
Western D,
Ali M,
Wang Y,
Phuah CL,
Budde J,
Wang L,
Gorijala P,
Timsina J,
Ruiz A,
Pastor P
and 14 more — show all
Fernandez MV,
Panyard DJ,
Engelman CD,
Deming Y,
Boada M,
Cano A,
Garcia-Gonzalez P,
Graff-Radford NR,
Mori H,
Lee JH,
Perrin RJ,
Ibanez L,
Sung YJ,
Cruchaga C
Dominantly Inherited Alzheimer Network (DIAN) · Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Nature genetics · 2024 · PMID 39528826
12 pages+
Genome-wide association study identifies multiple susceptibility loci for multiple myeloma
Mitchell JS,
Li N,
Weinhold N,
Försti A,
Ali M,
van Duin M,
Thorleifsson G,
Johnson DC,
Johnson DC,
Chen B,
Halvarsson BM,
Gudbjartsson DF
and 47 more — show all
Kuiper R,
Stephens OW,
Bertsch U,
Broderick P,
Campo C,
Einsele H,
Gregory WA,
Gullberg U,
Henrion M,
Hillengass J,
Hoffmann P,
Jackson GH,
Johnsson E,
Jöud M,
Kristinsson SY,
Lenhoff S,
Lenive O,
Mellqvist UH,
Migliorini G,
Nahi H,
Nelander S,
Nickel J,
Nöthen MM,
Rafnar T,
Ross FM,
da Silva Filho MI,
Swaminathan B,
Thomsen H,
Turesson I,
Vangsted A,
Vogel U,
Waage A,
Walker BA,
Wihlborg AK,
Broyl A,
Davies FE,
Thorsteinsdottir U,
Langer C,
Hansson M,
Kaiser M,
Sonneveld P,
Stefansson K,
Morgan GJ,
Goldschmidt H,
Hemminki K,
Nilsson B,
Houlston RS
Nature communications · 2016 · PMID 27363682 · open access
9 pages
Identification of sequence variants influencing immunoglobulin levels
Jonsson S,
Sveinbjornsson G,
de Lapuente Portilla AL,
Swaminathan B,
Plomp R,
Dekkers G,
Ajore R,
Ali M,
Bentlage AEH,
Elmér E,
Eyjolfsson GI,
Gudjonsson SA
and 26 more — show all
Gullberg U,
Gylfason A,
Halldorsson BV,
Hansson M,
Holm H,
Johansson Å,
Johnsson E,
Jonasdottir A,
Ludviksson BR,
Oddsson A,
Olafsson I,
Olafsson S,
Sigurdardottir O,
Sigurdsson A,
Stefansdottir L,
Masson G,
Sulem P,
Wuhrer M,
Wihlborg AK,
Thorleifsson G,
Gudbjartsson DF,
Thorsteinsdottir U,
Vidarsson G,
Jonsdottir I,
Nilsson B,
Stefansson K
Nature genetics · 2017 · PMID 28628107
6 pages
Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma
Went M,
Sud A,
Försti A,
Halvarsson BM,
Weinhold N,
Kimber S,
van Duin M,
Thorleifsson G,
Holroyd A,
Johnson DC,
Johnson DC,
Li N
and 58 more — show all
Orlando G,
Law PJ,
Ali M,
Chen B,
Mitchell JS,
Gudbjartsson DF,
Kuiper R,
Stephens OW,
Bertsch U,
Broderick P,
Campo C,
Bandapalli OR,
Einsele H,
Gregory WA,
Gullberg U,
Hillengass J,
Hoffmann P,
Jackson GH,
Jöckel KH,
Johnsson E,
Kristinsson SY,
Mellqvist UH,
Nahi H,
Easton D,
Pharoah P,
Dunning A,
Peto J,
Canzian F,
Swerdlow A,
Eeles RA,
Kote-Jarai Z,
Muir K,
Pashayan N,
Nickel J,
Nöthen MM,
Rafnar T,
Ross FM,
da Silva Filho MI,
Thomsen H,
Turesson I,
Vangsted A,
Andersen NF,
Waage A,
Walker BA,
Wihlborg AK,
Broyl A,
Davies FE,
Thorsteinsdottir U,
Langer C,
Hansson M,
Goldschmidt H,
Kaiser M,
Sonneveld P,
Stefansson K,
Morgan GJ,
Hemminki K,
