Nikhil Milind

Pre-Prints

Year	Citation	DOI
2025	Gerlach PA^†, Milind N^†*, Spence JP^†, Pritchard JK^†. High false sign rates in transcriptome-wide association studies. 2025. bioRxiv*.
2025	Judd J^†, Spence JP^†, Milind N, Kachuri L, Witte JS, Pritchard JK^†. Allele frequencies at recessive disease genes are mainly determined by pleiotropic effects in heterozygotes. 2025. bioRxiv.
2024	Milind N^†, Smith CJ, Zhu H, Gjorgjieva T, Spence JP^†, Pritchard JK^†. Buffering and non-monotonic behavior of gene dosage response curves for human complex traits. 2024. medRxiv.

Year	Citation	DOI
2025	Ota M^†, Spence JP, Zeng T, ..., Milind N, Marson A^†, Pritchard JK^†. Causal modelling of gene effects from regulators to programs to traits. 2025. Nature.
2025	Spence JP^†, Mostafavi H^†, Ota M^†, Milind N, ..., Simons YB, Sella G, Pritchard JK^†. Specificity, length and luck drive gene rankings in association studies. 2025. Nature.
2024	Burnham KL, Milind N, Lee W, ..., Hinds CJ, Knight JC^†, Davenport EE^†. eQTLs identify regulatory networks and drivers of variation in the individual response to sepsis. 2024. Cell Genomics.
2020	Milind N^, Preuss C^, Haber A, ..., Logsdon BA, Crane PK, Carter GW^†. Transcriptomic stratification of late-onset Alzheimer's cases reveals novel genetic modifiers of disease pathology. 2020. PLOS Genetics.

* Equal Contribution
† Corresponding Authors