Inventor · disambiguated record
Richard P. Lifton
Also filed as: LIFTON RICHARD · LIFTON RICHARD P
15 granted patents·4 pending applications·113 citations·filing 1992–2020
91Inventor score
Top patents by PatentIndex Score
19 records- 0183US10696729B2Loss of function mutations in KCNJ10 cause SeSAME, a human syndrome with sensory, neurological, and renal deficitsUNIV YALE·Filed 2017·Granted Jun 30, 2020·2 cites·10 claims
- 0279US9732138B2Loss of function mutations in KCNJ10 cause SeSAME, a human syndrome with sensory, neurological, and renal deficitsLIFTON RICHARD P·Filed 2011·Granted Aug 15, 2017·3 cites·8 claims
- 0371US5374525AMethods to determine predisposition to hypertension and association of variant angiotensinogen gene and hypertensionUNIV UTAH RES FOUND·Filed 1992·Granted Dec 20, 1994·41 cites·21 claims
- 0469US12116394B2Loss of function mutations in KCNJ10 cause SeSAME, a human syndrome with sensory, neurological, and renal deficitsUNIV YALE·Filed 2020·Granted Oct 15, 2024·0 cites·6 claims
- 0565US5589584AAngiotensinogen gene variants and predisposition to hypertensionUNIV UTAH RES FOUND·Filed 1994·Granted Dec 31, 1996·23 cites·3 claims
- 0663US6165727AMethod to determine predisposition to hypertensionUNIV UTAH RES FOUND·Filed 1999·Granted Dec 26, 2000·16 cites·2 claims
- 0761US5763168AMethod to determine predisposition to hypertensionUNIV UTAH RES FOUND·Filed 1994·Granted Jun 9, 1998·20 cites·9 claims
- 0846US10358678B2Methods for identifying subjects with a genetic risk for developing IgA nephropathyGHARAVI ALI·Filed 2017·Granted Jul 23, 2019·0 cites·7 claims
- 0946US2011118135A1Mutations in Contaction Associated Protein 2 (CNTNAP2) are Associated with Increased Risk for Ideopathic AutismSTATE MATTHEW W·Filed 2009·Application pending·0 cites
- 1045US9598733B2Methods for identifying subjects with a genetic risk for developing IgA nephropathyGHARVARI ALI·Filed 2012·Granted Mar 21, 2017·0 cites·2 claims
- 1143US2003082720A1Compositions methods and kits relating to treating and diagnosing hypertensionFiled 2002·Application pending·0 cites
- 1242US2017067109A1Assays for Detecting WDR62 MutationsUNIV YALE·Filed 2016·Application pending·0 cites
- 1341US11484543B2Compositions and methods for diagnosing and treating diseases and disorders associated with mutant KCNJ5UNIV ROCKEFELLER·Filed 2018·Granted Nov 1, 2022·0 cites·16 claims
- 1441US5998145AMethod to determine predisposition to hypertensionUNIV OF UTAH RESEARCH FOUNDATI·Filed 1998·Granted Dec 7, 1999·4 cites·9 claims
- 1540US9982026B2Compositions and methods for assessing and treating adrenal diseases and disordersLIFTON RICHARD P·Filed 2012·Granted May 29, 2018·0 cites·6 claims
- 1638US9464323B2Assays for detecting WDR62 mutationsGUNEL MURAT·Filed 2011·Granted Oct 11, 2016·0 cites·20 claims
- 1732US5529900ADirect genetic test for glucocorticoid-remediable aldosteronismBRIGHAM & WOMENS HOSPITAL·Filed 1993·Granted Jun 25, 1996·2 cites·8 claims
- 1832US2015044239A1Compositions and Methods for Diagnosing, Preventing and Treating Intracranial AneurysmsLIFTON RICHARD·Filed 2012·Application pending·0 cites
- 1924US6551775B1Method to diagnose and treat pathological conditions resulting from deficient ion transport such as pseudohypoaldosteronism type-1UNIV YALE·Filed 1998·Granted Apr 22, 2003·2 cites·6 claims
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Identity basis: PatentsView inventor disambiguation (2025Q4-odp release). How scoring works →