Nilsson B,
Houlston RS
PRACTICAL consortium
Nature communications · 2018 · PMID 30213928 · open access
5 pages
Proteo-genomics of soluble TREM2 in cerebrospinal fluid provides novel insights and identifies novel modulators for Alzheimer's disease
Wang L,
Nykänen NP,
Western D,
Gorijala P,
Timsina J,
Li F,
Wang Z,
Ali M,
Yang C,
Liu M,
Brock W,
Marquié M
and 21 more — show all
Boada M,
Alvarez I,
Aguilar M,
Pastor P,
Ruiz A,
Puerta R,
Orellana A,
Rutledge J,
Oh H,
Greicius MD,
Le Guen Y,
Perrin RJ,
Wyss-Coray T,
Jefferson A,
Hohman TJ,
Graff-Radford N,
Mori H,
Goate A,
Levin J,
Sung YJ,
Cruchaga C
Molecular neurodegeneration · 2024 · PMID 38172904 · open access
4 pages
GWAS meta-analysis of cerebrospinal fluid Alzheimer's biomarkers reveals loci regulating lipids, brain volume and autophagy
Timsina J,
Jiang C,
McCartney DL,
Tao F,
Dalmasso MC,
Najar J,
Anastasi F,
Ohlei O,
Puerta Fuentes R,
Yang C,
Bradley J,
Western D
and 143 more — show all
Ali M,
Wang C,
Yang C,
Wu Y,
Liu M,
Budde J,
Williams J,
Mahoney R,
Castillo Morales A,
Hohman TJ,
Dumitrescu L,
Wang TC,
Tesi N,
Kern S,
Waern M,
Skoog I,
van Harten A,
Pijnenburg YAL,
van der Flier WM,
Sánchez-Juan P,
Rodriguez-Rodriguez E,
Kleineidam L,
Peters O,
Schneider A,
Küçükali F,
Bellenguez C,
Grenier-Boley B,
Heikkinen S,
de Rojas I,
Rujescu D,
Scherbaum N,
Hausner L,
Düzel E,
Grimmer T,
Wiltfang J,
Vandenberghe R,
Engelborghs S,
Heilmann-Heimbach S,
Schmid M,
Tegos T,
Scarmeas N,
Dols-Icardo O,
Moreno F,
Pérez-Tur J,
Bullido MJ,
Sánchez-Valle R,
Álvarez V,
García-González P,
Mir P,
Real LM,
Piñol-Ripoll G,
García-Alberca JM,
Seelaar H,
Ramakers I,
Papma J,
Hulsman M,
Laske C,
Teipel S,
Priller J,
Perneczky R,
Buerger K,
Nöthen MM,
Lewczuk P,
Kornhuber J,
Hampel H,
Giegling I,
Goldhardt O,
Diehl-Schmid J,
Andrade V,
Heneka MM,
Frölich L,
Vogelgsang J,
Graff C,
Thonberg H,
Ullgren A,
Papenberg G,
Deleuze JF,
Dufouil C,
Wagner M,
Jessen F,
Holstege H,
van Duijn C,
Lebouvier T,
Hannon O,
Leinonen V,
Soininen H,
Herukka SK,
Giedraitis V,
Löwenmark M,
Kilander L,
Genius P,
Rodríguez B,
Luckett ES,
Navarro A,
Cano A,
Marquié M,
Blennow K,
Zetterberg H,
Lleo A,
Boada M,
Ruiz A,
Lee VM,
Van Deerlin VM,
Deming Y,
Johnson SC,
Engelman CD,
Pastor P,
Alvarez I,
Peskind ER,
Heslegrave AJ,
Saykin AJ,
Nho K,
Schindler SE,
Morris JC,
Holtzman DM,
McDade E,
Renton AE,
Goate A,
Ibanez L,
Riemenschneider M,
Albert MS,
Laws SM,
Porter T,
O'Brien EK,
Shaw LM,
Tijms BM,
Ingelsson M,
Visser PJ,
Hiltunen M,
Sleegers K,
Ritchie CW,
Sims R,
Belloy M,
Lambert JC,
Vilor-Tejedor N,
Fernández MV,
Li QS,
Nagle MW,
Marioni RE,
Ramirez A,
Bertram L,
van der Lee SJ,
Cruchaga C
Nature communications · 2026 · PMID 42014397 · open access
4 pages
Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers
Jansen IE,
van der Lee SJ,
Gomez-Fonseca D,
de Rojas I,
Dalmasso MC,
Grenier-Boley B,
Zettergren A,
Mishra A,
Ali M,
Andrade V,
Bellenguez C,
Kleineidam L
and 134 more — show all
Küçükali F,
Sung YJ,
Tesí N,
Vromen EM,
Wightman DP,
Alcolea D,
Alegret M,
Alvarez I,
Amouyel P,
Athanasiu L,
Bahrami S,
Bailly H,
Belbin O,
Bergh S,
Bertram L,
Biessels GJ,
Blennow K,
Blesa R,
Boada M,
Boland A,
Buerger K,
Carracedo Á,
Cervera-Carles L,
Chene G,
Claassen JAHR,
Debette S,
Deleuze JF,
de Deyn PP,
Diehl-Schmid J,
Djurovic S,
Dols-Icardo O,
Dufouil C,
Duron E,
Düzel E,
Fladby T,
Fortea J,
Frölich L,
García-González P,
Garcia-Martinez M,
Giegling I,
Goldhardt O,
Gobom J,
Grimmer T,
Haapasalo A,
Hampel H,
Hanon O,
Hausner L,
Heilmann-Heimbach S,
Helisalmi S,
Heneka MT,
Hernández I,
Herukka SK,
Holstege H,
Jarholm J,
Kern S,
Knapskog AB,
Koivisto AM,
Kornhuber J,
Kuulasmaa T,
Lage C,
Laske C,
Leinonen V,
Lewczuk P,
Lleó A,
de Munain AL,
Lopez-Garcia S,
Maier W,
Marquié M,
Mol MO,
Montrreal L,
Moreno F,
Moreno-Grau S,
Nicolas G,
Nöthen MM,
Orellana A,
Pålhaugen L,
Papma JM,
Pasquier F,
Perneczky R,
Peters O,
Pijnenburg YAL,
Popp J,
Posthuma D,
Pozueta A,
Priller J,
Puerta R,
Quintela I,
Ramakers I,
Rodriguez-Rodriguez E,
Rujescu D,
Saltvedt I,
Sanchez-Juan P,
Scheltens P,
Scherbaum N,
Schmid M,
Schneider A,
Selbæk G,
Selnes P,
Shadrin A,
Skoog I,
Soininen H,
Tárraga L,
Teipel S,
Tijms B,
Tsolaki M,
Van Broeckhoven C,
Van Dongen J,
van Swieten JC,
Vandenberghe R,
Vidal JS,
Visser PJ,
Vogelgsang J,
Waern M,
Wagner M,
Wiltfang J,
Wittens MMJ,
Zetterberg H,
Zulaica M,
van Duijn CM,
Bjerke M,
Engelborghs S,
Jessen F,
Teunissen CE,
Pastor P,
Hiltunen M,
Ingelsson M,
Andreassen OA,
Clarimón J,
Sleegers K,
Ruiz A,
Ramirez A,
Cruchaga C,
Lambert JC,
van der Flier W
EADB consortium · GR@ACE study group
Acta neuropathologica · 2022 · PMID 36066633 · open access
3 pages
A study assessing the association of glycated hemoglobin A1C (HbA1C) associated variants with HbA1C, chronic kidney disease and diabetic retinopathy in populations of Asian ancestry
Chen P,
Ong RT,
Tay WT,
Sim X,
Ali M,
Xu H,
Suo C,
Liu J,
Chia KS,
Vithana E,
Young TL,
Aung T
and 6 more — show all
PloS one · 2013 · PMID 24244560 · open access
1 page
Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma
Swaminathan B,
Thorleifsson G,
Jöud M,
Ali M,
Johnsson E,
Ajore R,
Sulem P,
Halvarsson BM,
Eyjolfsson G,
Haraldsdottir V,
Hultman C,
Ingelsson E
and 22 more — show all
Kristinsson SY,
Kähler AK,
Lenhoff S,
Masson G,
Mellqvist UH,
Månsson R,
Nelander S,
Olafsson I,
Sigurðardottir O,
Steingrimsdóttir H,
Vangsted A,
Vogel U,
Waage A,
Nahi H,
Gudbjartsson DF,
Rafnar T,
Turesson I,
Gullberg U,
Stefánsson K,
Hansson M,
Thorsteinsdóttir U,
Nilsson B
Nature communications · 2015 · PMID 26007630 · open access
1 page
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.